ED92.0

ICD-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
Show allHide
  • 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

  • ED92.1 – Apocrine sweat disorders
  • ED92.Y – Other specified disorders involving the apocrine follicular unit
  • ED92.Z – Disorders involving the apocrine follicular unit, unspecified

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