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巨细胞包涵体病在新生儿和婴儿中较常见。但因巨细胞包涵体病引起再生障碍性贫血尚未见报道。1987年8月我院遇到巨细胞包涵体病并发再生障碍性贫血1例。现报告如下。病历摘要男患,7个月。住院号:181119。足月顺产第二胎,出生时正常。3个月后有微热及腹泻,近1个月高热39℃～40℃,贫血逐渐加重,在院外曾做一次骨穿。骨髓象:骨髓增生低下,红系受抑,粒系减低,淋巴系相对增高,巨核系正常,血小板成堆易见。门诊以“发烧、贫血待查”收住院。查体:发育正常,营养中等,精神烦躁,面色苍白,皮肤
Giant cell inclusion disease is more common in newborns and infants. However, aplastic anemia caused by giant cell inclusion disease has not been reported yet. In August 1987, one case of giant cell inclusion body disease and aplastic anemia was encountered in our hospital. The report is as follows. Male patient history, 7 months. Hospital number: 181119. Full-term follow-up of the second child, normal birth. 3 months after the fever and diarrhea, nearly 1 month fever 39 ℃ ~ 40 ℃, anemia gradually increased in the hospital had a bone wear. Bone marrow: low myeloid hyperplasia, erythroid suppression, decreased myelomonocytic, lymphatic system is relatively high, normal megakaryocyte, platelet heap easily seen. Outpatient to “fever, awaiting investigation,” admitted to hospital. Physical examination: normal development, moderate nutrition, irritability, pale, skin