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伴有溶骨性骨病变及浆细胞形态的华氏巨球蛋白血症。病例报告。

Waldenstroöm's macroglobulinemia with lytic osseous lesions and plasma-cell morphology. Report of a case.

作者信息

Berman H H

出版信息

Am J Clin Pathol. 1975 Mar;63(3):397-402. doi: 10.1093/ajcp/63.3.397.

Abstract

A 44-year-old man had Waldenström's macroglobulinemia, diagnosed on the basis of serum protein studies. A predominantly plasmacytic bone-marrow morphology and significant osseous lesions were present. This case and others in the literature indicate that osseous lesions are not uncommon in Waldenstöm's macroglobulinemia, that occasional patients with this disease have proliferation mainly of plasma cells, and that a plasma-cell morphology is usually associated with the development of osteolytic lesions. Waldenström's macroglobulinemia and multiple myeloma may merely be opposite ends of the same disease spectrum, with intermediate forms, such as the case in point, occurring.

摘要

一名44岁男性患有华氏巨球蛋白血症,该诊断基于血清蛋白研究得出。其骨髓形态以浆细胞为主,并存在明显的骨质病变。该病例及文献中的其他病例表明,骨质病变在华氏巨球蛋白血症中并不罕见,该疾病的部分患者主要表现为浆细胞增殖,且浆细胞形态通常与溶骨性病变的发生有关。华氏巨球蛋白血症和多发性骨髓瘤可能只是同一疾病谱的两端,会出现如本例这样的中间形式。

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