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F. Dabouz on Muck Rack

F. Dabouz

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Comorbidities of pyoderma gangrenosum: a retrospective multicentric analysis of 126 patients

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By P. Senet, C. Debure, P. Bernard, M. Gillard, D. Anuset, H. Maillard, J. F. Cuny, E. Mahe, C. Sin, F. Dessiner, E. Goujon, J. Journet-Tollhupp, F. Dabouz, T. Develter, C. Lok, P. Modiano
| Color Research & Application Verified
Pyoderma Grangrenosum (PG) is a rare neutrophilic dermatosis with challenging diagnosis and unclear underlying mechanisms. Multifactorial causes are purposed, including neutrophilic dysfunction, aberrant cellular immunity and cytokinic activities, and genetic predispositions1. An association with a systemic disease is classically described in 25 to 75% of cases, including inflammatory bowel diseases (IBD), inflammatory rheumatological diseases (IRD) and hematological disorders.
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