<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl13608</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-13608</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Клиническая эндокринология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Clinical endocrinology</subject></subj-group></article-categories><title-group><article-title>Феохромоцитома при нейрофиброматозе 1 типа</article-title><trans-title-group xml:lang="en"><trans-title>Pheochromocytoma in Neurofibromatosis Type 1</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7840-4174</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Реброва</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Rebrova</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Реброва Дина Владимировна - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Dina V. Rebrova - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">endocrinology@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2484-4895</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Логинова</surname><given-names>О. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Loginova</surname><given-names>O. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Логинова Ольга Ивановна,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Olga I. Loginova - MD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">olga7.smirnova@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4897-6144</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Непомнящая</surname><given-names>С. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Nepomnyashchaya</surname><given-names>S. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Непомнящая Светлана Леонидовна - к.м.н., доцент,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Svetlana L. Nepomnyashchaya - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">nsmapo@inbox.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5531-423X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бахтиярова</surname><given-names>А. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Bakhtiyarova</surname><given-names>A. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бахтиярова Алюза Рамильевна, 190103, Санкт-Петербург, набережная реки Фонтанки, д. 154;</p><p> </p><p> </p></bio><bio xml:lang="en"><p>Alyuza R. Bakhtiyarova - MD, 154 Fontanka river embankment, 190103, Saint Petersburg</p><p> </p></bio><email xlink:type="simple">alyuza_endo@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6807-778X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Русаков</surname><given-names>В. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Rusakov</surname><given-names>V. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Русаков Владимир Федорович - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Vladimir F. Rusakov - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">rusvf@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4449-0251</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Краснов</surname><given-names>Л. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasnov</surname><given-names>L. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Краснов Леонид Михайлович - д.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Leonid M. Krasnov - MD, DSc Med,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">krasnov.surg@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1294-811X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Федоров</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Fedorov</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Федоров Елисей Александрович, к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Elisey A. Fedorov - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">elick@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6986-1034</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чинчук</surname><given-names>И. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Chinchuk</surname><given-names>I. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Чинчук Игорь Константинович - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Igor K. Chinchuk - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">dr.chinchuk@bk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3876-6306</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шихмагомедов</surname><given-names>Ш. Ш.</given-names></name><name name-style="western" xml:lang="en"><surname>Shikhmagomedov</surname><given-names>Sh. Sh.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шихмагомедов Шамиль Шамсутдинович,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Shamil S. Shikhmagomedov - MD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">shihmagomedov@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4529-7891</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Имянитов</surname><given-names>Е. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Imyanitov</surname><given-names>E. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Имянитов Евгений Наумович - д.м.н., чл.-корр. РАН, </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Evgeny N. Imyanitov - MD, DSc Med, Corresponding Member of RAS,</p><p>Saint Petersburg</p></bio><email xlink:type="simple">evgeny@imyanitov.spb.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5177-2527</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кулешов</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuleshov</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кулешов Олег Владимирович - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Mikhail A. Alekseev - MD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">dkov2001@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5643-5204</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Алексеев</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Alekseev</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Алексеев Михаил Александрович,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Oleg V. Kuleshov - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">miha_decor@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7056-5977</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Придвижкина</surname><given-names>Т. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Pridvijkina</surname><given-names>T. