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IgD型多发性骨髓瘤。133例病例回顾。

IgD multiple myeloma. Review of 133 cases.

作者信息

Jancelewicz Z, Takatsuki K, Sugai S, Pruzanski W

出版信息

Arch Intern Med. 1975 Jan;135(1):87-93.

PMID:1111472
Abstract

One hundred thirty-three patients had IgD myeloma. The IgD comprises 0.8% of M-components in general and 2.1% of myelomas in particular. Males predominate and 65% of the patients are younger than 60 years at the diagnosis. More than half of the patients have lymphadenopathy, hepatomegaly, or splenomegaly. Extraosseous spread and amyloidosis are frequent. Severe anemia and azotemia are common. Total serum protein and IgD M-component levels are usually not high. LAMBDA-type light chains are found in 90% of IgD M-components. Bence Jones proteinimia is frequent and Bence Jones proteinuria appears in almost all patients. Mean survival is 13.7 months from diagnosis. The IgD is different from IgG and IgA myeloma, indicating that the clinical picture and course of multiple cyeloma may be related to the class and type of M-component.

摘要

133例患者患有IgD型骨髓瘤。IgD一般占M蛋白成分的0.8%,在骨髓瘤中则占2.1%。男性居多,65%的患者在诊断时年龄小于60岁。超过半数的患者有淋巴结病、肝肿大或脾肿大。骨外扩散和淀粉样变性很常见。严重贫血和氮质血症也很普遍。血清总蛋白和IgD M蛋白成分水平通常不高。90%的IgD M蛋白成分中可发现λ型轻链。本-周蛋白血症很常见,几乎所有患者都会出现本-周蛋白尿。从诊断开始计算,平均生存期为13.7个月。IgD型骨髓瘤与IgG型和IgA型骨髓瘤不同,这表明多发性骨髓瘤的临床表现和病程可能与M蛋白成分的类别和类型有关。

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