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未被怀疑的恶性贫血并发镰状细胞β地中海贫血导致的全血细胞减少症。

Pancytopenia caused by unsuspected pernicious anemia complicating sickle cell beta-thalassemia.

作者信息

Chen M C, Koshy M, Kennedy J

机构信息

Department of Medicine, University of Illinois, Chicago 60612.

出版信息

South Med J. 1992 Feb;85(2):215-6. doi: 10.1097/00007611-199202000-00028.

Abstract

We have described a a 23-year-old black woman with sickle cell beta-thalassemia who had a urinary tract infection and who was incidentally found to be pancytopenic. Although her anemia was categorized as "normocytic, normochromic" by an electronic particle counter, evaluation of the pancytopenia confirmed unsuspected pernicious anemia. Greater vigilance and a higher index of suspicion are crucial for early diagnosis of pernicious anemia in patients with other known hemoglobinopathies.

摘要

我们描述了一名23岁的镰状细胞β地中海贫血黑人女性,她患有尿路感染,偶然发现全血细胞减少。尽管通过电子粒子计数器将她的贫血分类为“正细胞、正色性”,但对全血细胞减少的评估证实存在未被怀疑的恶性贫血。提高警惕和更高的怀疑指数对于早期诊断患有其他已知血红蛋白病的患者的恶性贫血至关重要。

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