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Life-threatening or organ-impairing Henoch-Schönlein purpura: plasmapheresis may save lives and limit organ damage.

作者信息

Donghi Davide, Schanz Urs, Sahrbacher Ulrike, Recher Mike, Trüeb Ralph M, Müllhaupt Beat, French Lars E, Hafner Jürg

机构信息

Department of Dermatology, University Hospital of Zürich, Zürich, Switzerland.

出版信息

Dermatology. 2009;219(2):167-70. doi: 10.1159/000223237. Epub 2009 Jun 2.

Abstract

Adult-onset Henoch-Schonlein purpura (HSP) tends to become chronic-relapsing, yet rarely leads to organ impairment, e.g. due to chronic glomerulonephritis. Bed rest, compression and nonsteroidal anti-inflammatory drugs are usually sufficient to control the active phases. We report 2 cases of adult HSP with an unusually severe evolution. One patient required intensive-care treatment for hypovolemic shock caused by hemorrhagic pancolitis; the other had progressive and extremely extensive vasculitic leg ulcers. Both were refractory to common immunosuppression with systemic corticosteroids (oral and pulse) and additive steroid-sparing immunosuppressive drugs. Only after the introduction of plasmapheresis did both patients show a dramatic improvement in the disease, with rapid and almost complete healing. Plasmapheresis is a rarely used therapeutic tool in the treatment of severe HSP, but the growing literature on its highly beneficial effect underlines its potential usefulness.

摘要

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