Acquired anhidrosis a case report
V Laxmi Nair
|How to cite this article:
Nair V L, Beena D, Ram S M. Acquired anhidrosis a case report. Indian J Dermatol Venereol Leprol 1992;58:111-112
AbstractA 30-year -old man was seen for acquired anhidrosis. There was no systemic disease. Vasomotor functions were normal. Biopsy showed normal sweat glands and ducts. Intravenous injection of neostigmine could produce profuse sweating on the face, trunk and arms. The disorder is likely to be due to a peripheral dysautonomia selectively affecting the sudomotor function.