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[An unusual case of pyoderma gangrenosum with necrotizing granulomatous dermatitis]
Friedegund Meier1, Diana Berner, Christian Scherwitz
1Abteilung für Dermatologie, Universität Tübingen, Tübingen, Deutschland. friedegund.meier@med.uni-tuebingen.de
Abstract:
Four distinctive clinical and histological variants of pyoderma gangrenosum have been proposed: (1) ulcerative, (2) pustular, (3) bullous, and (4) vegetative. The rate of progression and associated systemic diseases, as well as the histopathologic changes, can vary considerably between these clinical variants. A 64-year-old man presented with ulcerative pyoderma gangrenosum associated with renal cell carcinoma and IgA paraproteinemia; he responded to oral thalidomide. Histopathology revealed unusual findings with signs of leukocytoclastic vasculitis, basophilic degeneration of collagen and zones of suppuration with a palisaded histiocytic and epithelioid granulomatous infiltration throughout the dermis.
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