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Castleman's disease of the urachus.

机译:乌拉圭人的卡斯曼病。

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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.
机译:Castleman病(血管滤泡性淋巴增生)是原因不明的罕见的异种淋巴增生性疾病。尽管有胸外累及的报道,但多数病例以纵隔包块发生。涉及泌尿生殖道的Castleman病是受影响最罕见的器官系统之一,迄今为止仅在肾旁和腹膜后部位进行了描述。我们描述了一名患有单中心卡斯曼病的罕见病例,该病例位于尿道残余,并具有恶性外观。患者最初表现为腹痛,并接受腹腔镜根治性切除尿道肿块。病理检查显示为透明血管型Castleman病,伴有非典型淋巴样增生和滤泡性树突状细胞增生。未发现伴随淋巴瘤或肉瘤的迹象。手术切除肿瘤两年后,未见复发。据我们所知,这是卡斯曼氏病首例表现为尿道肿瘤。

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