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Papular elastorrhexis: clinical perspectives

Authors Sezer E, Durmaz EÖ, Şahin S

Received 28 April 2018

Accepted for publication 2 August 2018

Published 26 October 2018 Volume 2018:11 Pages 541—544

DOI https://doi.org/10.2147/CCID.S151020

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Jeffrey Weinberg


Engin Sezer, Emel Öztürk Durmaz, Sedef Şahin

Department of Dermatology, Acibadem University School of Medicine, Istanbul, Turkey

Abstract: First described by Bordas in 1987, papular elastorrhexis (PE) is a rare elastic fiber disorder of the skin characterized by multiple, discrete, asymptomatic, firm, nonfollicular, monomorphous, 1–5 mm, circumscribed, hypopigmented, oval to round papules, symmetrically distributed on the chest, abdomen, back, shoulders, arms, and thighs. The onset of the condition is usually in the first or second decade of life. PE appears to be an exceedingly rare entity, with 33 cases reported in the literature until now. However, the disorder might be underestimated probably because of its subtlety, asymptomatic course, and benign nature of clinical alterations, which can easily be confused with other dermatoses such as acne scars. Clinical and histopathological differential diagnosis of PE is broad and includes papular acne scars, eruptive collagenoma, disseminated lenticular dermatofibrosis (as a component of Buschke–Ollendorff syndrome), white fibrous papulosis of the neck, pseudoxanthoma elasticum, pseudoxanthoma elasticum-like papillary dermal elastolysis, middermal elastolysis, and perifollicular elastolysis. Treatment of PE is a matter of debate and no reliable curative option exists.

Keywords: papular elastorrhexis, elastic fibers, connective tissue

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