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起源于肾包膜并由肾包膜动脉供血的肾脏孤立性纤维瘤。

Solitary fibrous tumor of the kidney originating from the renal capsule and fed by the renal capsular artery.

作者信息

Yamada Hiroshi, Tsuzuki Toyonori, Yokoi Keisuke, Kobayashi Hiroaki

机构信息

Department of Urology, Nagoya Daini Red Cross Hospital, 2-9 Myoken-cho Showa-ku, Nagoya 466-8650, Japan.

出版信息

Pathol Int. 2004 Dec;54(12):914-7. doi: 10.1111/j.1440-1827.2004.01772.x.

Abstract

Solitary fibrous tumors (SFT) are relatively rare spindle cell neoplasms that typically arise in the pleura. Recently, extrathoracic SFT that have arisen in various anatomic sites have been recognized. The histogenesis and prognosis of SFT of the kidney are not well understood because only 11 cases have been reported. We report a case of SFT of the left kidney arising from the renal capsule. The tumor was merged with the upper pole of the left renal capsule. The angiography revealed that the renal capsule artery fed the tumor. The tumor was a well-circumscribed, solid mass attached to the renal capsule without necrosis or hemorrhage. Microscopically the bland spindle cells proliferated and were accompanied by hyalinized collagenous tissue showing patternless or hemangiopericytomatous patterns. Some glomeluri and renal tubules were entrapped by the tumor cells. There were no mitotic figures. Immunohistochemically the tumor cells were diffusely positive for CD34, CD99 and bcl-2. There was no evidence of recurrence after a 4 year follow-up visit. The origin of SFT of the kidney remains uncertain. The tumor in this case merged with the renal capsule and was fed by the renal capsular artery, which suggests that some SFT of the kidney originate from the renal capsule.

摘要

孤立性纤维性肿瘤(SFT)是相对罕见的梭形细胞肿瘤,通常发生于胸膜。近来,已认识到发生于各种解剖部位的胸外SFT。肾SFT的组织发生和预后尚不清楚,因为仅报道了11例。我们报告1例起源于肾包膜的左肾SFT。肿瘤与左肾包膜上极融合。血管造影显示肾包膜动脉供血给肿瘤。肿瘤为边界清楚的实性肿块,附着于肾包膜,无坏死或出血。显微镜下,温和的梭形细胞增生,并伴有玻璃样变的胶原组织,呈无模式或血管外皮细胞瘤样模式。一些肾小球和肾小管被肿瘤细胞包绕。未见核分裂象。免疫组化显示肿瘤细胞CD34、CD99和bcl-2弥漫阳性。4年随访无复发证据。肾SFT的起源仍不确定。本例肿瘤与肾包膜融合,并由肾包膜动脉供血,提示部分肾SFT起源于肾包膜。

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