A rare case of familial reactive perforating collagenosis

Reactive perforating collagenosis (RPC) is a rare disorder of transepidermal elimination in which genetically altered collagen is extruded out through the epidermis. This disease usually starts as asymptomatic or pruritic umbilicated papules on extensor aspects of extremities and face, and the lesio...

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Main Authors: Anup Kumar Tiwary, Dharmendra K Mishra, Shyam S Chaudhary
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Paediatric Dermatology
Subjects:
Online Access:http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=230;epage=233;aulast=Tiwary
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author Anup Kumar Tiwary
Dharmendra K Mishra
Shyam S Chaudhary
author_facet Anup Kumar Tiwary
Dharmendra K Mishra
Shyam S Chaudhary
author_sort Anup Kumar Tiwary
collection DOAJ
description Reactive perforating collagenosis (RPC) is a rare disorder of transepidermal elimination in which genetically altered collagen is extruded out through the epidermis. This disease usually starts as asymptomatic or pruritic umbilicated papules on extensor aspects of extremities and face, and the lesions become more conspicuous with age. It has two forms: Acquired and inherited form, of which inherited form is extremely rare. Here, we document a case of inherited form of RPC in a 13-year-old boy having multiple asymptomatic hyperpigmented umbilicated papules with a central keratotic plug distributed chiefly over face and extensor aspect of upper and lower extremities since his infancy, with history of similar lesions in his 18-year-old elder brother.
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spelling doaj.art-bd90f205376a4e46b9b24045784490882022-12-22T01:52:44ZengWolters Kluwer Medknow PublicationsIndian Journal of Paediatric Dermatology2319-72502017-01-0118323023310.4103/2319-7250.184436A rare case of familial reactive perforating collagenosisAnup Kumar TiwaryDharmendra K MishraShyam S ChaudharyReactive perforating collagenosis (RPC) is a rare disorder of transepidermal elimination in which genetically altered collagen is extruded out through the epidermis. This disease usually starts as asymptomatic or pruritic umbilicated papules on extensor aspects of extremities and face, and the lesions become more conspicuous with age. It has two forms: Acquired and inherited form, of which inherited form is extremely rare. Here, we document a case of inherited form of RPC in a 13-year-old boy having multiple asymptomatic hyperpigmented umbilicated papules with a central keratotic plug distributed chiefly over face and extensor aspect of upper and lower extremities since his infancy, with history of similar lesions in his 18-year-old elder brother.http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=230;epage=233;aulast=TiwaryReactive perforating collagenosistransepidermal eliminationumbilicated
spellingShingle Anup Kumar Tiwary
Dharmendra K Mishra
Shyam S Chaudhary
A rare case of familial reactive perforating collagenosis
Indian Journal of Paediatric Dermatology
Reactive perforating collagenosis
transepidermal elimination
umbilicated
title A rare case of familial reactive perforating collagenosis
title_full A rare case of familial reactive perforating collagenosis
title_fullStr A rare case of familial reactive perforating collagenosis
title_full_unstemmed A rare case of familial reactive perforating collagenosis
title_short A rare case of familial reactive perforating collagenosis
title_sort rare case of familial reactive perforating collagenosis
topic Reactive perforating collagenosis
transepidermal elimination
umbilicated
url http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=230;epage=233;aulast=Tiwary
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