硫胺素反应性巨幼细胞贫血综合征中的红细胞生成异常和骨髓发育异常。
Dyserythropoiesis and myelodysplasia in thiamine-responsive megaloblastic anemia syndrome.
作者信息
Faraji-Goodarzi Mojgan, Tarhani Fariba, Taee Nadereh
机构信息
Department of Pediatrics Faculty of Medicine Lorestan University of Medical Sciences Khorramabad Iran.
出版信息
Clin Case Rep. 2020 Mar 6;8(6):991-994. doi: 10.1002/ccr3.2791. eCollection 2020 Jun.
Abstract
The case of thiamine-responsive megaloblastic anemia (TRMA) presented here speculates the need early diagnosis, continuous monitoring, follow-up, and regulated treatment plan for the patients. Complications and systemic manifestations are likely to enhance in otherwise circumstances.
摘要
本文所呈现的硫胺素反应性巨幼细胞贫血（TRMA）病例提示，对于患者而言，需要进行早期诊断、持续监测、随访以及制定规范的治疗方案。在其他情况下，并发症和全身表现可能会加重。
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