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Pachydermodactyly – A Case Report and Review of Literature

INTRODUCTION: Pachydermodactyly is an uncommon or under diagnosed variant of digital fibromatosis. It is a benign disease, described by symmetric proximal interphalangeal (PIP) involvement, progressive swelling, absence of inflammation or pain, and without limitation of function. It has been linked...

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Autores principales: Saidy, Elias, Maalouly, Joseph, Darwish, Mohammad, Cortbawi, Chawki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276560/
https://www.ncbi.nlm.nih.gov/pubmed/32547987
http://dx.doi.org/10.13107/jocr.2020.v10.i01.1650
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author Saidy, Elias
Maalouly, Joseph
Darwish, Mohammad
Cortbawi, Chawki
author_facet Saidy, Elias
Maalouly, Joseph
Darwish, Mohammad
Cortbawi, Chawki
author_sort Saidy, Elias
collection PubMed
description INTRODUCTION: Pachydermodactyly is an uncommon or under diagnosed variant of digital fibromatosis. It is a benign disease, described by symmetric proximal interphalangeal (PIP) involvement, progressive swelling, absence of inflammation or pain, and without limitation of function. It has been linked in some cases with psychiatric disorders such as obsessive-compulsive disorder or repetitive mechanical stimulation. CASE REPORT: We aim to report a case of pachydermodactyly that was diagnosed in a young 17-year-old male patient with painless swelling of the digits mainly at PIP joints with hyperkeratosis that was treated conservatively. CONCLUSION: Pachydermodactyly is an under diagnosed and underestimated entity; the recognition of a case in clinical practice can prove to be challenging. A high index of suspicion must be kept at all times when no reason for the swelling is found.
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spelling pubmed-72765602020-06-15 Pachydermodactyly – A Case Report and Review of Literature Saidy, Elias Maalouly, Joseph Darwish, Mohammad Cortbawi, Chawki J Orthop Case Rep Case Report INTRODUCTION: Pachydermodactyly is an uncommon or under diagnosed variant of digital fibromatosis. It is a benign disease, described by symmetric proximal interphalangeal (PIP) involvement, progressive swelling, absence of inflammation or pain, and without limitation of function. It has been linked in some cases with psychiatric disorders such as obsessive-compulsive disorder or repetitive mechanical stimulation. CASE REPORT: We aim to report a case of pachydermodactyly that was diagnosed in a young 17-year-old male patient with painless swelling of the digits mainly at PIP joints with hyperkeratosis that was treated conservatively. CONCLUSION: Pachydermodactyly is an under diagnosed and underestimated entity; the recognition of a case in clinical practice can prove to be challenging. A high index of suspicion must be kept at all times when no reason for the swelling is found. Indian Orthopaedic Research Group 2020 /pmc/articles/PMC7276560/ /pubmed/32547987 http://dx.doi.org/10.13107/jocr.2020.v10.i01.1650 Text en Copyright: © Indian Orthopaedic Research Group http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commonsunder 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 Case Report
Saidy, Elias
Maalouly, Joseph
Darwish, Mohammad
Cortbawi, Chawki
Pachydermodactyly – A Case Report and Review of Literature
title Pachydermodactyly – A Case Report and Review of Literature
title_full Pachydermodactyly – A Case Report and Review of Literature
title_fullStr Pachydermodactyly – A Case Report and Review of Literature
title_full_unstemmed Pachydermodactyly – A Case Report and Review of Literature
title_short Pachydermodactyly – A Case Report and Review of Literature
title_sort pachydermodactyly – a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276560/
https://www.ncbi.nlm.nih.gov/pubmed/32547987
http://dx.doi.org/10.13107/jocr.2020.v10.i01.1650
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