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与IgG型多发性骨髓瘤相关的补体Clq完全缺乏症。

Complete Clq deficiency associated with IgG multiple myeloma.

作者信息

Tokumitsu S, Furuta Y, Kobayashi T, Amano T, Suzuki S, Ota Z

机构信息

Department of Internal Medicine, Kawasaki Hospital, Kawasaki Medical School, Okayama, Japan.

出版信息

Jpn J Med. 1989 Mar-Apr;28(2):216-8. doi: 10.2169/internalmedicine1962.28.216.

Abstract

We report a case of IgG multiple myeloma with selective complete Clq deficiency. The patient was a 75-year-old Japanese woman who exhibited urticaria on the arm and an absence of serum hemolytic complement activity (CH50). Further studies revealed no vasculitis in the urticarial lesion but showed selective complete deficiency of Clq without low molecular weight Clq precipitin. Addition of highly purified Clq restored the CH50 level of the patient's serum to normal. It is suggested that this abnormality was a primary Clq deficiency. We discussed a relationship between the Clq deficiency and myeloma and reviewed the literature.

摘要

我们报告一例伴有选择性完全性C1q缺乏的IgG型多发性骨髓瘤病例。患者为一名75岁的日本女性,其手臂出现荨麻疹且血清溶血补体活性(CH50)缺失。进一步研究显示,荨麻疹皮损处无血管炎,但存在选择性完全性C1q缺乏,且无低分子量C1q沉淀素。添加高度纯化的C1q可使患者血清CH50水平恢复正常。提示这种异常为原发性C1q缺乏。我们讨论了C1q缺乏与骨髓瘤之间的关系并复习了相关文献。

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