Zwerdling T, Finlay J, Glader B E
Clin Pediatr (Phila). 1986 Nov;25(11):563-5. doi: 10.1177/000992288602501104.
This case report describes a 16-year-old girl with pure red cell aplasia of 7 months duration. The erythrocyte characteristics and in vitro culture of erythroid progenitors was similar to that found in transient erythroblastopenia of childhood (TEC), a disorder most commonly seen in children 2 to 6 years of age. This case may represent the adolescent equivalent of TEC.
本病例报告描述了一名患有持续7个月纯红细胞再生障碍性贫血的16岁女孩。红细胞特征及红系祖细胞的体外培养与儿童暂时性红细胞生成减少症(TEC)相似,TEC是一种最常见于2至6岁儿童的疾病。该病例可能代表了青少年期的TEC。