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Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess

Osteomyelitis of the pubis symphysis is a rare condition. There have been various reports in the literature of inflammation and osteomyelitis as well as septic arthritis of pubic symphysis. However, due to the fact that these conditions are rare and that the usual presenting symptoms are very nonspe...

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Autores principales: Alqahtani, Saad M., Jiang, Fan, Barimani, Bardia, Gdalevitch, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279146/
https://www.ncbi.nlm.nih.gov/pubmed/25580335
http://dx.doi.org/10.1155/2014/982171
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author Alqahtani, Saad M.
Jiang, Fan
Barimani, Bardia
Gdalevitch, Marie
author_facet Alqahtani, Saad M.
Jiang, Fan
Barimani, Bardia
Gdalevitch, Marie
author_sort Alqahtani, Saad M.
collection PubMed
description Osteomyelitis of the pubis symphysis is a rare condition. There have been various reports in the literature of inflammation and osteomyelitis as well as septic arthritis of pubic symphysis. However, due to the fact that these conditions are rare and that the usual presenting symptoms are very nonspecific, osteomyelitis of the pubic symphysis is often misdiagnosed, thus delaying definitive treatment. We present a case that to our knowledge is the first case in literature of osteomyelitis of the pubic symphysis in a 17-year-old boy with juvenile idiopathic arthritis (JIA), which was initially misdiagnosed and progressed to bilateral adductor abscesses. A high suspicion of such condition should be considered in a JIA patient who presents with symphysis or thigh pain.
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spelling pubmed-42791462015-01-11 Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess Alqahtani, Saad M. Jiang, Fan Barimani, Bardia Gdalevitch, Marie Case Rep Orthop Case Report Osteomyelitis of the pubis symphysis is a rare condition. There have been various reports in the literature of inflammation and osteomyelitis as well as septic arthritis of pubic symphysis. However, due to the fact that these conditions are rare and that the usual presenting symptoms are very nonspecific, osteomyelitis of the pubic symphysis is often misdiagnosed, thus delaying definitive treatment. We present a case that to our knowledge is the first case in literature of osteomyelitis of the pubic symphysis in a 17-year-old boy with juvenile idiopathic arthritis (JIA), which was initially misdiagnosed and progressed to bilateral adductor abscesses. A high suspicion of such condition should be considered in a JIA patient who presents with symphysis or thigh pain. Hindawi Publishing Corporation 2014 2014-12-14 /pmc/articles/PMC4279146/ /pubmed/25580335 http://dx.doi.org/10.1155/2014/982171 Text en Copyright © 2014 Saad M. Alqahtani et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Alqahtani, Saad M.
Jiang, Fan
Barimani, Bardia
Gdalevitch, Marie
Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title_full Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title_fullStr Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title_full_unstemmed Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title_short Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess
title_sort symphysis pubis osteomyelitis with bilateral adductor muscles abscess
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279146/
https://www.ncbi.nlm.nih.gov/pubmed/25580335
http://dx.doi.org/10.1155/2014/982171
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