Cabrera Fernando, Villacampa Felipe, Duque Gemma, Leiva Oscar
Service of Urology, Hospital Universitario 12 Octubre, Madrid, Spain.
Arch Esp Urol. 2013 May;66(4):377-9.
We report one case of Castleman's disease and review published literature.
We report the case of a 58 year old man who was referred to our institution because of lumbar pain. A computed tomography scan revealed a retroperitoneal mass. Open surgical exploration and excision were carried out. Finally pathological examination addressed the diagnosis.
Pathological examination demonstrated findings characteristic of unicentric hyaline vascular type of Castleman's disease. After surgical excision and 12 months follow-up there is no evidence of recurrence disease.
Castleman's disease is a rare lymphoproliferative disorder of uncertain etiology. Retroperitoneal localization is exceptional.
我们报告一例Castleman病病例并回顾已发表的文献。
我们报告一名58岁男性因腰痛转诊至我院的病例。计算机断层扫描显示腹膜后肿块。进行了开放手术探查和切除。最后通过病理检查明确诊断。
病理检查显示为单中心透明血管型Castleman病的特征性表现。手术切除后随访12个月，无疾病复发迹象。
Castleman病是一种病因不明的罕见淋巴增生性疾病。腹膜后定位较为罕见。
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