结节性硬化症患者的巨血管平滑肌脂肪瘤伴Wunderlich综合征

A. Tyagi, C. Reddy, N. Kumar, A. Reddy, A. Ganesh, K. Radhika
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引用次数: 0

摘要

25岁男性,右腰疼痛持续两周。检查时,他有面部皮脂腺瘤(图1),大体苍白,右腰椎严重压痛,右腰部肿块延伸至疑病症和髂区。腹部增强计算机断层扫描(CT)显示右侧肾脏增大,伴大量右肾包膜下血肿(图2),双侧肾实质内多中心结节,脂肪密度< 20 Hounsfield单位,提示双侧肾血管平滑肌脂肪瘤。脑CT显示室管膜下结节(图3)。脑室管膜结节合并皮脂腺瘤可诊断结节性硬化症。患者被复苏并计划进行右侧肾动脉栓塞,但由于血肿移位导致肾门解剖结构改变,手术失败。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant angiomyolipoma with Wunderlich’s syndrome in a patient with tuberous sclerosis
A 25-year-old male presented with right loin pain of two weeks duration. On examination, he had adenoma sebaceum over face (Figure 1), gross pallor, severe tenderness in right lumbar region and a right loin lump extending into hypochondriac and iliac regions. Contrast enhanced computed tomography (CT) of the abdomen revealed right side enlarged kidney with massive subcapsular right renal haematoma (Figure 2) and multicentric nodules with of fat densities (< 20 Hounsfield units) within both the renal parenchyma, suggestive of bilateral renal angiomyolipomas. CT of the brain showed subependymal nodules (Figure 3). This pattern of cerebral ependymal nodules together with adenoma sebaceum was diagnostic of tuberous sclerosis. Patient was resuscitated and planned right sided renal artery embolization but the procedure failed due to altered renal hilar anatomy due to displacement by haematoma.
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