Synchronous pyoderma gangrenosum and inflammatory bowel disease, healing after total proctocolectomy

Author:

Andrade Pedro1,Brites Maria Manuel1,Figueiredo Américo2

Affiliation:

1. University of Coimbra, Portugal

2. University of Coimbra

Abstract

We present a female patient observed with painful violaceous plaques with central bullae and pustules on the lower limbs, rapidly transformed into ulcers, associated with bloody diarrhea, recurrent oral erosions and hyperthermia in the previous 3 months. Cutaneous biopsy was consistent with pyoderma gangrenosum, and intestinal diagnostic procedures revealed a non-classifiable inflammatory bowel disease with high x-ANCA titers. Soon after admission the patient was submitted to total proctocolectomy following colonic perforation. Complete ulcer healing occurred three months after surgery, without recurrence. Pyoderma gangrenosum is a rare dermatosis frequently associated with inflammatory bowel disease. This case is particularly interesting for the synchronic clinical presentation of cutaneous and intestinal diseases, but also for the prompt regression of the former after total proctocolectomy.

Publisher

FapUNIFESP (SciELO)

Subject

Dermatology

Reference6 articles.

1. Pyoderma gangrenosum: an updated review;Ruocco E;J Eur Acad Dermatol Venereol,2009

2. Pyoderma gangrenosum: a review;Wollina U;Orphanet J Rare Dis,2007

3. Pyoderma gangrenosum: a clinical manifestation of difficult diagnosis;Santos M;An Bras Dermatol,2011

4. Neutrophilic dermatoses: a review of current treatment options;Cohen PR;Am J Clin Dermatol,2009

5. Clinical course and evolution of erythema nodosum and pyoderma gangrenosum in chronic ulcerative colitis;Mir-Madjlessi SH;Am J Gastroenterol,1985

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