4A43.4

ICD-11 MMS 2026-01

Diffuse eosinophilic fasciitis

Description

Also called Shulman disease/diffuse fasciitis, diffuse eosinophilic fasciitis is a rare idiopathic disorder associated with induration of the skin (orange-peel sign) that generally develops rapidly. It is a dermal and hypodermal sclerosis associated with fibrotic thickening of the subcutaneous adipose lobular septa, superficial fascia, and perimysium. Full thickness excisional biopsy of skin lesions revealing fibrosis of the subcutaneous fascia is generally required for diagnosis. Onset follows unusual physical exertion and trauma, especially in males.

Index terms

  • Diffuse eosinophilic fasciitis
  • Diffuse fasciitis
  • Eosinophilic fasciitis
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  • Fasciitis with eosinophilia syndrome
  • Shulman syndrome

Exclusions from above levels

  • 02 – Neoplasms
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 20 – Developmental anomalies

Sibling codes

  • 4A43.0 – IgG4 related disease
  • 4A43.1 – Mikulicz disease
  • 4A43.2 – Sjögren syndrome
  • 4A43.3 – Mixed connective tissue disease
  • 4A43.Y – Other specified overlap non-organ specific systemic autoimmune disease
  • 4A43.Z – Undifferentiated non-organ specific systemic autoimmune disease

Foundation entity

Diffuse eosinophilic fasciitis – http://id.who.int/icd/entity/1977389237

Part of: 4A43: Overlap or undifferentiated nonorgan specific systemic autoimmune disease › 04: Diseases of the immune system