Case Report

Large Adrenal Ganglioneuroma Presenting with Clinical Pheochromocytoma: A Rare Case Report

Abstract

Adrenal ganglioneuromas are rare benign and non-secretory neoplasms that, in the majority of cases, are unexpectedly discovered during imaging studies. In this study, we reported a large adrenal ganglioneuromas in a young patient, clinically presented as a pheochromocytoma. Laboratory evaluation and tumor markers were also report- ed in the normal range. The mass was then resected through laparoscopy. Ultimate- ly, histopathology revealed the diagnosis of Ganglioneuroma. Large adrenal gangli- oneuromas can be resected laparoscopically without any complications. An accurate pathological examination is usually essential for definitive diagnosis. Prognosis of ma- ture adrenal ganglioneuromas is excellent.

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IssueVol 7 No 4 (2022): July-August QRcode
SectionCase Report(s)
DOI https://doi.org/10.18502/crcp.v7i4.11590
Keywords
Ganglioneuroma Laparoscopic adrenalectomy Adrenal tumor

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How to Cite
1.
Farashi E, Rasihashemi SZ, Halimi M. Large Adrenal Ganglioneuroma Presenting with Clinical Pheochromocytoma: A Rare Case Report. CRCP. 2023;7(4):167-171.