EB21 Pyoderma gangrenosum

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterised by the presence of boggy, purplish ulcers with undermined borders, appearing mostly on the legs. The majority of cases are in people between 40 and 60 years old. Its etiology is unknown.

inclusions

• Phagedenic pyoderma

synonyms

• Pyoderma gangrenosum
• Phagedenic pyoderma
• phagedena geometric
• Pyoderma gangrenosum classified by aetiological associations
• Pyoderma gangrenosum associated with inflammatory bowel disease
• Pyoderma gangrenosum linked to haematological disorder
• Pyoderma gangrenosum associated with inflammatory polyarthropathy
• Pyoderma gangrenosum linked to certain specified identified triggers
• Hidradenitis suppurativa - pyoderma gangrenosum complex
• Pyoderma gangrenosum, acne conglobata and suppurative hidradenitis
• PASH - [pyoderma gangrenosum, acne conglobata and suppurative hidradenitis]
• Pyoderma gangrenosum without identifiable trigger
• Pyoderma gangrenosum classified by clinical type
• Pyoderma gangrenosum, ulcerative
• Pyoderma gangrenosum, classical type
• Pyoderma gangrenosum, bullous
• Pyoderma gangrenosum, atypical
• Pyoderma gangrenosum, pustular
• Pyoderma gangrenosum, atypical pustular
• Pyoderma gangrenosum, superficial vegetating
• Chronic superficial pyoderma
• Superficial granulomatous pyoderma
• Parastomal pyoderma gangrenosum
• Dermatitis gangrenosa

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