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

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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.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Metastatic Pheochromocytoma Diagnosed with 131I-MIBG SPECT/CT Imaging in a Patient with Pathogenic VHL Mutation ; volume:21 ; number:01 ; year:2022 ; pages:073-075
World Journal of Nuclear Medicine ; 21, Heft 01 (2022), 073-075

Beteiligte Personen und Organisationen
Vankadari, Kousik
Boddula, Raman
Hegde, Aditya Gajanan
Chinte, Chimutai

DOI
10.1055/s-0042-1746177
URN
urn:nbn:de:101:1-2022100815515678779792
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:25 MESZ

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Beteiligte

  • Vankadari, Kousik
  • Boddula, Raman
  • Hegde, Aditya Gajanan
  • Chinte, Chimutai

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