Miadonna A, Salmaso C, Palazzi P, Elli A, Braidotti P, Lambertenghi Deliliers G
Divisione di Medicina Interna, IRCCS Ospedale Maggiore Policlinico, Milano, Italy.
Leuk Lymphoma. 1998 Jan;28(3-4):429-35. doi: 10.3109/10428199809092700.
Castleman's disease is an uncommon lymph node disorder which can be associated with renal disease. In this report we describe a patient with fever, weight loss, anorexia, increase in inflammatory proteins, anemia and nephrotic syndrome. Castleman's disease, plasma cell type, was diagnosed by histologic analysis after surgical excision of a pelvic lymph node. The disease was considered localized, since further investigations did not show any other pathologic mass. After resection of the pelvic lymphoid mass, clinical remission of systemic symptoms and laboratory abnormalities was observed, with the exception of the nephrotic syndrome. Renal biopsy was performed and showed a pattern compatible with fibrillary glomerulonephritis. Progressive decline in renal function was observed, despite immunosuppressive therapy.
卡斯特曼病是一种罕见的淋巴结疾病,可与肾脏疾病相关。在本报告中,我们描述了一名伴有发热、体重减轻、厌食、炎症蛋白升高、贫血和肾病综合征的患者。通过对盆腔淋巴结进行手术切除后进行组织学分析,诊断为浆细胞型卡斯特曼病。由于进一步检查未发现任何其他病理性肿块,该疾病被认为是局限性的。切除盆腔淋巴肿块后,观察到全身症状和实验室异常出现临床缓解,但肾病综合征除外。进行了肾活检,结果显示符合纤维性肾小球肾炎的模式。尽管进行了免疫抑制治疗,但仍观察到肾功能逐渐下降。