KLI

A Case of Incidentally Detected Silent Adrenal Pheochromocytoma, Mimicking as an Intraperitoneal Tumor With Unusual Computed Tomography Findings

Metadata Downloads
Abstract
Pheochromocytoma is a rare functional adrenal tumor often producing catecholamines. Such secretion may induce hypertension, tachycardia or cardiac related symptoms. However, pheochromocytoma can present as an asymptomatic adrenal incidentaloma which may be difficult to detect; thus, leading to delay in proper surgical treatment. We report a 39-year-old female patient who presented with gastric gastrointestinal stromal tumor-like appearance on computed tomography, which was identified as a left retroperitoneal adrenal tumor after initial surgery. Before the second surgery, adrenal tumor shrinkage was detected without any causable event. The final pathology was confirmed as pheochromocytoma after the second surgery.
Issued Date
2023
Tae-Yon Sung
Type
Article
Keyword
Silent pheochromocytomaPheochromocytomaRetroperitoneal posterior adrenalectomy
DOI
10.16956/jes.2023.23.3.80
URI
https://oak.ulsan.ac.kr/handle/2021.oak/16212
Publisher
The Journal of Endocrine Surgery
Language
한국어
ISSN
2508-8149
Citation Volume
23
Citation Number
3
Citation Start Page
80
Citation End Page
84
Appears in Collections:
Medicine > Nursing
공개 및 라이선스
  • 공개 구분공개
파일 목록
  • 관련 파일이 존재하지 않습니다.

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.