医学
川崎病
万古霉素
冠状动脉疾病
外科
动脉
内科学
金黄色葡萄球菌
生物
细菌
遗传学
出处
期刊:Archives of Dermatology
[American Medical Association]
日期:1988-08-01
卷期号:124 (8): 1186-1188
被引量:21
标识
DOI:10.1001/archderm.124.8.1186
摘要
To the Editor.—
Linear IgA bullous dermatosis (LABD) is an idiopathic vesiculobullous disease with a nondiagnostic clinical appearance. It is best characterized pathologically by subepidermal bullous formation with homogeneous linear IgA deposition at the blister base.1-4Although LABD is most often idiopathic, drug-induced disease may occur rarely.5,6We describe a patient with vancomycin-induced LABD in whom the eruption was documented clinically, histopathologically, and immunologically on rechallenge. Report of a Case.—
A 68-year-old man with coronary artery disease was admitted to the New England Deaconess Hospital (Boston) for a coronary artery bypass graft. On admission, his medications included atenolol, diltiazem hydrochloride, tolazamide (Tolinase) nitropaste, intravenous heparin, digoxin, and prazosin hydrochloride. There was no history of drug allergy. On hospital day 2, the patient underwent coronary artery bypass grafting, which was complicated by cardiogenic shock and acute tubular necrosis. An intra-aortic balloon pump and atrioventricular pacing was needed. Intravenously administered
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