类风湿关节炎患者出现的血管免疫母细胞性淋巴结病伴蛋白血症。
Angioimmunoblastic lymphadenopathy with disproteinemia arising in a patient with rheumatoid arthritis.
作者信息
Ozoran K, Turgay M, Kinikli G, Duman M, Tolunay O, Tokgöz G
机构信息
Ankara University, Faculty of Medicine, Department of Immunology and Rheumatology, Turkey.
出版信息
Scand J Rheumatol. 1995;24(1):58-60. doi: 10.3109/03009749509095159.
PMID:7863284
Abstract
Angioimmunoblastic lymphadenopathy with disproteinemia (AILD) is a systemic lymphoproliferative disorder characterized by constitutional symptoms such as generalized lymphadenopathy, hepatosplenomegaly and skin rash. In this article, we report on a patient with seronegative Rheumatoid Arthritis of 18 years duration who recently developed AILD.
摘要
血管免疫母细胞性淋巴结病伴蛋白异常血症（AILD）是一种全身性淋巴增殖性疾病，其特征为全身性淋巴结肿大、肝脾肿大和皮疹等全身症状。在本文中，我们报告了一名患有18年血清阴性类风湿关节炎的患者，该患者最近患上了AILD。
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