Carrion Diego M, Alvarez-Maestro Mario, Gómez Rivas Juan, Brygadyr Yaroslav, García-Fernandez Eugenia, Martínez-Piñeiro Luis
Department of Urology, La Paz University Hospital, Madrid, Spain,
Department of Urology, La Paz University Hospital, Madrid, Spain.
Urol Int. 2019;103(2):245-248. doi: 10.1159/000493511. Epub 2018 Oct 10.
Castleman's disease (CD) is an uncommon type of lymphoproliferative disorder. Its etiology and prevalence are unclear. The retroperitoneum is a very rare site for presentation of the unicentric variant, where it mimics malignant tumors. A 59-year-old man is referred to the urology outpatient clinic for the study of microhematuria found in a routine analysis. CT scan of the abdomen identified a solid, circumscribed mass, measuring 28 × 30 × 31 mm in the left para-aortic zone, with homogeneous contrast enhancement. Excisional surgery and regional lymphadenectomy were performed via laparoscopy. Postoperative course concurred without incidences. Histological diagnosis confirmed unicentric CD, hyaline-vascular type. CD is a rare entity, and the unicentric type presents as an asymptomatic mass. Retroperitoneum is a rare localization, where initial imaging diagnosis is unclear and surgical resection is the preferred treatment.
卡斯特曼病(CD)是一种罕见的淋巴增生性疾病。其病因和患病率尚不清楚。腹膜后是单中心型卡斯特曼病非常罕见的发病部位,在此处它会模仿恶性肿瘤。一名59岁男性因在常规分析中发现微血尿而被转诊至泌尿外科门诊。腹部CT扫描发现左主动脉旁区有一个实性、边界清晰的肿块,大小为28×30×31mm,对比增强均匀。通过腹腔镜进行了切除手术和区域淋巴结清扫术。术后过程顺利,无并发症。组织学诊断证实为单中心型卡斯特曼病,透明血管型。卡斯特曼病是一种罕见的疾病,单中心型表现为无症状肿块。腹膜后是罕见的发病部位,初始影像学诊断不明确,手术切除是首选治疗方法。