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Придвижкина Татьяна Сергеевна - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Tatjana S. Pridvizhkina - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">pts1971@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2846-4056</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савельева</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Savelyeva</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Савельева Татьяна Вячеславовна, к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Tatyana V. Savelyeva - MD, PhD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">taleon76@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6760-0025</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Семенов</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Semenov</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Семенов Арсений Андреевич - к.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">arseny@thyro.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3500-2826</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Згода</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Zgoda</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Згода Екатерина Александровна,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Ekaterina A. Zgoda - MD,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">kateryna.zgoda@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3001-664X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черников</surname><given-names>Р. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Chernikov</surname><given-names>R. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Черников Роман Анатольевич - д.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Roman A. Chernikov - MD, DSc Med,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">yaddd@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1903-5081</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Слепцов</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sleptsov</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Слепцов Илья Валерьевич - д.м.н.,</p><p>190103, Санкт-Петербург, набережная реки Фонтанки, д. 154</p></bio><bio xml:lang="en"><p>Ilya V. Sleptsov - MD, DSc Med,</p><p>154 Fontanka river embankment, 190103, Saint Petersburg</p></bio><email xlink:type="simple">newsurgery@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Санкт-Петербургский государственный университет, Клиника высоких медицинских технологий им. Н.И. Пирогова<country>Россия</country></aff><aff xml:lang="en">Saint Petersburg State University, Saint Petersburg State University Hospital<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Санкт-Петербургский государственный университет, Клиника высоких медицинских технологий им. Н.И. Пирогова;&#13;
Национальный медицинский исследовательский центр им. В.А. Алмазова<country>Россия</country></aff><aff xml:lang="en">Saint Petersburg State University, Saint Petersburg State University Hospital;&#13;
Almazov National Medical Research Center<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">Национальный медицинский исследовательский центр онкологии им. Н.Н. Петрова<country>Россия</country></aff><aff xml:lang="en">National Medical Research Center of Oncology n.a. N.N. Petrov<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>07</day><month>03</month><year>2026</year></pub-date><volume>72</volume><issue>1</issue><fpage>69</fpage><lpage>79</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Реброва Д.В., Логинова О.И., Непомнящая С.Л., Бахтиярова А.Р., Русаков В.Ф., Краснов Л.М., Федоров Е.А., Чинчук И.К., Шихмагомедов Ш.Ш., Имянитов Е.Н., Кулешов О.В., Алексеев М.А., Придвижкина Т.С., Савельева Т.В., Семенов А.А., Згода Е.А., Черников Р.А., Слепцов И.В., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Реброва Д.В., Логинова О.И., Непомнящая С.Л., Бахтиярова А.Р., Русаков В.Ф., Краснов Л.М., Федоров Е.А., Чинчук И.К., Шихмагомедов Ш.Ш., Имянитов Е.Н., Кулешов О.В., Алексеев М.А., Придвижкина Т.С., Савельева Т.В., Семенов А.А., Згода Е.А., Черников Р.А., Слепцов И.В.</copyright-holder><copyright-holder xml:lang="en">Rebrova D.V., Loginova O.I., Nepomnyashchaya S.L., Bakhtiyarova A.R., Rusakov V.F., Krasnov L.M., Fedorov E.A., Chinchuk I.K., Shikhmagomedov S.S., Imyanitov E.N., Kuleshov O.V., Alekseev M.A., Pridvijkina T.S., Savelyeva T.V., Semenov A.A., Zgoda E.A., Chernikov R.A., Sleptsov I.V.</copyright-holder><license license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.probl-endojournals.ru/jour/article/view/13608">https://www.probl-endojournals.ru/jour/article/view/13608</self-uri><abstract><p>Нейрофиброматоз 1 типа — наследственное заболевание с широкой вариабельностью клинических проявлений, от практически полного отсутствия типичных симптомов до мультисистемного поражения организма. Одним из возможных клинических проявлений данной патологии является феохромоцитома — опухоль надпочечника с возможным развитием грозных осложнений со стороны сердечно-сосудистой системы. В статье представлено описание четырех случаев пациентов с феохромоцитомой в составе семейного нейрофиброматоза 1 типа, различающихся по клиническому течению от бессимптомной формы до ярких пароксизмальных проявлений. При этом наличие и степень артериальной гипертензии не коррелировали с уровнем метанефринов и размерами феохромоцитомы. У трех из четырех пациентов установлен наследственный анамнез нейрофиброматоза 1 типа. В одном из четырех случаев отмечалось симультанное двустороннее поражение надпочечников, при этом лучевые характеристики феохромоцитом, как при компьютерной томографии, так и при КТ/ПЭТ с 18-ФДГ, отличались от «классических». Объективный осмотр с выявлением «стертых» признаков нейрофиброматоза 1 типа позволили установить диагноз двусторонней феохромоцитомы даже при сомнительных лабораторных и визуализирующих данных. Знание клинических проявлений, своевременная диагностика нейрофиброматоза 1 типа, комплексное лечение и последующее регулярное наблюдение пациентов, а также обследование кровных родственников позволяют в значительной степени улучшить прогноз и выживаемость.</p></abstract><trans-abstract xml:lang="en"><p>Neurofibromatosis type 1 is a hereditary disease with a wide variability of clinical manifestations, from the almost complete absence of typical symptoms to a multisystem lesion of the body. One of the possible clinical manifestations of this pathology is a pheochromocytoma — a tumor of the adrenal gland with the possible development of considerable cardiovascular complications. The article describes four cases of patients with pheochromocytoma as part of familial neurofibromatosis type 1, differing in clinical course from asymptomatic form to vivid paroxysmal manifestations. At the same time, the presence and degree of arterial hypertension did not correlate with the level of metanephrines and the size of the pheochromocytoma. 