Sanders R, Bissada N, Curry N, Gordon B
Medical University of South Carolina, Charleston 29425, USA.
J Urol. 1995 Jun;153(6):1791-3.
Adrenal myelolipoma is a rare, benign, and biochemically nonfunctioning tumor. Most patients with adrenal myelolipoma are asymptomatic and the condition is discovered incidentally at autopsy. Review of the literature reveals 70 patients with surgically documented adrenal myelolipoma. We report 7 additional patients with 8 adrenal myelolipomas, of whom 5 underwent surgical removal because of tumor size, unusual imaging features or symptomatology. Of our patients 4 had symptomatic lesions requiring surgical removal, while 1 had an adrenal myelolipoma that was discovered intraoperatively. Of the remaining 2 patients 1 had a small (3 cm.) lesion discovered incidentally on excretory urography and 1 had bilateral adrenal myelolipoma discovered incidentally on computerized tomography.
肾上腺髓质脂肪瘤是一种罕见的良性、无生化功能的肿瘤。大多数肾上腺髓质脂肪瘤患者无症状,常在尸检时偶然发现。文献回顾显示有70例经手术证实的肾上腺髓质脂肪瘤患者。我们报告另外7例患者共8个肾上腺髓质脂肪瘤,其中5例因肿瘤大小、不寻常的影像学特征或症状而接受手术切除。我们的患者中,4例有需要手术切除的有症状病变,1例肾上腺髓质脂肪瘤是在术中发现的。其余2例患者中,1例在排泄性尿路造影时偶然发现一个小(3厘米)病变,1例在计算机断层扫描时偶然发现双侧肾上腺髓质脂肪瘤。