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[IgD型多发性骨髓瘤。文献报道102例病例的综述(作者译)]

[IgD-multiple myeloma. Review of 102 cases reported in the literature (author's transl)].

作者信息

Knolle J, Meyer K H

出版信息

Immun Infekt. 1975 Jul;3(3):125-34.

PMID:810409
Abstract

Reports on 102 patients suffering from IgD-myeloma are reviewed and analyzed. Patients with IgD-myeloma are younger than patients with myeloma producing IgG or IgA myeloma proteins. Males are affected by this disease 3 times as often as females and 11 times as often as female patients in the group producing kappa light chain type of IgD myeloma protein. Hyperproteinaemia and extreme spikes of the monoclonal immunoglobulin occur less often. Approximately 90% of the patients have a lambda light chain myeloma protein and almost all patients excrete Bence-Jones protein. Renal insufficiency, amyloidosis, and plasma-cell leukemia are found more frequently than in other types of multiple myeloma. IgD-multiple myeloma carries a poorer prognosis, possibly related to the frequent finding of renal insufficiency.

摘要

对102例IgD型骨髓瘤患者的报告进行了回顾和分析。IgD型骨髓瘤患者比产生IgG或IgA骨髓瘤蛋白的骨髓瘤患者更年轻。男性受此病影响的频率是女性的3倍,在产生κ轻链型IgD骨髓瘤蛋白的组中是女性患者的11倍。高蛋白血症和单克隆免疫球蛋白的极端峰值较少见。约90%的患者有λ轻链骨髓瘤蛋白,几乎所有患者都排泄本周氏蛋白。与其他类型的多发性骨髓瘤相比,肾功能不全、淀粉样变性和浆细胞白血病更为常见。IgD多发性骨髓瘤的预后较差,可能与肾功能不全的频繁发现有关。

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