论文部分内容阅读
纯红细胞再生障碍性贫血(Pure redcell aplasia)简称纯红再障。其临床特征为重度贫血,网织红细胞缺乏或显著减少,骨髓红细胞系统增生极度低下,而粒细胞巨核细胞系统无异常,周围血白细胞和血小板计数正常或大致正常。1938年Diamond和B-1ackfan二氏将本病作一独立疾病报告以来,国外已报告100余例,国内1958年彭氏首次报告二例,近年来报告陆续增多,我院自1973年至1982年收治三例先天性纯红再障和一例后天获得性纯红再障报告如下: 病例介绍例一:女,九个月,因出生后皮肤渐苍白,近二个月来加重住院。患儿第四胎,足月顺产,家属无类似病史。体检:营养低下,皮肤粘膜显著苍白,未见出血点及黄
Pure red cell aplasia (pure red aplasia) referred to pure red aplasia. The clinical features of severe anemia, reticulocyte deficiency or significantly reduced bone marrow erythrocyte hyperplasia is extremely low, while no abnormalities of granulocyte megakaryocyte system, peripheral white blood cell and platelet count normal or roughly normal. 1938 Diamond and B-1ackfan two’s disease as an independent disease report since the report of more than 100 cases have been reported abroad, the first report in 1958 Peng’s first two cases in recent years, reports have increased in our hospital from 1973 to 1982 Three cases of congenital pure aplastic anemia and one acquired acquired pure aplastic anemia were reported as follows: Case Description Example 1: Female, nine months old, the skin became pale due to the birth, and the hospitalization was aggravated in the past two months. Children with the fourth child, full-term delivery, no similar family history. Physical examination: low nutrition, skin mucosa was significantly pale, no bleeding and yellow