特发性多中心Castleman病

S. Rupasinghe, W. Kularatne, T. Arikaran
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引用次数: 2

摘要

Castleman病是一种淋巴增生性疾病,具有典型的淋巴结组织病理学特征。根据受累淋巴结区域的数量,可分为单中心性和多中心性两种亚型。我们在此报告一位老年男性病患,表现为双侧下肢肿胀、全身淋巴结肿大及肝脏肿大。左侧颈淋巴结活检符合Castleman病的浆细胞型。他被诊断为患有特发性多中心Castleman病。他立即接受化疗和类固醇治疗,导致症状改善。准确的组织学诊断是重要的,因为CD在临床上可以模拟淋巴瘤,但预后不同。为了降低发病率和死亡率,早期诊断和治疗是必须的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic Multicentric Castleman Disease
Castleman disease [CD] is a lymphoproliferative disease which has characteristic lymph node histopathology. It is classified into two subtypes as unicentric CD and multicentric CD depending on the number of lymph node regions involved. Here we report a case of an elderly malepresenting with bilateral lower limb swelling, generalized lymphadenopathy and hepatomegaly. Left side cervical lymph node biospy was consistent with plasma cell type of Castleman disease. He was diagnosed as having‘not otherwise specified’ idiopathic multicentric Castleman disease. He was promptly treated with chemotherapy and steroids which led to improvement of symptoms. Accurate histological diagnosis is important since CD can clinically mimic lymphoma, which has a different prognosis. Early diagnosis and treatment is mandatory in order to reduce morbidity and mortality.
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