ED92.0ICD-11 MMS 2026-01
Hidradenitis suppurativa
Description
Hidradenitis suppurativa is a chronic disease characterised by recurrent, painful, deep-seated, rounded nodules and abscesses due to follicular occlusion with secondary inflammation and destruction of the pilo-sebaceo-apocrine apparatus and extension to the adjacent subcutaneous tissue. Subsequent hypertrophic scarring and suppuration of apocrine gland-bearing skin (axillae, groins, peri-anal and perineal regions) are the main clinical features. Infection and hormonal influence are described but are not the primary pathogenetic factor: the exact aetiology remains unknown. Obesity is common and is associated with more severe disease. The main complications are fistulae, arthropathy, carcinoma and amyloidosis.
Index terms
- Hidradenitis suppurativa
- Acne inversa
- Inverse acne
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- Suppurative hidradenitis
- Hidradenitis suppurativa of axillae
- Acne inversa of axillae
- Hidradenitis suppurativa of anogenital region
- Acne inversa of anogenital region
- Hidradenitis suppurativa affecting other specified sites
- Hidradenitis suppurativa of multiple sites
- Acne inversa of multiple sites
- Hidradenitis suppurativa, atypical forms
Sibling codes
Foundation entity
Hidradenitis suppurativa – http://id.who.int/icd/entity/1621794154
Allowed postcoordination axes
Part of: ED92: Disorders involving the apocrine follicular unit › 14: Diseases of the skin