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急性自限性再生障碍性贫血综合征,国内外报道极为少见。自1981年至今,国内仅有数例报告。本病特点为:起病急,病情险,伴有严重的感染及不同程度的出血,骨髓增生减低,全血细胞减少,病程自限,预后良好。我们于1992年5月收治一例,报告如下: 病历摘要吕××,女性,15岁,学生。因发热3周于1992年5月1日急诊入院。入院前3周,患者出现发冷、发热,体温高达40℃,经抗感染治疗,间断使用安痛定,体温持续不退。一周前患者出现面部浮肿,伴有恶心、呕吐、腹痛,无尿频、尿痛、少尿。入院后查体:T39.1,Bp12/8。急性重病容,全身皮肤无黄染,左侧
Acute self-limiting aplastic anemia syndrome, domestic and international reports are extremely rare. Since 1981, there have been only a few reports in China. The disease is characterized by: acute onset, the risk of illness, with severe infection and varying degrees of bleeding, reduced myeloproliferation, pancytopenia, duration of self-limiting, good prognosis. We received a case in May 1992, the report is as follows: Medical record summary LV × ×, female, 15 years old, student. Due to fever for 3 weeks in May 1, 1992 emergency admission. Three weeks before admission, the patient developed chills and fever, and the body temperature was as high as 40 ° C. After anti-infective treatment, the analgesic was used intermittently and the body temperature continued to recede. A week ago, the patient developed facial edema accompanied by nausea, vomiting, abdominal pain, frequent urination, dysuria, oliguria. After admission, physical examination: T39.1, Bp12 / 8. Acute serious illness, systemic skin without yellow dye, on the left