3 out of 4 patients have a hereditary history of neurofibromatosis type 1. In 1 out of 4 cases, simultaneous bilateral damage to the adrenal glands was noted, while the radiation characteristics of pheochromocytomas, both with computed tomography and CT/PET with 18-FDG, differed from the "classic" ones. An objective examination with the identification of "erased" signs of neurofibromatosis type 1 made it possible to establish the diagnosis of bilateral pheochromocytoma even with questionable laboratory and imaging data. Knowledge of clinical manifestations, timely diagnosis of neurofibromatosis type 1, comprehensive treatment and subsequent regular monitoring of patients, as well as examination of blood relatives can significantly improve prognosis and survival.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>новообразование надпочечника</kwd><kwd>инциденталома надпочечника</kwd><kwd>феохромоцитома</kwd><kwd>болезнь Реклингхаузена</kwd><kwd>нейрофиброматоз 1 типа</kwd></kwd-group><kwd-group xml:lang="en"><kwd>adrenal tumor</kwd><kwd>adrenal incidentaloma</kwd><kwd>pheochromocytoma</kwd><kwd>Recklinghausen’s disease</kwd><kwd>neurofibromatosis type 1</kwd></kwd-group></article-meta></front><back><ref-list><ref id="cit1"><element-citation><name><surname>Williams</surname> <given-names>Virginia C.</given-names> </name> <name><surname>Lucas</surname> <given-names>John</given-names> </name> <name><surname>Babcock</surname> <given-names>Michael A.</given-names> </name> <name><surname>Gutmann</surname> <given-names>David H.</given-names> </name> <name><surname>Korf</surname> <given-names>Bruce</given-names> </name> <name><surname>Maria</surname> <given-names>Bernard L.</given-names> </name> <article-title>Neurofibromatosis Type 1 Revisited</article-title> <source>Pediatrics</source> <year>2008</year> <month>12</month> <fpage>124</fpage> <lpage>133</lpage> <volume>123</volume> <issue>1</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1542/peds.2007-3204</object-id></element-citation></ref><ref id="cit2"><element-citation><name><surname>Stewart</surname> <given-names>Douglas R.</given-names> </name> <name><surname>Korf</surname> <given-names>Bruce R.</given-names> </name> <name><surname>Nathanson</surname> <given-names>Katherine L.</given-names> </name> <name><surname>Stevenson</surname> <given-names>David A.</given-names> </name> <name><surname>Yohay</surname> <given-names>Kaleb</given-names> </name> <article-title>Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)</article-title> <source>Genetics in Medicine</source> <year>2018</year> <month>04</month> <fpage>671</fpage> <lpage>682</lpage> <volume>20</volume> <issue>7</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1038/gim.2018.28</object-id></element-citation></ref><ref id="cit3"><mixed-citation publication-type="commun" publication-format="web"><name><surname>Miraglia</surname> <given-names>E</given-names></name>, <name><surname>Moliterni</surname> <given-names>E</given-names></name>, <name><surname>Iacovino</surname> <given-names>C</given-names></name>, et al. <article-title>Cutaneous manifestations in neurofibromatosis type 1.</article-title> <source>Clin Ter.</source> <year>2020</year>;<issue>171(5)</issue>:<fpage>e371</fpage>-<lpage>e377</lpage>. doi: https://doi.org/<object-id pub-id-type="doi" specific-use="metadata">10.7417/CT.2020.2242</object-id></mixed-citation></ref><ref id="cit4"><element-citation><name><surname>Shofty</surname> <given-names>Ben</given-names> </name> <name><surname>Barzilai</surname> <given-names>Ori</given-names> </name> <name><surname>Khashan</surname> <given-names>Morsi</given-names> </name> <name><surname>Lidar</surname> <given-names>Zvi</given-names> </name> <name><surname>Constantini</surname> <given-names>Shlomi</given-names> </name> <article-title>Spinal manifestations of Neurofibromatosis type 1</article-title> <source>Child's Nervous System</source> <year>2020</year> <month>06</month> <fpage>2401</fpage> <lpage>2408</lpage> <volume>36</volume> <issue>10</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s00381-020-04754-9</object-id></element-citation></ref><ref id="cit5"><element-citation><name><surname>Yukina</surname> <given-names>M. Yu.</given-names> </name> <name><surname>Avsievich</surname> <given-names>E. S.</given-names> </name> <name><surname>Pushkareva</surname> <given-names>A. S.</given-names> </name> <name><surname>Nuralieva</surname> <given-names>N. F.</given-names> </name> <name><surname>Bondarenko</surname> <given-names>E. V.</given-names> </name> <name><surname>Platonova</surname> <given-names>N. M.</given-names> </name> <name><surname>Beltsevich</surname> <given-names>D. G.</given-names> </name> <name><surname>Troshina</surname> <given-names>E. A.</given-names> </name> <article-title>Atypical and typical course of neurofibromatosis type 1 in combination with pheochromocytoma</article-title> <source>Endocrine Surgery</source> <year>2022</year> <month>12</month> <fpage>30</fpage> <lpage>40</lpage> <volume>15</volume> <issue>3</issue> <object-id pub-id-type="doi" specific-use="metadata">10.14341/serg12730</object-id></element-citation></ref><ref id="cit6"><element-citation><name><surname>Gutmann</surname> <given-names>David H.</given-names> </name> <name><surname>Ferner</surname> <given-names>Rosalie E.</given-names> </name> <name><surname>Listernick</surname> <given-names>Robert H.</given-names> </name> <name><surname>Korf</surname> <given-names>Bruce R.</given-names> </name> <name><surname>Wolters</surname> <given-names>Pamela L.</given-names> </name> <name><surname>Johnson</surname> <given-names>Kimberly J.</given-names> </name> <article-title>Neurofibromatosis type 1</article-title> <source>Nature Reviews Disease Primers</source> <year>2017</year> <month>02</month> <volume>3</volume> <issue>1</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1038/nrdp.2017.4</object-id></element-citation></ref><ref id="cit7"><element-citation><name><surname>Rebrova</surname> <given-names>D. V.</given-names> </name> <name><surname>Vorokhobina</surname> <given-names>N. V.</given-names> </name> <name><surname>Imyanitov</surname> <given-names>E. N.</given-names> </name> <name><surname>Rusakov</surname> <given-names>V F.</given-names> </name> <name><surname>Krasnov</surname> <given-names>L. M.