Fabry disease previously diagnosed as Henoch-Schonlein purpura
Henoch-Schonlein purpura (HSP) is a generalized vasculitis characterized by manifestations of the skin, joints, gastrointestinal tract, and renal involvement. Although HSP can occur at any age and is usually a self-limited disease in children, it is less common and has a poor prognosis in adults. Re...
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Veröffentlicht in: | The Korean journal of internal medicine 2015, 30(6), , pp.925-927 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Henoch-Schonlein purpura (HSP) is a generalized vasculitis characterized by manifestations of the skin, joints, gastrointestinal tract, and renal involvement.
Although HSP can occur at any age and is usually a self-limited disease in children, it is less common and has a poor prognosis in adults. Renal involvement affects approximately one-third of HSP patients, and varies from intermittent hematuria and proteinuria, to severe nephrotic-nephritic syndrome with kidney histology being identical to that of immunoglobin A (IgA) nephropathy. KCI Citation Count: 2 |
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ISSN: | 1226-3303 2005-6648 |
DOI: | 10.3904/kjim.2015.30.6.925 |