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<article article-type="review-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/probl13651</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-13651</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>Clinical Case Series of Destructive Thyrotoxicosis Associated with Hashimoto’s Thyroiditis Misdiagnosed as Graves’ Disease: Clinical Patterns, Diagnostic Pitfalls, and Hypothesized Molecular Insights</article-title><trans-title-group xml:lang="en"><trans-title>Clinical Case Series of Destructive Thyrotoxicosis Associated with Hashimoto’s Thyroiditis Misdiagnosed as Graves’ Disease: Clinical Patterns, Diagnostic Pitfalls, and Hypothesized Molecular Insights</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5480-1688</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Akl</surname><given-names>Maher Monir.</given-names></name><name name-style="western" xml:lang="en"><surname>Akl</surname><given-names>Maher Monir.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Maher Monir Akl - Faculty of Medicine, National Research Lobachevsky State University of Nizhny Novgorod</p><p>Nizhny Novgorod</p></bio><bio xml:lang="en"><p>Maher Monir Akl - Faculty of Medicine, National Research Lobachevsky State University of Nizhny Novgorod</p><p>Nizhny Novgorod</p></bio><email xlink:type="simple">maherakl555@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/0000-0003-3477-236X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ahmed</surname><given-names>Amr</given-names></name><name name-style="western" xml:lang="en"><surname>Ahmed</surname><given-names>Amr</given-names></name></name-alternatives><bio xml:lang="ru"><p>Amr Ahmed - The public health department, Riyadh First Health Cluster, Ministry of Health</p></bio><bio xml:lang="en"><p>Amr Ahmed - The public health department, Riyadh First Health Cluster, Ministry of Health</p></bio><email xlink:type="simple">drmedahmed@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>National Research Lobachevsky State University of Nizhny Novgorod</institution><country>Египет</country></aff><aff xml:lang="en"><institution>National Research Lobachevsky State University of Nizhny Novgorod</institution><country>Egypt</country></aff></aff-alternatives><aff xml:lang="en" id="aff-2"><institution>The public health department, Riyadh First Health Cluster, Ministry of Health</institution><country>Saudi Arabia</country></aff><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>22</day><month>07</month><year>2026</year></pub-date><volume>72</volume><issue>3</issue><fpage>29</fpage><lpage>35</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Akl M., Ahmed A., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Akl M., Ahmed A.</copyright-holder><copyright-holder xml:lang="en">Akl M., Ahmed A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" 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/13651">https://www.probl-endojournals.ru/jour/article/view/13651</self-uri><abstract><p>This descriptive clinical case series analyzes five cases of destructive thyrotoxicosis associated with Hashimoto’s thyroiditis, historically referred to as hashitoxicosis, initially misdiagnosed as Graves’ disease, highlighting a persistent diagnostic challenge in autoimmune thyroid disorders. The series includes four published cases reported between 2000 and 2025 and one unpublished case contributed by the authors. The cohort comprised three females and two males, with a mean age of 55.4 years (range: 21–69). Clinical presentations were heterogeneous, most commonly fatigue (80%), palpitations (60%), and weight changes (40%), while two patients exhibited no overt hyperthyroid symptoms.</p><p>Biochemical evaluation demonstrated suppressed thyroid-stimulating hormone (TSH) levels in all cases (range: &lt;0.000–0.13 µIU/mL), elevated anti-thyroid peroxidase (anti-TPO) antibodies in 80% (range: 41–&gt;1,000 IU/mL), and initially negative thyroid-stimulating hormone receptor antibodies (TRAb/TSI) in 60% of patients. Seroconversion to positive TRAb/TSI was observed in two cases during follow-up, suggesting autoimmune overlap rather than definitive disease transition. Imaging findings, including thyroid ultrasonography and radioiodine uptake (RAI) studies, consistently favored destructive thyroiditis over stimulatory hyperthyroidism, with heterogeneous echotexture observed in 75% of assessed cases and low or normal RAI uptake in all evaluated patients.