</given-names> </name> <name><surname>Sleptsov</surname> <given-names>I. V.</given-names> </name> <name><surname>Chernikov</surname> <given-names>R. A.</given-names> </name> <name><surname>Fedorov</surname> <given-names>E. A.</given-names> </name> <name><surname>Semenov</surname> <given-names>A. A.</given-names> </name> <name><surname>Chinchuk</surname> <given-names>I. K.</given-names> </name> <name><surname>Sablin</surname> <given-names>I. V.</given-names> </name> <name><surname>Alekseev</surname> <given-names>M. A.</given-names> </name> <name><surname>Kuleshov</surname> <given-names>O. V.</given-names> </name> <name><surname>Fedotov</surname> <given-names>Ju. N</given-names> </name> <article-title>Clinical and laboratory features of hereditary pheochromocytoma and paraganglioma</article-title> <source>Problems of Endocrinology</source> <year>2022</year> <month>03</month> <fpage>8</fpage> <lpage>17</lpage> <volume>68</volume> <issue>1</issue> <object-id pub-id-type="doi" specific-use="metadata">10.14341/probl12834</object-id></element-citation></ref><ref id="cit8"><element-citation><name><surname>Saleh</surname> <given-names>Mustafa</given-names> </name> <name><surname>Dib</surname> <given-names>AlFadel</given-names> </name> <name><surname>Beaini</surname> <given-names>Sarah</given-names> </name> <name><surname>Saad</surname> <given-names>Charbel</given-names> </name> <name><surname>Faraj</surname> <given-names>Sary</given-names> </name> <name><surname>El Joueid</surname> <given-names>Youssef</given-names> </name> <name><surname>Kotob</surname> <given-names>Yasmine</given-names> </name> <name><surname>Saoudi</surname> <given-names>Lara</given-names> </name> <name><surname>Emmanuel</surname> <given-names>Nancy</given-names> </name> <article-title>Neurofibromatosis type 1 system-based manifestations and treatments: a review</article-title> <source>Neurological Sciences</source> <year>2023</year> <month>02</month> <fpage>1931</fpage> <lpage>1947</lpage> <volume>44</volume> <issue>6</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s10072-023-06680-5</object-id></element-citation></ref><ref id="cit9"><element-citation><article-title>Neurofibromatosis type 1</article-title> <source>Handbook of Clinical Neurology</source> <year>2015</year> <month>11</month> <fpage>75</fpage> <lpage>86</lpage> <object-id pub-id-type="doi" specific-use="metadata">10.1016/b978-0-444-62702-5.00004-4</object-id></element-citation></ref><ref id="cit10"><element-citation><name><surname>Aronow</surname> <given-names>Mary E.</given-names> </name> <name><surname>Wiley</surname> <given-names>Henry E.</given-names> </name> <name><surname>Gaudric</surname> <given-names>Alain</given-names> </name> <name><surname>Krivosic</surname> <given-names>Valerie</given-names> </name> <name><surname>Gorin</surname> <given-names>Michael B.</given-names> </name> <name><surname>Shields</surname> <given-names>Carol L.</given-names> </name> <name><surname>Shields</surname> <given-names>Jerry A.</given-names> </name> <name><surname>Jonasch</surname> <given-names>Eric W.</given-names> </name> <name><surname>Singh</surname> <given-names>Arun D.</given-names> </name> <name><surname>Chew</surname> <given-names>Emily Y.</given-names> </name> <article-title>VON HIPPEL–LINDAU DISEASE</article-title> <source>Retina</source> <year>2019</year> <month>05</month> <fpage>2243</fpage> <lpage>2253</lpage> <volume>39</volume> <issue>12</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1097/iae.0000000000002555</object-id></element-citation></ref><ref id="cit11"><element-citation><name><surname>Kehrer-Sawatzki</surname> <given-names>Hildegard</given-names> </name> <name><surname>Cooper</surname> <given-names>David N.</given-names> </name> <article-title>Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants</article-title> <source>Human Genetics</source> <year>2021</year> <month>12</month> <fpage>177</fpage> <lpage>191</lpage> <volume>141</volume> <issue>2</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s00439-021-02410-z</object-id></element-citation></ref><ref id="cit12"><mixed-citation publication-type="commun" publication-format="web"><name><surname>Mel'nichenko</surname> <given-names>G.A.</given-names></name> i soavt. <article-title>Klinicheskie rekomendatsii Rossiiskoi assotsiatsii endokrinologov po diagnostike i lecheniyu feokhromotsitomy/paragangliomy.</article-title> // <source>Endokrinnaya khirurgiya.</source> — <year>2015</year>. — T.<volume>9</volume>. — №<month>3</month>. — S.<fpage>15</fpage>-<lpage>33</lpage>. doi: https://doi.org/<object-id pub-id-type="doi" specific-use="metadata">10.14341/serg201531533</object-id></mixed-citation></ref><ref id="cit13"><element-citation><name><surname>Garcia-Carbonero</surname> <given-names>R.</given-names> </name> <name><surname>Matute Teresa</surname> <given-names>F.</given-names> </name> <name><surname>Mercader-Cidoncha</surname> <given-names>E.</given-names> </name> <name><surname>Mitjavila-Casanovas</surname> <given-names>M.</given-names> </name> <name><surname>Robledo</surname> <given-names>M.</given-names> </name> <name><surname>Tena</surname> <given-names>I.</given-names> </name> <name><surname>Alvarez-Escola</surname> <given-names>C.</given-names> </name> <name><surname>Arístegui</surname> <given-names>M.</given-names> </name> <name><surname>Bella-Cueto</surname> <given-names>M. R.</given-names> </name> <name><surname>Ferrer-Albiach</surname> <given-names>C.</given-names> </name> <name><surname>Hanzu</surname> <given-names>F. A.</given-names> </name> <article-title>Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas</article-title> <source>Clinical and Translational Oncology</source> <year>2021</year> <month>05</month> <fpage>1995</fpage> <lpage>2019</lpage> <volume>23</volume> <issue>10</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s12094-021-02622-9</object-id></element-citation></ref><ref id="cit14"><element-citation><name><surname>Loponen</surname> <given-names>Niina</given-names> </name> <name><surname>Ylä‐Outinen</surname> <given-names>Heli</given-names> </name> <name><surname>Kallionpää</surname> <given-names>Roope A.