Dermatitis herpetiformis

A chronic autoimmune subepidermal bullous disease characterized by grouped pruritic lesions such as papules, urticarial plaques, erythema, and herpetiform vesiculae, with a predominantly symmetrical distribution on extensor surfaces of the elbows (90%), knees (30%), shoulders, buttocks, sacral region, and face of children and adults. Erosions, excoriations and hyperpigmentation usually follow. It may also appear as a consequence of gluten intolerance.

Hypopituitarism



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PMID (PMCID)
9279521
MALE Middle Aged
Dermatitis herpetiformis cured by hormone replacement for panhypopituitarism.
Spitzweg C, Hofbauer LC, Heufelder AE.
Endocr J. 1997;44(3):437-40.
We report a 53-year-old male with a four-year history of refractory dermatitis herpetiformis associated with hypopituitarism.