PUVA, psoralen with ultraviolet A. Optimal Therapeutic Approach for this Disease The lesions of hyperkeratosis lenticularis perstans are usually asymptomatic but cosmetically frustrating. Reports have noted that older lesions are more resistant to treatment than more recent lesions. Topical treatments are a reasonable first approach. Potent topical steroids class I with or without occlusion can be used in a pulsed 4 x daily a week regimen to minimize side effects of atrophy, and can be considered first-line. Topical retinoids at the highest strength tolerable have been used.
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These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
In-Depth Information The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health.
Visit the website to explore the biology of this condition. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. Access to this database is free of charge. PubMed is a searchable database of medical literature and lists journal articles that discuss Hyperkeratosis lenticularis perstans. Click on the link to view a sample search on this topic. We remove all identifying information when posting a question to protect your privacy.
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Hyperkeratosis lenticularis perstans
The disorder was first described by Flegel summary by Bean, Another member of the family was reported by Bean All 4 affected members in 3 generations had onset between the fourth and seventh decade of scattered reddish-brown discrete papules primarily affecting the extremities but also involving the thighs and trunk. Beveridge and Langlands described 2 generations of a kindred manifesting HLP.
Hyperkeratosis Lenticularis Perstans: Case Report of a Rare Entity
Flegel disease pathology
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