Familial dyskeratotic comedones: A rare entity

Familial dyskeratotic comedones is an inherited disorder with distinctive clinical features and a disease course that is refractory to treatment. It is clinically characterized by numerous, discrete, disseminate, hyperkeratotic papules and comedones. On histopathology, it shows crater-like invaginat...

Descripción completa

Detalles Bibliográficos
Autores principales: Maddala, Raghu Ram, Ghorpade, Ashok, Polavarpu, Mercy, Adulkar, Satish A., Das, Manbendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763581/
https://www.ncbi.nlm.nih.gov/pubmed/26953840
http://dx.doi.org/10.4103/2229-5178.174308
_version_ 1782417290626596864
author Maddala, Raghu Ram
Ghorpade, Ashok
Polavarpu, Mercy
Adulkar, Satish A.
Das, Manbendra
author_facet Maddala, Raghu Ram
Ghorpade, Ashok
Polavarpu, Mercy
Adulkar, Satish A.
Das, Manbendra
author_sort Maddala, Raghu Ram
collection PubMed
description Familial dyskeratotic comedones is an inherited disorder with distinctive clinical features and a disease course that is refractory to treatment. It is clinically characterized by numerous, discrete, disseminate, hyperkeratotic papules and comedones. On histopathology, it shows crater-like invaginations filled with keratinous material and evidence of dyskeratosis. We report here one family from central India with this rare disorder.
format Online
Article
Text
id pubmed-4763581
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-47635812016-03-07 Familial dyskeratotic comedones: A rare entity Maddala, Raghu Ram Ghorpade, Ashok Polavarpu, Mercy Adulkar, Satish A. Das, Manbendra Indian Dermatol Online J Case Report Familial dyskeratotic comedones is an inherited disorder with distinctive clinical features and a disease course that is refractory to treatment. It is clinically characterized by numerous, discrete, disseminate, hyperkeratotic papules and comedones. On histopathology, it shows crater-like invaginations filled with keratinous material and evidence of dyskeratosis. We report here one family from central India with this rare disorder. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4763581/ /pubmed/26953840 http://dx.doi.org/10.4103/2229-5178.174308 Text en Copyright: © 2016 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Maddala, Raghu Ram
Ghorpade, Ashok
Polavarpu, Mercy
Adulkar, Satish A.
Das, Manbendra
Familial dyskeratotic comedones: A rare entity
title Familial dyskeratotic comedones: A rare entity
title_full Familial dyskeratotic comedones: A rare entity
title_fullStr Familial dyskeratotic comedones: A rare entity
title_full_unstemmed Familial dyskeratotic comedones: A rare entity
title_short Familial dyskeratotic comedones: A rare entity
title_sort familial dyskeratotic comedones: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763581/
https://www.ncbi.nlm.nih.gov/pubmed/26953840
http://dx.doi.org/10.4103/2229-5178.174308
work_keys_str_mv AT maddalaraghuram familialdyskeratoticcomedonesarareentity
AT ghorpadeashok familialdyskeratoticcomedonesarareentity
AT polavarpumercy familialdyskeratoticcomedonesarareentity
AT adulkarsatisha familialdyskeratoticcomedonesarareentity
AT dasmanbendra familialdyskeratoticcomedonesarareentity

Ejemplares similares