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Adult-Onset Unilateral Disabling Pansclerotic Morphea

Disabling pansclerotic morphea (DPM) is a rare, severe, and mutilating form of morphea, involving the dermis, subcutaneous tissue, fat, muscle, and even bone. It is usually seen before the age of 14 years, with the patient complaining of arthralgia and stiffness at the time of onset. We report a cas...

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Autores principales: Singh, Adarshlata, Singhal, Kritika, Choudhary, Sanjiv, Bisati, Shazia, Arora, Mallika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037973/
https://www.ncbi.nlm.nih.gov/pubmed/24891683
http://dx.doi.org/10.4103/0019-5154.131459
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author Singh, Adarshlata
Singhal, Kritika
Choudhary, Sanjiv
Bisati, Shazia
Arora, Mallika
author_facet Singh, Adarshlata
Singhal, Kritika
Choudhary, Sanjiv
Bisati, Shazia
Arora, Mallika
author_sort Singh, Adarshlata
collection PubMed
description Disabling pansclerotic morphea (DPM) is a rare, severe, and mutilating form of morphea, involving the dermis, subcutaneous tissue, fat, muscle, and even bone. It is usually seen before the age of 14 years, with the patient complaining of arthralgia and stiffness at the time of onset. We report a case of unilateral adult-onset DPM with sparing of the face. Within a few months of onset, painful contracture deformities of the hand, elbow, and shoulder joints developed, impairing the patient's normal daily activities. We are reporting this case because of the unusual presentation: DPM in an adult, with history of trauma in childhood and rapid onset of complications, is rare.
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spelling pubmed-40379732014-06-02 Adult-Onset Unilateral Disabling Pansclerotic Morphea Singh, Adarshlata Singhal, Kritika Choudhary, Sanjiv Bisati, Shazia Arora, Mallika Indian J Dermatol E-Case Report Disabling pansclerotic morphea (DPM) is a rare, severe, and mutilating form of morphea, involving the dermis, subcutaneous tissue, fat, muscle, and even bone. It is usually seen before the age of 14 years, with the patient complaining of arthralgia and stiffness at the time of onset. We report a case of unilateral adult-onset DPM with sparing of the face. Within a few months of onset, painful contracture deformities of the hand, elbow, and shoulder joints developed, impairing the patient's normal daily activities. We are reporting this case because of the unusual presentation: DPM in an adult, with history of trauma in childhood and rapid onset of complications, is rare. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4037973/ /pubmed/24891683 http://dx.doi.org/10.4103/0019-5154.131459 Text en Copyright: © Indian Journal of Dermatology 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle E-Case Report
Singh, Adarshlata
Singhal, Kritika
Choudhary, Sanjiv
Bisati, Shazia
Arora, Mallika
Adult-Onset Unilateral Disabling Pansclerotic Morphea
title Adult-Onset Unilateral Disabling Pansclerotic Morphea
title_full Adult-Onset Unilateral Disabling Pansclerotic Morphea
title_fullStr Adult-Onset Unilateral Disabling Pansclerotic Morphea
title_full_unstemmed Adult-Onset Unilateral Disabling Pansclerotic Morphea
title_short Adult-Onset Unilateral Disabling Pansclerotic Morphea
title_sort adult-onset unilateral disabling pansclerotic morphea
topic E-Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037973/
https://www.ncbi.nlm.nih.gov/pubmed/24891683
http://dx.doi.org/10.4103/0019-5154.131459
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