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伴有骨髓纤维化和淀粉样变性的IgD骨髓瘤

IgD myeloma with myelofibrosis and amyloidosis.

作者信息

Udoji W C, Pemmaraju S

出版信息

Arch Pathol Lab Med. 1977 Jan;101(1):10-3.

PMID:401635
Abstract

Two patients with IgD myeloma protein and lambda light chains are described. They had marked Bence Jones proteinuria, were treated with melphalan, prednisone, and allopurinol and died in less than one year. At autopsy, there was extensive myelofibrosis associated with neoplastic infiltrates of plasma cells in both cases. On electrophoresis, the serum and urine Bence Jones protein of one patient migrated in the alpha2 region, and the blood vessels of the other patient contained many nodular deposits of amyloid. Because these findings are rare in multiple myeloma, they may be unique to IgD myeloma.

摘要

本文描述了两名患有IgD骨髓瘤蛋白和λ轻链的患者。他们有明显的本-周蛋白尿,接受了美法仑、泼尼松和别嘌醇治疗,不到一年便去世。尸检时,两例均发现广泛的骨髓纤维化,并伴有浆细胞瘤浸润。电泳显示,其中一名患者的血清和尿本-周蛋白在α2区迁移,另一名患者的血管中有许多淀粉样结节沉积。由于这些发现在多发性骨髓瘤中很少见,可能是IgD骨髓瘤所特有的。

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