Abstract
Henoch-Schönlein purpura (HSP) is a systemic vasculitis that is common in the pediatric population and often presents with the classical triad of palpable purpura, arthralgia, and abdominal pain. We describe a case of HSP in a 14-year-old adolescent girl who presented with atypical features of painful hemorrhagic bullae. The patient was treated with high-dose steroids, dapsone, and supportive therapy with remarkable improvement.
MeSH terms
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Abdominal Pain / etiology*
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Adolescent
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Dapsone / therapeutic use
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Dermatologic Agents / therapeutic use*
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Female
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Follow-Up Studies
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Glucocorticoids / therapeutic use
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Hemorrhage / pathology
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Humans
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IgA Vasculitis / diagnosis*
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IgA Vasculitis / drug therapy
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IgA Vasculitis / pathology
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Skin Diseases, Vesiculobullous / diagnosis
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Skin Diseases, Vesiculobullous / pathology
Substances
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Dermatologic Agents
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Glucocorticoids
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Dapsone