4A43.4ICD-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
Sibling codes
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