Stevens-Johnson syndrome complicated by fatal hemophagocytic lymphohistiocytosis

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Pancytopenia as an early indicator for Stevens-Johnson syndrome complicated with hemophagocytic lymphohistiocytosis: a case report

BACKGROUND Stevens-Johnson syndrome (SJS) is a severe skin and mucosal bullous disease. When complicated with Hemophagocytic lymphohistiocytosis (HLH), the condition is especially life-threatening. CASE PRESENTATION Here we report the case of a 4-year-old boy suffering from SJS with extensive erythema multiforme and bulla. Despite active intervention and supportive care, the boy experienced i...

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ژورنال

عنوان ژورنال: JAAD Case Reports

سال: 2019

ISSN: 2352-5126

DOI: 10.1016/j.jdcr.2019.07.022