</given-names> </name> <name><surname>Valtanen</surname> <given-names>Mikko</given-names> </name> <name><surname>Auranen</surname> <given-names>Kari</given-names> </name> <name><surname>Järveläinen</surname> <given-names>Hannu</given-names> </name> <name><surname>Peltonen</surname> <given-names>Sirkku</given-names> </name> <name><surname>Peltonen</surname> <given-names>Juha</given-names> </name> <article-title>Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes</article-title> <source>Molecular Genetics &amp; Genomic Medicine</source> <year>2023</year> <month>12</month> <volume>12</volume> <issue>1</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1002/mgg3.2346</object-id></element-citation></ref><ref id="cit15"><element-citation><name><surname>Zinnamosca</surname> <given-names>Laura</given-names> </name> <name><surname>Petramala</surname> <given-names>Luigi</given-names> </name> <name><surname>Cotesta</surname> <given-names>Dario</given-names> </name> <name><surname>Marinelli</surname> <given-names>Cristiano</given-names> </name> <name><surname>Schina</surname> <given-names>Mauro</given-names> </name> <name><surname>Cianci</surname> <given-names>Rosario</given-names> </name> <name><surname>Giustini</surname> <given-names>Sandra</given-names> </name> <name><surname>Sciomer</surname> <given-names>Susanna</given-names> </name> <name><surname>Anastasi</surname> <given-names>Emanuela</given-names> </name> <name><surname>Calvieri</surname> <given-names>Stefano</given-names> </name> <name><surname>De Toma</surname> <given-names>Giorgio</given-names> </name> <name><surname>Letizia</surname> <given-names>Claudio</given-names> </name> <article-title>Neurofibromatosis type 1 (NF1) and pheochromocytoma: prevalence, clinical and cardiovascular aspects</article-title> <source>Archives of Dermatological Research</source> <year>2010</year> <month>11</month> <fpage>317</fpage> <lpage>325</lpage> <volume>303</volume> <issue>5</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s00403-010-1090-z</object-id></element-citation></ref><ref id="cit16"><element-citation><name><surname>Tachibana</surname> <given-names>Akira</given-names> </name> <name><surname>Iida</surname> <given-names>Kota</given-names> </name> <name><surname>Itami</surname> <given-names>Yoshitaka</given-names> </name> <name><surname>Hashimura</surname> <given-names>Masaya</given-names> </name> <name><surname>Hosokawa</surname> <given-names>Yukinari</given-names> </name> <name><surname>Fujimoto</surname> <given-names>Kiyohide</given-names> </name> <article-title>Composite pheochromocytoma associated with neurofibromatosis type 1</article-title> <source>IJU Case Reports</source> <year>2023</year> <month>06</month> <fpage>278</fpage> <lpage>281</lpage> <volume>6</volume> <issue>5</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1002/iju5.12603</object-id></element-citation></ref><ref id="cit17"><element-citation><name><surname>Dupuis</surname> <given-names>Hippolyte</given-names> </name> <name><surname>Chevalier</surname> <given-names>Benjamin</given-names> </name> <name><surname>Cardot-Bauters</surname> <given-names>Catherine</given-names> </name> <name><surname>Jannin</surname> <given-names>Arnaud</given-names> </name> <name><surname>Do Cao</surname> <given-names>Christine</given-names> </name> <name><surname>Ladsous</surname> <given-names>Miriam</given-names> </name> <name><surname>Cortet</surname> <given-names>Christine</given-names> </name> <name><surname>Merlen</surname> <given-names>Emilie</given-names> </name> <name><surname>Drouard</surname> <given-names>Magali</given-names> </name> <name><surname>Aubert</surname> <given-names>Sébastien</given-names> </name> <name><surname>Vidaud</surname> <given-names>Dominique</given-names> </name> <name><surname>Espiard</surname> <given-names>Stéphanie</given-names> </name> <name><surname>Vantyghem</surname> <given-names>Marie-Christine</given-names> </name> <article-title>Prevalence of Endocrine Manifestations and GIST in 108 Systematically Screened Patients With Neurofibromatosis Type 1</article-title> <source>Journal of the Endocrine Society</source> <year>2023</year> <month>06</month> <volume>7</volume> <issue>8</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1210/jendso/bvad083</object-id></element-citation></ref><ref id="cit18"><element-citation><name><surname>Képénékian</surname> <given-names>Lori</given-names> </name> <name><surname>Mognetti</surname> <given-names>Thomas</given-names> </name> <name><surname>Lifante</surname> <given-names>Jean-Christophe</given-names> </name> <name><surname>Giraudet</surname> <given-names>Anne-Laure</given-names> </name> <name><surname>Houzard</surname> <given-names>Claire</given-names> </name> <name><surname>Pinson</surname> <given-names>Stéphane</given-names> </name> <name><surname>Borson-Chazot</surname> <given-names>Françoise</given-names> </name> <name><surname>Combemale</surname> <given-names>Patrick</given-names> </name> <article-title>Interest of systematic screening of pheochromocytoma in patients with neurofibromatosis type 1</article-title> <source>European Journal of Endocrinology</source> <year>2016</year> <month>07</month> <fpage>335</fpage> <lpage>344</lpage> <volume>175</volume> <issue>4</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1530/eje-16-0233</object-id></element-citation></ref><ref id="cit19"><element-citation><name><surname>Kiriakopoulos</surname> <given-names>Andreas</given-names> </name> <name><surname>Giannakis</surname> <given-names>Periklis</given-names> </name> <name><surname>Menenakos</surname> <given-names>Evangelos</given-names> </name> <article-title>Pheochromocytoma: a changing perspective and current concepts</article-title> <source>Therapeutic Advances in Endocrinology and Metabolism</source> <year>2023</year> <month>10</month> <volume>14</volume> <object-id pub-id-type="doi" specific-use="metadata">10.1177/20420188231207544</object-id></element-citation></ref><ref id="cit20"><element-citation><name><surname>Farias</surname> <given-names>Francisco</given-names> </name> <name><surname>Yogeswaran</surname> <given-names>Vidhushei</given-names> </name> <name><surname>Hidano</surname> <given-names>Danelle</given-names> </name> <name><surname>Starnes</surname> <given-names>Elizabeth</given-names> </name> <name><surname>Kwon</surname> <given-names>Young</given-names> </name> <name><surname>Branch</surname> <given-names>Kelley</given-names> </name> <name><surname>Tylee</surname> <given-names>Tracy</given-names> </name> <name><surname>Poole</surname> <given-names>Jeanne</given-names> </name> <name><surname>Sridhar</surname> <given-names>Arun</given-names> </name> <article-title>Ventricular fibrillation due to pheochromocytoma crisis in a previously asymptomatic patient</article-title> <source>Journal of Cardiology Cases</source> <year>2023</year> <month>03</month> <fpage>222</fpage> <lpage>225</lpage> <volume>27</volume> <issue>5</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1016/j.jccase.2023.02.011</object-id></element-citation></ref><ref id="cit21"><element-citation><name><surname>Petr</surname> <given-names>Elisabeth Joye</given-names> </name> <name><surname>Else</surname> <given-names>Tobias</given-names> </name> <article-title>Pheochromocytoma and Paraganglioma in Neurofibromatosis type 1: frequent surgeries and cardiovascular crises indicate the need for screening</article-title> <source>Clinical Diabetes and Endocrinology</source> <year>2018</year> <month>06</month> <volume>4</volume> <issue>1</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1186/s40842-018-0065-4</object-id></element-citation></ref><ref id="cit22"><mixed-citation publication-type="commun" publication-format="web"><name><surname>Bausch</surname> <given-names>B.