CC BY-NC-ND 4.0 · World J Nucl Med 2022; 21(01): 073-075
DOI: 10.1055/s-0042-1746177
Case Report

Metastatic Pheochromocytoma Diagnosed with 131I-MIBG SPECT/CT Imaging in a Patient with Pathogenic VHL Mutation

Kousik Vankadari
1   Department of Nuclear Medicine, Yashoda Hospital, Secunderabad, Telangana, India
,
Raman Boddula
2   Department of Endocrinology, Yashoda Hospital, Secunderabad, Telangana, India
,
Aditya Gajanan Hegde
2   Department of Endocrinology, Yashoda Hospital, Secunderabad, Telangana, India
,
Chimutai Chinte
2   Department of Endocrinology, Yashoda Hospital, Secunderabad, Telangana, India
› Author Affiliations
Funding None.

Abstract

Pheochromocytoma is a rare catecholamine secreting neuroendocrine tumor arising from chromaffin cells of adrenal medulla with approximate prevalence of 0.1 to 0.6% in patients suffering from hypertension. Hypertensive control followed by surgical resection remains the primary treatment of choice. Although it is considered a slow growing benign tumor, it rarely leads to recurrence of tumor in the lymph nodes, liver, and lungs. Association of benign pheochromocytoma with familial or de novo Von Hippel-Lindau (VHL) mutations is well reported in literature. Here, we report a case of metastatic pheochromocytoma arising from commonly seen benign VHL mutation.

Consent

Appropriate patient consent isobtained for publishing the images and clinical information regarding the patient without revealing patient identity.




Publication History

Article published online:
30 April 2022

© 2022. World Association of Radiopharmaceutical and Molecular Therapy (WARMTH). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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