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表现为肾积水且与淋巴瘤难以鉴别的腹膜后Castleman病。

Retroperitoneal Castleman's disease presenting with hydronephrosis indistinguishable from lymphoma.

作者信息

Kim Young Sun, Jung Min Hyung

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Kyung Hee University Medical Center, Seoul, Korea.

出版信息

J Obstet Gynaecol Res. 2011 Aug;37(8):1145-8. doi: 10.1111/j.1447-0756.2010.01488.x. Epub 2011 Apr 19.

Abstract

Castleman's disease is a rare benign lymphoproliferative disease. We describe a patient with an unusual case of retroperitoneal Castleman's disease who initially presented with hydronephrosis. Her disease manifested with a malignant appearance in positron emission tomography/computed tomography and was located in the common and internal iliac area. Retrograde double-J stent insertion failed and nephrostomy was then performed. Complete surgical removal of the disease failed because the disease was severely adherent to the ureter and adjacent iliac vessels. Antegrade double-J stent insertion also failed. The patient eventually underwent laparoscopic ureteroneocystostomy. Retroperitoneal Castleman's disease should be added to the extensive list of differential diagnoses for primary retroperitoneal tumors.

摘要

卡斯特leman病是一种罕见的良性淋巴增生性疾病。我们描述了一例腹膜后卡斯特leman病的不寻常病例,该患者最初表现为肾积水。她的疾病在正电子发射断层扫描/计算机断层扫描中表现出恶性外观,位于髂总动脉和髂内动脉区域。逆行双J支架置入失败,随后进行了肾造瘘术。由于疾病与输尿管和相邻的髂血管严重粘连,完整手术切除失败。顺行双J支架置入也失败。患者最终接受了腹腔镜输尿管膀胱吻合术。腹膜后卡斯特leman病应添加到原发性腹膜后肿瘤的广泛鉴别诊断列表中。

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