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[血管免疫母细胞性淋巴结病伴蛋白异常血症]

[Angioimmunoblastic lymphadenopathy with dysproteinemia].

作者信息

Marchi L, Frascisco M, Mairano D, Biarese V, Andrione P, Manachino D, Lovisetto P

出版信息

Recenti Prog Med. 1989 Jun;80(6):326-32.

PMID:2672196
Abstract

Angioimmunoblastic lymphadenopathy with dysproteinemia. Angioimmunoblastic lymphadenopathy with dysproteinemia is a lymphomatous-like disease associated with typical anatomopathological features of the lymph nodes and severe dysproteinemia. The clinical course is variable. Acquired immunodeficiency, oral infections, neoplastic development are frequently present. The evolution of the disease is also variable; spontaneous resolution as well as lethal complications are possible. No specific therapy is available. There are conflicting opinions about the nosographic statement of angioimmunoblastic lymphadenopathy among benign lymphadenopathy and lymphomas.

摘要

血管免疫母细胞性淋巴结病伴蛋白异常血症。血管免疫母细胞性淋巴结病伴蛋白异常血症是一种淋巴瘤样疾病,与淋巴结典型的解剖病理学特征及严重的蛋白异常血症相关。临床病程多变。常伴有获得性免疫缺陷、口腔感染及肿瘤发生。疾病的进展也不尽相同,可能自发缓解,也可能出现致命并发症。目前尚无特效治疗方法。对于血管免疫母细胞性淋巴结病在良性淋巴结病和淋巴瘤中的疾病分类归属存在不同观点。

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