</p><p>Misdiagnosis occurred in 80% of cases, predominantly due to reliance on suppressed TSH levels without TRAb confirmation, resulting in inappropriate antithyroid drug administration in 80% and accelerated hypothyroidism in 60%. Immunopathological interpretation based on existing literature supports a predominantly Th1-mediated destructive process, in contrast to the Th2-driven antibody-mediated stimulation characteristic of Graves’ disease, with rare Th1-to-Th2 immune shifts reported. Clinical outcomes ranged from spontaneous resolution to surgical intervention.</p><p>This case series underscores the importance of mandatory TRAb testing, adherence to American and European Thyroid Association guidelines, and early specialist referral to reduce iatrogenic harm and improve diagnostic precision in autoimmune thyroid disease.</p></abstract><trans-abstract xml:lang="en"><p>This descriptive clinical case series analyzes five cases of destructive thyrotoxicosis associated with Hashimoto’s thyroiditis, historically referred to as hashitoxicosis, initially misdiagnosed as Graves’ disease, highlighting a persistent diagnostic challenge in autoimmune thyroid disorders. The series includes four published cases reported between 2000 and 2025 and one unpublished case contributed by the authors. The cohort comprised three females and two males, with a mean age of 55.4 years (range: 21–69). Clinical presentations were heterogeneous, most commonly fatigue (80%), palpitations (60%), and weight changes (40%), while two patients exhibited no overt hyperthyroid symptoms.</p><p>Biochemical evaluation demonstrated suppressed thyroid-stimulating hormone (TSH) levels in all cases (range: &lt;0.000–0.13 µIU/mL), elevated anti-thyroid peroxidase (anti-TPO) antibodies in 80% (range: 41–&gt;1,000 IU/mL), and initially negative thyroid-stimulating hormone receptor antibodies (TRAb/TSI) in 60% of patients. Seroconversion to positive TRAb/TSI was observed in two cases during follow-up, suggesting autoimmune overlap rather than definitive disease transition. Imaging findings, including thyroid ultrasonography and radioiodine uptake (RAI) studies, consistently favored destructive thyroiditis over stimulatory hyperthyroidism, with heterogeneous echotexture observed in 75% of assessed cases and low or normal RAI uptake in all evaluated patients.</p><p>Misdiagnosis occurred in 80% of cases, predominantly due to reliance on suppressed TSH levels without TRAb confirmation, resulting in inappropriate antithyroid drug administration in 80% and accelerated hypothyroidism in 60%. Immunopathological interpretation based on existing literature supports a predominantly Th1-mediated destructive process, in contrast to the Th2-driven antibody-mediated stimulation characteristic of Graves’ disease, with rare Th1-to-Th2 immune shifts reported. Clinical outcomes ranged from spontaneous resolution to surgical intervention.</p><p>This case series underscores the importance of mandatory TRAb testing, adherence to American and European Thyroid Association guidelines, and early specialist referral to reduce iatrogenic harm and improve diagnostic precision in autoimmune thyroid disease.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Thyrotoxicosis Associated with Hashimoto’s Thyroiditis</kwd><kwd>Graves’ disease</kwd><kwd>Misdiagnosis</kwd><kwd>Autoimmune thyroid disorders</kwd><kwd>Molecular pathways</kwd><kwd>TRAb testing</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Thyrotoxicosis Associated with Hashimoto’s Thyroiditis</kwd><kwd>Graves’ disease</kwd><kwd>Misdiagnosis</kwd><kwd>Autoimmune thyroid disorders</kwd><kwd>Molecular pathways</kwd><kwd>TRAb testing</kwd></kwd-group><funding-group><funding-statement xml:lang="en">the authors received no financial support for the research, authorship, and/or publication of this article</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Shahbaz, A., Aziz, K., Umair, M., &amp; Sachmechi, I. 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