Features of Asymptomatic Pheochromocytoma/Paraganglioma Based on Clinical-Laboratory Examination and Computed Tomography
https://doi.org/10.14341/probl13639
Abstract
BACKGROUND: Although pheochromocytomas and paragangliomas (PPGLs) classically present with distinct clinical signs, there is a category of patients with asymptomatic disease course. Despite the absence of clinical manifestations, these patients retain the risk of life-threatening hypertensive crisis and other cardiovascular complications. The clinical, laboratory, and imaging characteristics of asymptomatic PPGLs remain insufficiently studied and are of significant scientific and practical interest.
AIM: To analyze the clinical, laboratory, and imaging characteristics of asymptomatic PPGLs compared to symptomatic ones.
MATERIALS AND METHODS: The analysis included 347 patients with histologically confirmed PPGL who underwent surgery at the Saint Petersburg State University Hospital. Retrospective analysis encompassed demographic data, medical history (primary and comorbid conditions), laboratory findings, and computed tomography (CT) data. RESULTS: The PPGLs patient cohort included 45 cases without clinical signs of catecholamine hypersecretion. The asymptomatic subgroup, compared to symptomatic patients, exhibited younger age (43 [33; 51] vs. 48 [37; 57] years); smaller maximum tumor size (34 [27; 53] vs. 45 [34; 60] mm); lower metanephrine/normetanephrine ratio (0.29 [0.10; 0.79] vs. 0.51 [0.09; 1.23]).
CT imaging revealed slightly higher radiodensity values in asymptomatic PPGLs during arterial, venous, and delayed phases compared to symptomatic tumors. However, absolute and relative washout percentages did not differ significantly.
CONCLUSION: The younger age and smaller tumor size in asymptomatic PPGL patients suggest earlier detection of the disease compared to symptomatic cases. The lower metanephrine/normetanephrine ratio may indicate a higher prevalence of the norepinephrine-secreting phenotype in asymptomatic PPGLs. No pronounced differences were found in imaging characteristics between asymptomatic and symptomatic tumors.
About the Authors
D. V. RebrovaRussian Federation
Dina V. Rebrova, MD, PhD
154 Fontanka river embankment, 190103, Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
S. N. Fogt
Russian Federation
Sergei N. Fogt, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
R. A. Chernikov
Russian Federation
Roman A. Chernikov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
I. V. Sleptsov
Russian Federation
Ilya V. Sleptsov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
E. A. Fedorov
Russian Federation
Elisey A. Fedorov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
I. K. Chinchuk
Russian Federation
Igor K. Chinchuk, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
Sh. Sh. Shikhmagomedov
Russian Federation
Shamil S. Shikhmagomedov, MD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
N. V. Vorokhobina
Russian Federation
Natalya V. Vorokhobina, MD, PhD, Prof.
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
E. A. Zgoda
Russian Federation
Ekaterina A. Zgoda, MD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
A. A. Semenov
Russian Federation
Arseny A. Semenov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
V. F. Rusakov
Russian Federation
Vladimir F. Rusakov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
L. M. Krasnov
Russian Federation
Leonid M. Krasnov, MD, PhD
Saint Petersburg
Competing Interests:
Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с содержанием настоящей статьи.
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Supplementary files
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1. Figure 1. Maximum and working systolic and diastolic blood pressure in patients with pheochromocytoma/paraganglioma. | |
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2. Figure 2. Native radiographic tumor density and its dynamics after contrast administration in patients with pheochromocytoma/paraganglioma. | |
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3. Figure 3. Pheochromocytoma of the right adrenal gland, measuring 26 x 20 x 26 mm, predominantly metanephrine secretion, asymptomatic. Contrast-enhanced CT scan: a — native phase, density 20 HU; b — arterial phase, density up to 105 HU; c — venous phase, density up to 145 HU; d — delayed phase, density 50 HU. | |
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4. Figure 4. Pheochromocytoma of the right adrenal gland, dimensions 45 x 38 x 32 mm, normetanephrine secretion type, asymptomatic. Contrast-enhanced CT scan: a — native phase, density up to 35 HU; b — arterial phase, density up to 106 HU; c — venous phase, density up to 130 HU; d — delayed phase, density up to 82 HU. | |
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5. Figure 5. A pheochromocytoma of the left adrenal gland, measuring 11 x 10 x 11 mm, with a heterogeneous structure, clinically and biochemically "silent." Contrast-enhanced CT scan: a — native phase, density from 34 to 43 HU; b — arterial phase, density from 158 to 209 HU; c — venous phase, density from 111 to 139 HU; d — delayed phase, density up to 70 HU. | |
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Review
For citations:
Rebrova D.V., Fogt S.N., Chernikov R.A., Sleptsov I.V., Fedorov E.A., Chinchuk I.K., Shikhmagomedov Sh.Sh., Vorokhobina N.V., Zgoda E.A., Semenov A.A., Rusakov V.F., Krasnov L.M. Features of Asymptomatic Pheochromocytoma/Paraganglioma Based on Clinical-Laboratory Examination and Computed Tomography. Problems of Endocrinology. 2026;72(4):18-27. (In Russ.) https://doi.org/10.14341/probl13639
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