Literature DB >> 3280621

Atrophoderma vermiculatum. Case reports and review.

P J Frosch1, M R Brumage, C Schuster-Pavlovic, A Bersch.   

Abstract

Two patients, a father and a daughter, with atrophoderma vermiculatum are presented. The chief characteristics of this rare, benign condition that usually begins in childhood are a symmetric worm-eaten or reticular atrophy of the cheeks that may extend to the ears or forehead. An autosomal dominant mode of inheritance is present in this family. The prominent characteristics, cause, histologic findings, and rare associated medical conditions are reviewed. The prognosis is good, with many instances of spontaneous regression. Primarily a cosmetic problem, therapy for this condition is aimed at reassurance, genetic counseling, and dermabrasion where appropriate.

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Year:  1988        PMID: 3280621     DOI: 10.1016/s0190-9622(88)70077-8

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  2 in total

1.  A case of atrophoderma vermiculatum responding to systemic isotretinoin.

Authors:  Zoi Apalla; George Karakatsanis; Marina Papageorgiou; Chionati Kastoridou; George Chaidemenos
Journal:  J Dermatol Case Rep       Date:  2009-12-30

2.  A Case of Atrophoderma Vermiculatum Showing a Good Response to Topical Tretinoin.

Authors:  Young Chae Lee; Sook-Ja Son; Tae Young Han; June Hyunkyung Lee
Journal:  Ann Dermatol       Date:  2017-12-26       Impact factor: 1.444

  2 in total

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