</given-names></name>, <name><surname>Borozdin</surname> <given-names>W.</given-names></name>, <name><surname>Neumann</surname> <given-names>H.P.</given-names></name> <article-title>Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma.</article-title> <source>N Engl J Med.</source> <year>2006</year>;<issue>354(25)</issue>:<fpage>2729</fpage>–<lpage>2731</lpage></mixed-citation></ref><ref id="cit23"><element-citation><name><surname>Carton</surname> <given-names>Charlotte</given-names> </name> <name><surname>Evans</surname> <given-names>D. Gareth</given-names> </name> <name><surname>Blanco</surname> <given-names>Ignacio</given-names> </name> <name><surname>Friedrich</surname> <given-names>Reinhard E.</given-names> </name> <name><surname>Ferner</surname> <given-names>Rosalie E.</given-names> </name> <name><surname>Farschtschi</surname> <given-names>Said</given-names> </name> <name><surname>Salvador</surname> <given-names>Hector</given-names> </name> <name><surname>Azizi</surname> <given-names>Amedeo A.</given-names> </name> <name><surname>Mautner</surname> <given-names>Victor</given-names> </name> <name><surname>Röhl</surname> <given-names>Claas</given-names> </name> <name><surname>Peltonen</surname> <given-names>Sirkku</given-names> </name> <name><surname>Stivaros</surname> <given-names>Stavros</given-names> </name> <name><surname>Legius</surname> <given-names>Eric</given-names> </name> <name><surname>Oostenbrink</surname> <given-names>Rianne</given-names> </name> <name><surname>Brunet</surname> <given-names>Joan</given-names> </name> <name><surname>Van Calenbergh</surname> <given-names>Frank</given-names> </name> <name><surname>Cassiman</surname> <given-names>Catherine</given-names> </name> <name><surname>Czech</surname> <given-names>Thomas</given-names> </name> <name><surname>Gavarrete de León</surname> <given-names>María José</given-names> </name> <name><surname>Giele</surname> <given-names>Henk</given-names> </name> <name><surname>Henley</surname> <given-names>Susie</given-names> </name> <name><surname>Lazaro</surname> <given-names>Conxi</given-names> </name> <name><surname>Lipkovskaya</surname> <given-names>Vera</given-names> </name> <name><surname>Maher</surname> <given-names>Eamonn R.</given-names> </name> <name><surname>Martin</surname> <given-names>Vanessa</given-names> </name> <name><surname>Mathijssen</surname> <given-names>Irene</given-names> </name> <name><surname>Opocher</surname> <given-names>Enrico</given-names> </name> <name><surname>Pires</surname> <given-names>Ana Elisabete</given-names> </name> <name><surname>Pletschko</surname> <given-names>Thomas</given-names> </name> <name><surname>Poupaki</surname> <given-names>Eirene</given-names> </name> <name><surname>Ridola</surname> <given-names>Vita</given-names> </name> <name><surname>Rietman</surname> <given-names>Andre</given-names> </name> <name><surname>Rosenbaum</surname> <given-names>Thorsten</given-names> </name> <name><surname>Santhouse</surname> <given-names>Alastair</given-names> </name> <name><surname>Sehested</surname> <given-names>Astrid</given-names> </name> <name><surname>Simmons</surname> <given-names>Ian</given-names> </name> <name><surname>Taal</surname> <given-names>Walter</given-names> </name> <name><surname>Wagner</surname> <given-names>Anja</given-names> </name> <article-title>ERN GENTURIS tumour surveillance guidelines for individuals with neurofibromatosis type 1</article-title> <source>eClinicalMedicine</source> <year>2023</year> <month>01</month> <fpage>101818</fpage> <volume>56</volume> <object-id pub-id-type="doi" specific-use="metadata">10.1016/j.eclinm.2022.101818</object-id></element-citation></ref><ref id="cit24"><element-citation><name><surname>Buffet</surname> <given-names>Alexandre</given-names> </name> <name><surname>Burnichon</surname> <given-names>Nelly</given-names> </name> <name><surname>Favier</surname> <given-names>Judith</given-names> </name> <name><surname>Gimenez-Roqueplo</surname> <given-names>Anne-Paule</given-names> </name> <article-title>An overview of 20 years of genetic studies in pheochromocytoma and paraganglioma</article-title> <source>Best Practice &amp; Research Clinical Endocrinology &amp; Metabolism</source> <year>2020</year> <month>03</month> <fpage>101416</fpage> <volume>34</volume> <issue>2</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1016/j.beem.2020.101416</object-id></element-citation></ref><ref id="cit25"><element-citation><name><surname>Shinall</surname> <given-names>Myrick C</given-names> </name> <name><surname>Solórzano</surname> <given-names>Carmen C</given-names> </name> <article-title>Pheochromocytoma in Neurofibromatosis Type 1: When Should it Be Suspected</article-title> <source>Endocrine Practice</source> <year>2014</year> <month>02</month> <fpage>792</fpage> <lpage>796</lpage> <volume>20</volume> <issue>8</issue> <object-id pub-id-type="doi" specific-use="metadata">10.4158/ep13417.or</object-id></element-citation></ref><ref id="cit26"><element-citation><name><surname>Lider Burciulescu</surname> <given-names>Sofia Maria</given-names> </name> <name><surname>Gheorghiu</surname> <given-names>Monica Livia</given-names> </name> <name><surname>Muresan</surname> <given-names>Andrei</given-names> </name> <name><surname>Gherlan</surname> <given-names>Iuliana</given-names> </name> <name><surname>Patocs</surname> <given-names>Attila</given-names> </name> <name><surname>Badiu</surname> <given-names>Corin</given-names> </name> <article-title>Bilateral pheochromocytomas: clinical presentation and morbidity rate related to surgery technique and genetic status</article-title> <source>Endocrine Connections</source> <year>2024</year> <month>02</month> <volume>13</volume> <issue>4</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1530/ec-23-0466</object-id></element-citation></ref><ref id="cit27"><element-citation><name><surname>Shikhmagomedov</surname> <given-names>Sh. Sh.