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Pachydermoperiostosis Mimicking Acromegaly: A Case Report

Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachyderma, and periosteal hypertrophy. Coarsening of facial features and spade-like enlargement of hands and feet may give rise to a diagnostic dilemma between pachydermoperiostosis and acromegaly. This r...

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Autores principales: Prerna, Ghosh, Romana, Barua, Jayanta K., Das, Arup K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956866/
https://www.ncbi.nlm.nih.gov/pubmed/29854639
http://dx.doi.org/10.4103/idoj.IDOJ_230_17
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author Prerna,
Ghosh, Romana
Barua, Jayanta K.
Das, Arup K.
author_facet Prerna,
Ghosh, Romana
Barua, Jayanta K.
Das, Arup K.
author_sort Prerna,
collection PubMed
description Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachyderma, and periosteal hypertrophy. Coarsening of facial features and spade-like enlargement of hands and feet may give rise to a diagnostic dilemma between pachydermoperiostosis and acromegaly. This report highlights a case of a 36-year-old man who presented with broadening of hands and feet, facial skin thickening, and edematous and drooping eyelids for the last 10 years. There was no history of similar presentation in his family. Such clinical presentation in corroboration with normal growth hormone level and prominent radiological abnormalities prompted us to make a diagnosis of pachydermoperiostosis.
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spelling pubmed-59568662018-05-31 Pachydermoperiostosis Mimicking Acromegaly: A Case Report Prerna, Ghosh, Romana Barua, Jayanta K. Das, Arup K. Indian Dermatol Online J Case Report Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachyderma, and periosteal hypertrophy. Coarsening of facial features and spade-like enlargement of hands and feet may give rise to a diagnostic dilemma between pachydermoperiostosis and acromegaly. This report highlights a case of a 36-year-old man who presented with broadening of hands and feet, facial skin thickening, and edematous and drooping eyelids for the last 10 years. There was no history of similar presentation in his family. Such clinical presentation in corroboration with normal growth hormone level and prominent radiological abnormalities prompted us to make a diagnosis of pachydermoperiostosis. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5956866/ /pubmed/29854639 http://dx.doi.org/10.4103/idoj.IDOJ_230_17 Text en Copyright: © 2018 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Prerna,
Ghosh, Romana
Barua, Jayanta K.
Das, Arup K.
Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title_full Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title_fullStr Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title_full_unstemmed Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title_short Pachydermoperiostosis Mimicking Acromegaly: A Case Report
title_sort pachydermoperiostosis mimicking acromegaly: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956866/
https://www.ncbi.nlm.nih.gov/pubmed/29854639
http://dx.doi.org/10.4103/idoj.IDOJ_230_17
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