Adrenal angiomyolipoma: A case report and review of literature

被引：6
|
作者：
Goswami, Amit [1 ]
Sharma, Anil [1 ]
Khullar, Rajesh [1 ]
Soni, Vandana [1 ]
Baijal, Manish [1 ]
Chowbey, Pradeep [1 ]
机构：
[1] Max Super Specialty Hosp, Dept Minimal Access Metab & Bariatr Surg, New Delhi, India
来源：
JOURNAL OF MINIMAL ACCESS SURGERY | 2014年 / 10卷 / 04期
关键词：
Adrenal; angiomyolipoma; laparoscopy; LAPAROSCOPIC ADRENALECTOMY;
D O I：
10.4103/0972-9941.141531
中图分类号：
R61 [外科手术学];
学科分类号：
摘要：
Angiomyolipoma (AML) is a rare mesenchymal tumour arising from perivascular epithelioid cells. It is most commonly seen in kidney, but rarely AML can arise in extra renal sites. Adrenal AML is a very rare clinical entity, and very few cases have been reported so far. We present our experience with a 43-year-old female, who presented with right flank pain. Magnetic resonance imaging showed a right adrenal mass. Laparoscopic adrenelectomy was performed, and the histopathology report confirmed the diagnosis of AML. Patient was discharged uneventfully.
引用
收藏
页码：213 / 215
页数：3
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