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Pure red cell aplasia characterized by erythropoietic maturation arrest. Response to anti-thymocyte globulin.

作者信息

Jacobs A D, Champlin R E, Golde D W

出版信息

Am J Med. 1985 Mar;78(3):515-7. doi: 10.1016/0002-9343(85)90348-1.

DOI:10.1016/0002-9343(85)90348-1
PMID:3919580
Abstract

Pure red cell aplasia is a syndrome characterized by markedly decreased erythropoiesis. On bone marrow examination, there are typically less than 0.5 percent erythroblasts, but sometimes a picture of maturation arrest can be seen. This report describes a patient with maturation arrest of erythropoiesis at the basophilic normoblast stage who had a response to an eight-day course of anti-thymocyte globulin with a return of normal erythropoiesis.

摘要

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