</given-names> </name> <name><surname>Rebrova</surname> <given-names>D. V.</given-names> </name> <name><surname>Krasnov</surname> <given-names>L. M.</given-names> </name> <name><surname>Fedorov</surname> <given-names>E. A.</given-names> </name> <name><surname>Chinchuk</surname> <given-names>I. K.</given-names> </name> <name><surname>Chernikov</surname> <given-names>R. A.</given-names> </name> <name><surname>Rusakov</surname> <given-names>V. F.</given-names> </name> <name><surname>Slepstov</surname> <given-names>I. V.</given-names> </name> <name><surname>Zgoda</surname> <given-names>E. A.</given-names> </name> <article-title>Surgical treatment of pheochromocytoma</article-title> <source>Problems of Endocrinology</source> <year>2023</year> <month>11</month> <fpage>39</fpage> <lpage>44</lpage> <volume>69</volume> <issue>5</issue> <object-id pub-id-type="doi" specific-use="metadata">10.14341/probl13283</object-id></element-citation></ref><ref id="cit28"><element-citation><name><surname>Walz</surname> <given-names>Martin K.</given-names> </name> <name><surname>Alesina</surname> <given-names>Piero F.</given-names> </name> <name><surname>Wenger</surname> <given-names>Frank A.</given-names> </name> <name><surname>Deligiannis</surname> <given-names>Anastasios</given-names> </name> <name><surname>Szuczik</surname> <given-names>Eduard</given-names> </name> <name><surname>Petersenn</surname> <given-names>Stephan</given-names> </name> <name><surname>Ommer</surname> <given-names>Andreas</given-names> </name> <name><surname>Groeben</surname> <given-names>Harald</given-names> </name> <name><surname>Peitgen</surname> <given-names>Klaus</given-names> </name> <name><surname>Janssen</surname> <given-names>Onno E.</given-names> </name> <name><surname>Philipp</surname> <given-names>Thomas</given-names> </name> <name><surname>Neumann</surname> <given-names>Hartmut P.H.</given-names> </name> <name><surname>Schmid</surname> <given-names>Kurt W.</given-names> </name> <name><surname>Mann</surname> <given-names>Klaus</given-names> </name> <article-title>Posterior retroperitoneoscopic adrenalectomy—results of 560 procedures in 520 patients</article-title> <source>Surgery</source> <year>2006</year> <month>12</month> <fpage>943</fpage> <lpage>950</lpage> <volume>140</volume> <issue>6</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1016/j.surg.2006.07.039</object-id></element-citation></ref><ref id="cit29"><element-citation><name><surname>Shikhmagomedov</surname> <given-names>Sh. Sh.</given-names> </name> <name><surname>Rebrova</surname> <given-names>D. V.</given-names> </name> <name><surname>Alekseev</surname> <given-names>M. A.</given-names> </name> <name><surname>Krasnov</surname> <given-names>L. M.</given-names> </name> <name><surname>Fedorov</surname> <given-names>E. A.</given-names> </name> <name><surname>Chinchuk</surname> <given-names>I. K.</given-names> </name> <name><surname>Chernikov</surname> <given-names>R. A.</given-names> </name> <name><surname>Rusakov</surname> <given-names>V. F.</given-names> </name> <name><surname>Sleptsov</surname> <given-names>I. V.</given-names> </name> <name><surname>Sablin</surname> <given-names>I. V.</given-names> </name> <name><surname>Kuleshov</surname> <given-names>O. V.</given-names> </name> <article-title>Comparison of intraoperative hemodynamics in classical and single-port adrenalectomy</article-title> <source>Endocrine Surgery</source> <year>2024</year> <month>07</month> <fpage>23</fpage> <lpage>29</lpage> <volume>18</volume> <issue>2</issue> <object-id pub-id-type="doi" specific-use="metadata">10.14341/serg12837</object-id></element-citation></ref><ref id="cit30"><element-citation><name><surname>Luo</surname> <given-names>Yancheng</given-names> </name> <name><surname>Chen</surname> <given-names>Xiang</given-names> </name> <name><surname>Chen</surname> <given-names>Zhi</given-names> </name> <name><surname>He</surname> <given-names>Yao</given-names> </name> <name><surname>Li</surname> <given-names>Nannan</given-names> </name> <name><surname>Lai</surname> <given-names>Cheng</given-names> </name> <name><surname>Xie</surname> <given-names>Chaoqun</given-names> </name> <article-title>Retroperitoneal Laparoendoscopic Single-Site Adrenalectomy: Our Initial Technical Experience</article-title> <source>Journal of Laparoendoscopic &amp; Advanced Surgical Techniques</source> <year>2012</year> <month>06</month> <fpage>584</fpage> <lpage>586</lpage> <volume>22</volume> <issue>6</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1089/lap.2011.0468</object-id></element-citation></ref><ref id="cit31"><element-citation><name><surname>Neumann</surname> <given-names>Hartmut P. H.</given-names> </name> <name><surname>Tsoy</surname> <given-names>Uliana</given-names> </name> <name><surname>Bancos</surname> <given-names>Irina</given-names> </name> <name><surname>Amodru</surname> <given-names>Vincent</given-names> </name> <name><surname>Walz</surname> <given-names>Martin K.</given-names> </name> <name><surname>Tirosh</surname> <given-names>Amit</given-names> </name> <name><surname>Kaur</surname> <given-names>Ravinder Jeet</given-names> </name> <name><surname>McKenzie</surname> <given-names>Travis</given-names> </name> <name><surname>Qi</surname> <given-names>Xiaoping</given-names> </name> <name><surname>Bandgar</surname> <given-names>Tushar</given-names> </name> <name><surname>Petrov</surname> <given-names>Roman</given-names> </name> <name><surname>Yukina</surname> <given-names>Marina Y.</given-names> </name> <name><surname>Roslyakova</surname> <given-names>Anna</given-names> </name> <name><surname>van der Horst-Schrivers</surname> <given-names>Anouk N. A.</given-names> </name> <name><surname>Berends</surname> <given-names>Annika M. A.</given-names> </name> <name><surname>Hoff</surname> <given-names>Ana O.