Kim Young Sun, Jung Min Hyung
Department of Obstetrics and Gynecology, School of Medicine, Kyung Hee University Medical Center, Seoul, Korea.
J Obstet Gynaecol Res. 2011 Aug;37(8):1145-8. doi: 10.1111/j.1447-0756.2010.01488.x. Epub 2011 Apr 19.
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.
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。