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一名患血红蛋白S-C病儿童在低海拔地区发生的脾梗死

Splenic infarction at low altitude in a child with hemoglobin S-C disease.

作者信息

Alvarado C S, Wyly B, Buchanan I, Fajman W A

机构信息

Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

Clin Pediatr (Phila). 1988 Aug;27(8):396-9. doi: 10.1177/000992288802700809.

DOI:10.1177/000992288802700809
PMID:3042248
Abstract

We describe a 15-year-old black boy with hemoglobin S-C disease living in Atlanta (altitude 1,034 ft), with no prior history of aircraft or mountain travel, who developed splenic infarction. The clinical picture was characterized by severe left upper quadrant abdominal pain, fever, splenomegaly, and hematologic and scintigraphic evidence of functional asplenia. The diagnosis was suggested by liver/spleen scintigraphy and further confirmed by ultrasonography and computerized tomography (CT) of the spleen. Treatment consisted of analgesics, intravenous fluids, and short-term antibiotic therapy. The child recovered without sequelae.

摘要

我们描述了一名15岁患有血红蛋白S-C病的黑人男孩,他居住在亚特兰大(海拔1034英尺),此前没有乘坐飞机或前往山区旅行的经历,却发生了脾梗死。临床表现为严重的左上腹腹痛、发热、脾肿大,以及血液学和闪烁扫描检查显示的功能性无脾证据。肝/脾闪烁扫描检查提示了诊断,脾脏超声检查和计算机断层扫描(CT)进一步证实了该诊断。治疗包括使用镇痛药、静脉补液和短期抗生素治疗。该患儿康复,未留下后遗症。

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Splenic infarction at low altitude in a child with hemoglobin S-C disease.一名患血红蛋白S-C病儿童在低海拔地区发生的脾梗死
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引用本文的文献

1
Massive splenic infarction in doubly abnormal heterozygous sickling disorders. A new complication of acute splenic sequestration syndrome.双重异常杂合镰状细胞病中的巨大脾梗死。急性脾滞留综合征的一种新并发症。
West J Med. 1991 Nov;155(5):531-2.