Abstract
Henoch-Schönlein purpura (HSP) is a readily recognizable clinical syndrome familiar to most physicians and characterized by the appearance of a vasculitic rash especially on the legs and buttocks, flitting arthropathy, gastrointestinal problems, and glomerulonephritis. The introduction of immunofluorescence studies of renal biopsies brought confirmation of the immunologic nature of the pathologic lesions and the remarkable similarity between the renal lesion of HSP and IgA nephropathy. This chapter explores the differences and similarities between the two conditions and points strongly to a concept of unity. To this time, however, this concept is not proved; proof probably awaits a specific diagnostic test similar to the L.E. cell or antinuclear antibody test in systemic lupus erythematosus.
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© 1987 Martinus Nijhoff Publishing, Boston
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Clarkson, A.R. (1987). Henoch-Schönlein Purpura and IgA Nephropathy: To Separate or Unify?. In: Clarkson, A.R. (eds) IgA Nephropathy. Topics in Renal Medicine, vol 2. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2039-5_4
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DOI: https://doi.org/10.1007/978-1-4613-2039-5_4
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