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再生障碍性贫血诊断后发生的慢性冷凝集素病

[Chronic cold agglutinin disease occurring after a diagnosis of aplastic anemia].

作者信息

Su C Y, Arai N, Umeda M, Shirai T

机构信息

First Department of Internal Medicine, Toho University School of Medicine, Tokyo.

出版信息

Rinsho Ketsueki. 1992 Jan;33(1):36-41.

PMID:1545514
Abstract

We report herein a 61-year-old man with chronic cold agglutinin disease which occurred after a diagnosis of aplastic anemia. The patient's pancytopenia was recognized upon visiting a local doctor because of high fever and cough on December 21, 1985. He was subsequently admitted to our hospital because of anasarca on January 31, 1986, and was diagnosed as having aplastic anemia. He was treated with prednisolone, and was discharged after his anemia improved. He was readmitted on October 23, 1988, because of icterus. Laboratory data on the patients second admission revealed increased reticulocyte count, hyperplastic bone marrow with a predominance of erythroblasts, increased serum indirect bilirubin, increased serum LDH1 value and decreased serum haptoglobin. Moreover, cold agglutinin titer was increased, anti-IF antibody was positive, and anti-IgM antibody was recognized with direct anti-globulin test. There was no precedent infection such as mycoplasma pneumonia or infectious mononucleosis. Hence, this patient was diagnosed as having chronic cold agglutinin disease.

摘要

我们在此报告一名61岁男性,其慢性冷凝集素病发生于再生障碍性贫血诊断之后。该患者于1985年12月21日因高热和咳嗽就诊于当地医生时被发现全血细胞减少。随后,他于1986年1月31日因全身性水肿入住我院,并被诊断为再生障碍性贫血。他接受了泼尼松龙治疗,贫血改善后出院。1988年10月23日,他因黄疸再次入院。患者第二次入院时的实验室检查数据显示网织红细胞计数增加、骨髓增生以成红细胞为主、血清间接胆红素升高、血清LDH1值升高和血清结合珠蛋白降低。此外,冷凝集素滴度升高,抗IF抗体阳性,直接抗球蛋白试验可识别抗IgM抗体。没有支原体肺炎或传染性单核细胞增多症等前驱感染。因此,该患者被诊断为慢性冷凝集素病。

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