Skip to
  1. Homepage
  2. Rare diseases
  3. Search
PrintPrint
Simple search

Simple search

*
(*) mandatory field





Other search option(s)

Dermatitis herpetiformis

Orpha number ORPHA1656
Prevalence of rare diseases 1-5 / 10 000
Inheritance
  • Sporadic
Age of onset Variable
ICD 10 code
  • L13.0
MIM number
Synonym(s) Durhing-Brocq disease

Summary

Dermatitis herpetiformis (DH) is a subepidermal bullous disease characterized by chronic recurrence of itchy, erythematous papules, urticarial wheals and grouped vesicles that appear symmetrically on the extensor surfaces, buttocks and back. Children and young adults are mostly affected. Prevalence is estimated about 1 to 4 cases/10 000, with incidence ranging from 0,9 (Italy) to 2,6 (Northern Ireland) new cases/100 000/year. The disease is the cutaneous expression of a gluten-sensitive enteropathy identifiable with celiac disease. The clinical and histological pictures of both entities are quite similar. Granular IgA deposits at the dermo-epidermal junction, neutrophils and eosinophils together with activated CD4+ Th2 lymphocytes are supposed to represent the main immune mechanisms that co-operate in the pathogenesis of the disease. A strict gluten withdrawal from diet represents the basis for treatment. *Authors: Prof. P. Fabbri and Prof. M. Caproni (February 2005)*.

Detailed information

Review article
Get Acrobat Reader
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Languages :