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特发性纯红细胞再生障碍:病例报告并文献复习

Idiopathic pure red cell aplasia: case report with review of literature.

作者信息

Khalife Wissam, Murunga Eric, Mahmoud Fade

机构信息

U.S.D. School of Medicine, Internal Medicine Residency Program, Sioux Falls, SD, USA.

出版信息

S D J Med. 2005 Dec;58(12):501-5.

Abstract

Pure red cell aplasia (PRCA) is characterized by near absence of red blood cell precursors in the bone marrow with associated anemia and reticulocytopenia. Megakaryocytes and white blood cell precursors remain intact. Acute self-limited PRCA is the most common form. Acquired chronic PRCA is often idiopathic but can be associated with underlying disorders such as thymoma or autoimmune diseases. Congenital PRCA is associated with physical abnormalities. Pure red blood cell aplasia should always be included in the differential diagnosis of chronic unexplained anemia. We report a case of idiopathic pure red blood cell aplasia in an elderly male who has had a chronic anemia with recurrent blood transfusions for about 30 years.

摘要

纯红细胞再生障碍性贫血(PRCA)的特征是骨髓中几乎没有红细胞前体,伴有贫血和网织红细胞减少。巨核细胞和白细胞前体保持完整。急性自限性PRCA是最常见的形式。获得性慢性PRCA通常是特发性的,但可能与潜在疾病如胸腺瘤或自身免疫性疾病有关。先天性PRCA与身体异常有关。纯红细胞再生障碍性贫血应始终纳入慢性不明原因贫血的鉴别诊断中。我们报告一例老年男性特发性纯红细胞再生障碍性贫血病例,该患者患有慢性贫血,反复输血约30年。

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