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一名IgA和C4缺乏患者出现硬皮病和溶血性贫血:一种迄今未被描述的关联。

Scleroderma and hemolytic anemia in a patient with deficiency of IgA and C4: a hitherto undescribed association.

作者信息

Jones E, Jones J V, Woodbury J F, Carr R I, Skanes V

出版信息

J Rheumatol. 1987 Jun;14(3):609-12.

PMID:3625644
Abstract

We describe a 66-year-old women with CREST variant of scleroderma who developed autoimmune hemolytic anemia responsive to prednisone and demonstrated a deficiency of IgA and the C4 component of complement. This association of clinical, immunologic and genetic findings has not previously been reported. The literature relating to these findings is reviewed and possible mechanisms are discussed.

摘要

我们描述了一位66岁患有硬皮病CREST变异型的女性,她出现了对泼尼松有反应的自身免疫性溶血性贫血,并表现出IgA和补体C4成分缺乏。这种临床、免疫和遗传发现的关联此前尚未有报道。本文回顾了与这些发现相关的文献并讨论了可能的机制。

相似文献

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引用本文的文献

1
Infectious diseases associated with complement deficiencies.与补体缺陷相关的传染病。
Clin Microbiol Rev. 1991 Jul;4(3):359-95. doi: 10.1128/CMR.4.3.359.

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