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患有大疱性肥大细胞增多症的婴儿发生休克。

Shock in an infant with bullous mastocytosis.

作者信息

Poterack C D, Sheth K J, Henry D P, Eisenberg C

机构信息

Department of Pediatrics, Medical College of Wisconsin, Milwaukee 53226.

出版信息

Pediatr Dermatol. 1989 Jun;6(2):122-5. doi: 10.1111/j.1525-1470.1989.tb01009.x.

Abstract

A 6-month-old infant had bullous lesions on his posterior neck, upper trunk, and extremities for two months prior to admission for fever and shock. He had an elevated white blood cell count with left shift and normal platelet count, but abnormal coagulation studies. He was treated with intravenous antibiotics, crystalloids, fresh-frozen plasma, and pressor agents. A histamine H2 receptor antagonist was started for guaiac-positive nasogastric tube drainage. The patient recovered after four days of treatment. A skin biopsy confirmed mastocytosis. A week later the child passed grossly bloody stools with blood clots. No source of gastrointestinal bleeding was identified by extensive work-up. Blood histamine level measured one day before gastrointestinal bleeding was 16,400 pg/ml (normal 263 +/- 202 pg/ml). The bleeding resolved spontaneously. The patient was maintained on cimetidine. Results of a subsequent bone scan were normal. Shock or gastrointestinal bleeding associated with unusual skin lesions should alert the pediatrician to the possibility of mastocytosis.

摘要

一名6个月大的婴儿在因发热和休克入院前两个月,后颈部、上躯干和四肢出现大疱性病变。他白细胞计数升高伴核左移,血小板计数正常,但凝血研究异常。给予静脉抗生素、晶体液、新鲜冷冻血浆和升压药治疗。因鼻胃管引流隐血阳性开始使用组胺H2受体拮抗剂。治疗四天后患者康复。皮肤活检证实为肥大细胞增多症。一周后,患儿排出带有血凝块的肉眼可见的血便。广泛检查未发现胃肠道出血的来源。胃肠道出血前一天测得的血组胺水平为16400 pg/ml(正常为263±202 pg/ml)。出血自行缓解。患者继续服用西咪替丁。随后的骨扫描结果正常。与异常皮肤病变相关的休克或胃肠道出血应提醒儿科医生注意肥大细胞增多症的可能性。

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