Adrenocortical carcinoma presenting as a rupture and extensive retroperitoneal haemorrhage

Adrenocortical carcinoma (ACC) is an extremely rare tumour. We are reporting a 45-year-male patient who had a history of sudden severe worsening epigastric pain and fullness in abdomen, with giddiness. The radiological investigations showed a large right suprarenal mass with extensive destruction an...

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Published inJournal of clinical and diagnostic research Vol. 8; no. 3; pp. 117 - 118
Main Authors Jagtap, Sunil Vitthalrao, Desai, Sushama, Halder, Sandeepan, Jagtap, Swati S, Badwe, Anuya Shrikant
Format Journal Article
LanguageEnglish
Published India JCDR Research and Publications (P) Limited 01.03.2014
JCDR Research and Publications Private Limited
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Summary:Adrenocortical carcinoma (ACC) is an extremely rare tumour. We are reporting a 45-year-male patient who had a history of sudden severe worsening epigastric pain and fullness in abdomen, with giddiness. The radiological investigations showed a large right suprarenal mass with extensive destruction and retroperitoneal haemorrhage, with extra capsular, periportal and liver metastases. Exploratory laparotomy was done for excisions of mass and surrounding tissue. On histopathological examination, diagnosis was given as Adreno Cortical Carcinoma with capsular, vascular, and soft tissue nodular involvement.
ISSN:2249-782X
0973-709X
DOI:10.7860/JCDR/2014/6276.4128