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Adrenal Angiomyolipoma: A Case Report and Review of Literature

机译:肾上腺血管平滑肌脂肪瘤:一例报道并文献复习

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Angiomyolipoma of adrenal is extremely rare with few cases reported in literature. It usually presents as incidentiloma. We report a case of a 42 years old male patient presenting with pain abdomen, nausea and vomiting. USG abdomen showed features of acute calculus cholecystitis with right adrenal tumour. CECT abdomen revealed heterogenous non enhancing hypodense fatty lesion in right adrenal gland. Biochemical investigations were negative for functioning adrenal tumour. After conservative management of acute cholecystitis, interval cholecystectomy with resection of adrenal tumour was done. Histopathological examination of adrenal tumour showed features of adrenal angiomyolipoma.
机译:肾上腺血管肌脂瘤极少见,文献报道很少。它通常表现为偶发瘤。我们报告了一例42岁的男性患者,腹部疼痛,恶心和呕吐。 USG腹部表现为具有右肾上腺肿瘤的急性结石性胆囊炎。 CECT腹部显示右肾上腺异质性非增强性低密度脂肪病灶。生化检查对肾上腺肿瘤功能正常。保守治疗急性胆囊炎后,进行间隔性胆囊切除术并切除肾上腺肿瘤。肾上腺肿瘤的组织病理学检查显示出肾上腺血管平滑肌脂肪瘤的特征。

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