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脐尿管的卡斯特曼病

Castleman's disease of the urachus.

作者信息

Rudloff Udo, Jacobson Avrum, Morgenstern Nora, Chen Yu, Lee Benjamin R

机构信息

Department of Surgery, North Shore University Hospital, Manhasset, New York, USA.

出版信息

Urology. 2004 Aug;64(2):376-9. doi: 10.1016/j.urology.2004.04.020.

Abstract

Castleman's disease (angiofollicular lymphoid hyperplasia) is a rare heterogeneous group of lymphoproliferative disorders of uncertain cause. Most cases occur as mediastinal masses, although extrathoracic involvement has been reported. Castleman's disease involving the genitourinary tract, one of the most infrequent organ systems affected, has so far only been described in pararenal and retroperitoneal locations. We describe a patient with an unusual case of unicentric Castleman's disease that was located in a urachal remnant and bore a malignant appearance. The patient initially presented with abdominal pain and underwent laparoscopic radical excision of the urachal mass. Pathologic examination revealed Castleman's disease, hyaline-vascular type, with atypical lymphoid proliferation and follicular dendritic cell dysplasia. No evidence of concomitant lymphoma or sarcoma was found. Two years after surgical removal of the tumor, no recurrence was evident. To our knowledge, this is the first case of Castleman's disease presenting as a urachal tumor.

摘要

卡斯特尔曼病(血管滤泡性淋巴组织增生)是一组病因不明的罕见异质性淋巴增殖性疾病。大多数病例表现为纵隔肿块,不过也有胸外受累的报道。卡斯特尔曼病累及泌尿生殖道,这是最不常受累的器官系统之一,迄今为止仅在肾旁和腹膜后部位有过描述。我们报告一例罕见的单中心卡斯特尔曼病,位于脐尿管残端,外观呈恶性。患者最初因腹痛就诊,接受了脐尿管肿块的腹腔镜根治性切除术。病理检查显示为透明血管型卡斯特尔曼病,伴有非典型淋巴样增生和滤泡树突状细胞发育异常。未发现合并淋巴瘤或肉瘤的证据。手术切除肿瘤两年后,未见复发迹象。据我们所知,这是首例表现为脐尿管肿瘤的卡斯特尔曼病。

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