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血管免疫母细胞性淋巴结病伴蛋白异常血症:首例儿童病例报告,病情自然缓解

Angioimmunoblastic lymphadenopathy with dysproteinemia: report of the first case in childhood evolving toward spontaneous remission.

作者信息

Fiorillo A, Pettinato G, Raia V, Migliorati R, Angrisani P, Buffolano W

出版信息

Cancer. 1981 Oct 1;48(7):1611-4. doi: 10.1002/1097-0142(19811001)48:7<1611::aid-cncr2820480723>3.0.co;2-x.

Abstract

This is the first known report of a case of angioimmunoblastic lymphadenopathy, with dysproteinemia (AILD) in childhood which evolved toward a spontaneous remission. The disease had an acute onset with generalized lymphadenopathy, hepatosplenomegaly, high-grade fever and polyclonal hypergammaglobulinemia. The lymph nodes met all of the histologic criteria required for diagnosis as established by Frizzera et al. It is emphasized that AILD should be taken into consideration in the differential diagnosis of lymphadenopathy in childhood.

摘要

这是已知的首例儿童血管免疫母细胞性淋巴结病伴蛋白异常血症(AILD)自发缓解的病例报告。该疾病急性起病,有全身淋巴结肿大、肝脾肿大、高热及多克隆高丙种球蛋白血症。淋巴结符合Frizzera等人确立的诊断所需的所有组织学标准。需要强调的是,在儿童淋巴结病的鉴别诊断中应考虑到AILD。

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