Giant hemorrhagic myelolipoma in a patient with sickle cell disease

被引：6

作者：

Gamss C. ^{[1
,2
,3
]}

Chia F. ^{[2
]}

Chernyak V. ^{[2
]}

Rozenblit A. ^{[2
]}

机构：

[1] Albert Einstein College of Medicine, Yeshiva University, New York, NY

[2] Montefiore Medical Center, Bronx, NY 10467

[3] Radiology Department, Montefiore Medical Center, Bronx, NY 10467

来源：

Emergency Radiology | 2009年 / 16卷 / 4期

关键词：

Abdominal imaging; Adrenal mass; CT; Hemorrhage; MRI; Myelolipoma; Sickle cell disease;

D O I：

10.1007/s10140-008-0740-3

中图分类号：

学科分类号：

摘要：

Adrenal myelolipoma is a rare, benign tumor consisting of adipose tissue and hematopoetic elements. It is generally diagnosed as an incidental finding due to its nonfunctioning, asymptomatic nature (Meaglia and Schmidt J Urol 147:1089, 1992). With increasing size, however, as seen in this case, myelolipomas can cause flank pain and abdominal distention. This lesion was diagnosed in a young male with sickle cell disease during a vaso-occlusive crisis. © 2008 Am Soc Emergency Radiol.

引用

页码：319 / 322

页数：3

共 11 条

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