难治性贫血患者的系统性红斑狼疮。

S Nakayama, F Nakamura, H Yabe, K Nagai
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引用次数: 0

摘要

一位69岁的男性被诊断为难治性贫血(RA),伴有持续两年的全血细胞减少症,所有三种细胞系骨髓增生异常,骨髓细胞核型异常46、XY、20q-,抗核和DNA抗体试验阳性。第一次就诊一年后,他出现了关节炎和黄斑丘疹。皮肤病变的组织学特征与盘状红斑狼疮相似。他被诊断为系统性红斑狼疮并发难治性贫血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic lupus erythematosus in a patient with refractory anemia.

A 69-year-old man was diagnosed as having refractory anemia (RA), accompanied by pancytopenia of two years' duration, myelodysplasia in all three cell lines, abnormal karyotype of 46, XY, 20q--in bone marrow cells, and positive antinuclear and DNA antibody tests. One year after his first visit, he developed arthritis and maculopapular erythematous rashes. The histologic features of the skin lesions were similar to those of in discoid lupus erythematosus. He was diagnosed as having systemic lupus erythematosus supervening refractory anemia.

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