</given-names> </name> <name><surname>Castroneves</surname> <given-names>Luciana Audi</given-names> </name> <name><surname>Ferrara</surname> <given-names>Alfonso Massimiliano</given-names> </name> <name><surname>Rizzati</surname> <given-names>Silvia</given-names> </name> <name><surname>Mian</surname> <given-names>Caterina</given-names> </name> <name><surname>Dvorakova</surname> <given-names>Sarka</given-names> </name> <name><surname>Hasse-Lazar</surname> <given-names>Kornelia</given-names> </name> <name><surname>Kvachenyuk</surname> <given-names>Andrey</given-names> </name> <name><surname>Peczkowska</surname> <given-names>Mariola</given-names> </name> <name><surname>Loli</surname> <given-names>Paola</given-names> </name> <name><surname>Erenler</surname> <given-names>Feyza</given-names> </name> <name><surname>Krauss</surname> <given-names>Tobias</given-names> </name> <name><surname>Almeida</surname> <given-names>Madson Q.</given-names> </name> <name><surname>Liu</surname> <given-names>Longfei</given-names> </name> <name><surname>Zhu</surname> <given-names>Feizhou</given-names> </name> <name><surname>Recasens</surname> <given-names>Mònica</given-names> </name> <name><surname>Wohllk</surname> <given-names>Nelson</given-names> </name> <name><surname>Corssmit</surname> <given-names>Eleonora P. M.</given-names> </name> <name><surname>Shafigullina</surname> <given-names>Zulfiya</given-names> </name> <name><surname>Calissendorff</surname> <given-names>Jan</given-names> </name> <name><surname>Grozinsky-Glasberg</surname> <given-names>Simona</given-names> </name> <name><surname>Kunavisarut</surname> <given-names>Tada</given-names> </name> <name><surname>Schalin-Jäntti</surname> <given-names>Camilla</given-names> </name> <name><surname>Castinetti</surname> <given-names>Frederic</given-names> </name> <name><surname>Vlcek</surname> <given-names>Petr</given-names> </name> <name><surname>Beltsevich</surname> <given-names>Dmitry</given-names> </name> <name><surname>Egorov</surname> <given-names>Viacheslav I.</given-names> </name> <name><surname>Schiavi</surname> <given-names>Francesca</given-names> </name> <name><surname>Links</surname> <given-names>Thera P.</given-names> </name> <name><surname>Lechan</surname> <given-names>Ronald M.</given-names> </name> <name><surname>Bausch</surname> <given-names>Birke</given-names> </name> <name><surname>Young</surname> <given-names>William F.</given-names> </name> <name><surname>Eng</surname> <given-names>Charis</given-names> </name>  <article-title>Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy</article-title> <source>JAMA Network Open</source> <year>2019</year> <month>08</month> <fpage>e198898</fpage> <volume>2</volume> <issue>8</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1001/jamanetworkopen.2019.8898</object-id></element-citation></ref><ref id="cit32"><element-citation><name><surname>Zawadzka</surname> <given-names>Karolina</given-names> </name> <name><surname>Tylec</surname> <given-names>Piotr</given-names> </name> <name><surname>Małłczak</surname> <given-names>Piotr</given-names> </name> <name><surname>Major</surname> <given-names>Piotr</given-names> </name> <name><surname>Pe¸dziwiatr</surname> <given-names>Michał</given-names> </name> <name><surname>Pisarska-Adamczyk</surname> <given-names>Magdalena</given-names> </name> <article-title>Cortical-sparing adrenalectomy for bilateral pheochromocytoma - is it a game worth the candle? Systematic review with meta-analysis comparing total vs partial adrenalectomy in bilateral pheochromocytoma</article-title> <source>Endocrine Abstracts</source> <year>2022</year> <month>05</month> <object-id pub-id-type="doi" specific-use="metadata">10.1530/endoabs.81.p520</object-id></element-citation></ref><ref id="cit33"><element-citation><name><surname>Perysinakis</surname> <given-names>Iraklis</given-names> </name> <name><surname>Aggeli</surname> <given-names>Ch.</given-names> </name> <name><surname>Kaltsas</surname> <given-names>Gr.</given-names> </name> <name><surname>Zografos</surname> <given-names>G. N.</given-names> </name> <article-title>Adrenal-sparing surgery: current concepts on a theme from the past</article-title> <source>Hormones</source> <year>2020</year> <month>05</month> <fpage>317</fpage> <lpage>327</lpage> <volume>19</volume> <issue>3</issue> <object-id pub-id-type="doi" specific-use="metadata">10.1007/s42000-020-00202-0</object-id></element-citation></ref><ref id="cit34"><element-citation><name><surname>Mellid</surname> <given-names>Sara</given-names> </name> <name><surname>Gil</surname> <given-names>Eduardo</given-names> </name> <name><surname>Letón</surname> <given-names>Rocío</given-names> </name> <name><surname>Caleiras</surname> <given-names>Eduardo</given-names> </name> <name><surname>Honrado</surname> <given-names>Emiliano</given-names> </name> <name><surname>Richter</surname> <given-names>Susan</given-names> </name> <name><surname>Palacios</surname> <given-names>Nuria</given-names> </name> <name><surname>Lahera</surname> <given-names>Marcos</given-names> </name> <name><surname>Galofré</surname> <given-names>Juan C.</given-names> </name> <name><surname>López-Fernández</surname> <given-names>Adriá</given-names> </name> <name><surname>Calatayud</surname> <given-names>Maria</given-names> </name> <name><surname>Herrera-Martínez</surname> <given-names>Aura D.</given-names> </name> <name><surname>Galvez</surname> <given-names>María A.</given-names> </name> <name><surname>Matias-Guiu</surname> <given-names>Xavier</given-names> </name> <name><surname>Balbín</surname> <given-names>Milagros</given-names> </name> <name><surname>Korpershoek</surname> <given-names>Esther</given-names> </name> <name><surname>Lim</surname> <given-names>Eugénie S.</given-names> </name> <name><surname>Maletta</surname> <given-names>Francesca</given-names> </name> <name><surname>Lider</surname> <given-names>Sofia</given-names> </name> <name><surname>Fliedner</surname> <given-names>Stephanie M. J.</given-names> </name> <name><surname>Bechmann</surname> <given-names>Nicole</given-names> </name> <name><surname>Eisenhofer</surname> <given-names>Graeme</given-names> </name> <name><surname>Canu</surname> <given-names>Letizia</given-names> </name> <name><surname>Rapizzi</surname> <given-names>Elena</given-names> </name> <name><surname>Bancos</surname> <given-names>Irina</given-names> </name> <name><surname>Robledo</surname> <given-names>Mercedes</given-names> </name> <name><surname>Cascón</surname> <given-names>Alberto</given-names> </name> <article-title>Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma</article-title> <source>Frontiers in Endocrinology</source> <year>2023</year> <month>01</month> <volume>13</volume> <object-id pub-id-type="doi" specific-use="metadata">10.3389/fendo.2022.1070074</object-id></element-citation></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
