EB40.2

ICD-11 MMS 2026-01

Paraneoplastic pemphigus

Description

Paraneoplastic pemphigus is a severe, often fatal autoimmune disease characterised by blisters and erosions not only on the skin and the mucous membranes but also involving other organs including the respiratory system. Auto-antibodies to a variety of plakin components of desmosomes and hemidesmosomes and to the protease inhibitor, Alpha-2-macroglobulin-like-1 protein, have all been implicated in its pathogenesis. It is strongly associated with lymphoproliferative disease.

Index terms

  • Paraneoplastic pemphigus

Exclusions from above levels

  • 1B72.0 – Bullous impetigo of the napkin area
  • 1F23.12 – Napkin candidosis
  • EH71 – Dermatoses precipitated by drug therapy
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  • EH76 – Dermatoses associated with specific classes of medication

Sibling codes

  • EB40.0 – Pemphigus vulgaris
  • EB40.1 – Pemphigus foliaceus
  • EB40.Y – Other specified pemphigus
  • EB40.Z – Pemphigus, unspecified

Foundation entity

Paraneoplastic pemphigus – http://id.who.int/icd/entity/104197957

Allowed postcoordination axes

Part of: EB40: Pemphigus › 14: Diseases of the skin