LETTER TO EDITOR
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|Year : 2004 | Volume
| Issue : 5 | Page : 317
Dermatological findings in chronic alcoholics
Department of Neurological Sciences, Christian Medical College, Vellore - 632 004, India
Department of Neurological Sciences, Christian Medical College Hospital, Vellore - 632004, Tamilnadu
|How to cite this article:|
Kumar S. Dermatological findings in chronic alcoholics.Indian J Dermatol Venereol Leprol 2004;70:317-317
|How to cite this URL:|
Kumar S. Dermatological findings in chronic alcoholics. Indian J Dermatol Venereol Leprol [serial online] 2004 [cited 2020 Sep 25 ];70:317-317
Available from: http://www.ijdvl.com/text.asp?2004/70/5/317/12850
I read with great interest the recent article by Dr. G.S. Rao describing the changes in the skin, nails, hair and oral cavity.
The author's efforts are commendable. However, I would like to make certain observations and draw attention to other dermatological manifestations in alcoholics not reported by the author. These include type I allergic skin manifestations, palmoplantar hyperhidrosis (PPH), spontaneous skin necrosis, and increased risk of basal cell carcinoma (BCC). Allergic skin manifestations in alcoholics occur due to a combination of a direct effect of alcohol and an indirect effect through elevation of IgE. Alcoholics are frequently noted to have PPH. As the findings of peripheral nerve conduction (sympathetic skin responses) studies do not differ between alcoholics with PPH and those with primary PPH, hyperhidrosis is believed to occur due to impaired central sweat control mechanisms. In a large prospective cohort study, the total alcohol and white wine intake were associated with a higher risk of occurrence of BCC in both men and women.
In addition, chronic alcohol consumption affects the clinical presentation and treatment responsiveness of certain dermatological conditions. Excess alcohol consumption is associated with the onset and flare-up of psoriasis and discoid eczema. Alcoholism also leads to a poor response to anti-psoriatic treatment, and contributes to an excess mortality in patients with psoriasis.
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