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Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)

Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands. The parents are non-consanguineous and none of his f...

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Autores principales: Bukhari, Rahaf, Alhawsawi, Waseem, Radin, Aisha Ahmad, Jan, Hawazin D., Al Hawsawi, Khalid, Al Ahmadi, Marwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873031/
https://www.ncbi.nlm.nih.gov/pubmed/31762743
http://dx.doi.org/10.1159/000503337
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author Bukhari, Rahaf
Alhawsawi, Waseem
Radin, Aisha Ahmad
Jan, Hawazin D.
Al Hawsawi, Khalid
Al Ahmadi, Marwan
author_facet Bukhari, Rahaf
Alhawsawi, Waseem
Radin, Aisha Ahmad
Jan, Hawazin D.
Al Hawsawi, Khalid
Al Ahmadi, Marwan
author_sort Bukhari, Rahaf
collection PubMed
description Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands. The parents are non-consanguineous and none of his family members had similar lesions. Skin examination revealed multiple tiny keratotic pits on both palms. Punch skin biopsy from the palmar lesion revealed epidermal depression with an overlying column of compact orthokeratosis. Based on the above clinicopathological findings, a diagnosis of punctate palmoplantar keratoderma type 1 was made. The patient was started on 40% urea and 20% salicylic acid ointment for months but with little improvement.
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spelling pubmed-68730312019-11-22 Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease) Bukhari, Rahaf Alhawsawi, Waseem Radin, Aisha Ahmad Jan, Hawazin D. Al Hawsawi, Khalid Al Ahmadi, Marwan Case Rep Dermatol Single Case Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands. The parents are non-consanguineous and none of his family members had similar lesions. Skin examination revealed multiple tiny keratotic pits on both palms. Punch skin biopsy from the palmar lesion revealed epidermal depression with an overlying column of compact orthokeratosis. Based on the above clinicopathological findings, a diagnosis of punctate palmoplantar keratoderma type 1 was made. The patient was started on 40% urea and 20% salicylic acid ointment for months but with little improvement. S. Karger AG 2019-10-10 /pmc/articles/PMC6873031/ /pubmed/31762743 http://dx.doi.org/10.1159/000503337 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case
Bukhari, Rahaf
Alhawsawi, Waseem
Radin, Aisha Ahmad
Jan, Hawazin D.
Al Hawsawi, Khalid
Al Ahmadi, Marwan
Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title_full Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title_fullStr Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title_full_unstemmed Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title_short Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
title_sort punctate palmoplantar keratoderma: a case report of type 1 (buschke-fischer-brauer disease)
topic Single Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873031/
https://www.ncbi.nlm.nih.gov/pubmed/31762743
http://dx.doi.org/10.1159/000503337
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