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5例肾窦血管平滑肌脂肪瘤的MRI表现

MRI findings of angiomyolipoma of the renal sinus in 5 cases.

作者信息

Kamath Amita, Rosenkrantz Andrew B, Bosniak Morton A

机构信息

Department of Radiology, NYU Langone Medical Center, New York, NY 10016, USA.

出版信息

J Comput Assist Tomogr. 2010 Nov-Dec;34(6):915-20. doi: 10.1097/RCT.0b013e3181ebe8ea.

Abstract

The magnetic resonance imaging (MRI) appearance of 5 cases of angiomyolipoma (AML) centered in the renal sinus is presented. All cases exhibited similar imaging findings, including well-circumscribed margins, minimal perceived enhancement without soft tissue components, insinuation around the renal collecting system, and localized hydrocalicosis with associated localized renal parenchymal atrophy but without generalized hydronephrosis. Findings in some cases included extension out of the renal sinus and presence of aneurysmal vessels. Although identification of a renal parenchymal defect has been reported to be useful for the differentiation of a large exophytic AML from a perirenal liposarcoma, none of the cases in our series demonstrated this finding on MRI. To our knowledge, there have been only 2 previous reported cases showing the cross-sectional imaging appearance of an AML of the renal sinus without a renal parenchymal defect. In view of the shared and characteristic imaging features of the 5 cases in our series, we believe that the diagnosis of this condition can be strongly suggested by MRI despite the absence of a visible parenchymal defect. While histology remains the only way to definitively establish the diagnosis, the typical imaging appearance of this entity should enable conservative management with follow-up imaging in an asymptomatic patient. In some cases, embolization and needle biopsy could be used to avoid a surgical approach.

摘要

本文介绍了5例以肾窦为中心的血管平滑肌脂肪瘤(AML)的磁共振成像(MRI)表现。所有病例均表现出相似的影像学特征,包括边界清晰、无软组织成分的轻微强化、沿肾集合系统蔓延、伴有局部肾实质萎缩的局限性肾盂积水但无普遍性肾积水。部分病例的表现包括延伸至肾窦外和存在动脉瘤样血管。虽然据报道,识别肾实质缺损有助于将巨大外生性AML与肾周脂肪肉瘤区分开来,但我们系列中的病例在MRI上均未显示这一表现。据我们所知,之前仅有2例报道显示肾窦AML的横断面成像表现而无肾实质缺损。鉴于我们系列中5例病例具有共同的特征性影像学表现,我们认为,尽管没有可见的实质缺损,MRI仍可强烈提示该病的诊断。虽然组织学仍然是明确诊断的唯一方法,但该实体典型的影像学表现应能使无症状患者通过随访成像进行保守治疗。在某些情况下,可采用栓塞和针吸活检以避免手术治疗。

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