Late recurrent adrenocortical carcinoma presenting radiologically as a gastrointestinal stromal tumour: A case report
Author(s) -
Asmaa Beltagy,
Ahmed Kotb,
Mohamed Shaaban,
Mona AbdelHadi,
Ahmed Elabbady,
M.A. Atta,
M Hamza,
Mohamed Abdel-Rahman
Publication year - 2016
Publication title -
african journal of urology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.174
H-Index - 11
eISSN - 1110-5704
pISSN - 1961-9987
DOI - 10.1016/j.afju.2016.05.001
Subject(s) - adrenocortical carcinoma , medicine , gist , malignancy , adrenalectomy , metastasis , stromal tumor , distant metastasis , stromal cell , carcinoma , abdominal mass , incidence (geometry) , radiology , pathology , general surgery , surgery , cancer , physics , optics
Adrenocortical carcinoma (ACC) is a rare malignancy with an estimated incidence of 1–2 per million people. It may recur, after complete surgical removal by local or distant metastasis.ObservationWe report a case of late metastatic ACC presented as a mesenteric mass, 10 years post left adrenalectomy. Our case was initially misdiagnosed radiologically as gastrointestinal stromal tumour (GIST), and then the decision for exploration was made. The mass could be safely excised and confirmed pathologically to be an adrenocortical tumour
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