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Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis

We report a novel case of a pediatric patient with bilateral hip destruction from untreated Juvenile idiopathic arthritis (JIA). She was presented at the age of 9 with hip pain associated with bilateral acetabular dysplasia and a dislocated left femoral head. Only 1.5 years later, the patient develo...

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Detalles Bibliográficos
Autores principales: Calafi, Arash, Skaggs, Alton W., Shelton, Trevor J., Haus, Brian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431357/
https://www.ncbi.nlm.nih.gov/pubmed/30963013
http://dx.doi.org/10.1155/2019/4593129
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author Calafi, Arash
Skaggs, Alton W.
Shelton, Trevor J.
Haus, Brian M.
author_facet Calafi, Arash
Skaggs, Alton W.
Shelton, Trevor J.
Haus, Brian M.
author_sort Calafi, Arash
collection PubMed
description We report a novel case of a pediatric patient with bilateral hip destruction from untreated Juvenile idiopathic arthritis (JIA). She was presented at the age of 9 with hip pain associated with bilateral acetabular dysplasia and a dislocated left femoral head. Only 1.5 years later, the patient developed complete destruction of the left femoral head and dislocated right femoral head. The authors have not identified literature describing a similar case report of bilateral femoral head destruction resulting from Persistent Oligoarticular JIA. Pediatric patients presenting with rapidly evolving destructive process should be evaluated for rheumatologic, infectious, and spinal etiologies.
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spelling pubmed-64313572019-04-08 Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis Calafi, Arash Skaggs, Alton W. Shelton, Trevor J. Haus, Brian M. Case Rep Orthop Case Report We report a novel case of a pediatric patient with bilateral hip destruction from untreated Juvenile idiopathic arthritis (JIA). She was presented at the age of 9 with hip pain associated with bilateral acetabular dysplasia and a dislocated left femoral head. Only 1.5 years later, the patient developed complete destruction of the left femoral head and dislocated right femoral head. The authors have not identified literature describing a similar case report of bilateral femoral head destruction resulting from Persistent Oligoarticular JIA. Pediatric patients presenting with rapidly evolving destructive process should be evaluated for rheumatologic, infectious, and spinal etiologies. Hindawi 2019-03-06 /pmc/articles/PMC6431357/ /pubmed/30963013 http://dx.doi.org/10.1155/2019/4593129 Text en Copyright © 2019 Arash Calafi et al. http://creativecommons.org/licenses/by/4.0/ 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
Calafi, Arash
Skaggs, Alton W.
Shelton, Trevor J.
Haus, Brian M.
Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title_full Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title_fullStr Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title_full_unstemmed Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title_short Bilateral Destructive Hip Disease from Untreated Juvenile Idiopathic Arthritis
title_sort bilateral destructive hip disease from untreated juvenile idiopathic arthritis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431357/
https://www.ncbi.nlm.nih.gov/pubmed/30963013
http://dx.doi.org/10.1155/2019/4593129
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