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Accès ouvert déclaré 2010 article

Post-operative pyoderma gangrenosum in association with ileal carcinoid tumour.

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Editor Pyoderma gangrenosum (PG) is an uncommon, progressive ulcerative condition of skin. It presents with deep ulceration characterised by an overhanging violaceous border, which can occur on any body surface. It is frequently confused with other more common ulcerating skin conditions such as necrotising fasciitis, vasculitis, pustular drug reactions and skin infections. Since surgery may be used to treat some of these conditions, but is relatively contraindicated in PG, early diagnosis is critical and is usually made in conjunction with a dermatologist. This 76-year-old male had a laparoscopic assisted right hemi-colectomy for an apparent ascending colonic tumour, however histology actually revealed a well differentiated neuroendocrine tumour of the terminal ileum. Serum pancreatic polypeptide, N and C-terminal glucagon, chromogranin A and urinary 5-HIAA collection were all elevated. On day 7 this man's left iliac fossa port site was noted to be indurated and erythematous. Cefuroxime was empirically commenced for a presumed wound infection. He became pyrexic with a leukocytosis of 30,000 mm3 and skin at the port site quickly became sloughly and ischaemic (Figure 1). Following debridement he required transfer to intensive care as a case of suspected necrotising fasciitis. Fig 1 Early violaceous change around a laparoscopic port site The patient's necrotising skin condition progressed relentlessly. He required 4 further debridement's with intermittent returns to the intensive care unit for supportive therapy (Figure 2). Microbiology of the skin specimens was insignificant and pathology described neutrophillic abscesses with no evidence of vasculitis, granulomatous inflammation or metastatic tumour. Following a dermatological opinion a diagnosis of PG was made. Fig 2 Extensive abdominal wall debridement with classical violaceous borders seen at the wound periphery Intravenous antibiotics were stopped and high dose prednisolone was commenced in addition to the already prescribed somatostatin (Octreotide®). The patient was maintained on azathioprine (Imuran®) once the prednisolone had been tapered. His large abdominal defect was dressed with Activon tulle® honey dressings. He progressed well and was discharged. Follow up revealed satisfactory recovery of the wound.

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Sujets associés

Autoimmune and Inflammatory DisordersHidradenitis Suppurativa and TreatmentsAutoimmune Bullous Skin Diseases

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