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Femoral head osteochondritis dissecans in a child

This case report describes an early-adolescent boy with an osteochondritis dissecans (OCD) lesion of the left femoral head secondary to significant acetabular dysplasia and coxa valga of the proximal femur. Patient underwent left proximal femur varus osteotomy. Follow-up imaging demonstrates healing...

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Autores principales: Hernandez, Sean G, McQueen, Ryan G, Erickson, John B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030482/
https://www.ncbi.nlm.nih.gov/pubmed/36931689
http://dx.doi.org/10.1136/bcr-2022-253375
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author Hernandez, Sean G
McQueen, Ryan G
Erickson, John B
author_facet Hernandez, Sean G
McQueen, Ryan G
Erickson, John B
author_sort Hernandez, Sean G
collection PubMed
description This case report describes an early-adolescent boy with an osteochondritis dissecans (OCD) lesion of the left femoral head secondary to significant acetabular dysplasia and coxa valga of the proximal femur. Patient underwent left proximal femur varus osteotomy. Follow-up imaging demonstrates healing and resolution of the OCD lesion. Future plan for left hip is periacetabular osteotomy, following triradiate cartilage closure, to correct acetabular dysplasia. The aim of this case report is to support clinicians in the assessment and treatment of this rare condition.
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spelling pubmed-100304822023-03-23 Femoral head osteochondritis dissecans in a child Hernandez, Sean G McQueen, Ryan G Erickson, John B BMJ Case Rep Case Reports: Rare disease This case report describes an early-adolescent boy with an osteochondritis dissecans (OCD) lesion of the left femoral head secondary to significant acetabular dysplasia and coxa valga of the proximal femur. Patient underwent left proximal femur varus osteotomy. Follow-up imaging demonstrates healing and resolution of the OCD lesion. Future plan for left hip is periacetabular osteotomy, following triradiate cartilage closure, to correct acetabular dysplasia. The aim of this case report is to support clinicians in the assessment and treatment of this rare condition. BMJ Publishing Group 2023-03-17 /pmc/articles/PMC10030482/ /pubmed/36931689 http://dx.doi.org/10.1136/bcr-2022-253375 Text en © BMJ Publishing Group Limited 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Case Reports: Rare disease
Hernandez, Sean G
McQueen, Ryan G
Erickson, John B
Femoral head osteochondritis dissecans in a child
title Femoral head osteochondritis dissecans in a child
title_full Femoral head osteochondritis dissecans in a child
title_fullStr Femoral head osteochondritis dissecans in a child
title_full_unstemmed Femoral head osteochondritis dissecans in a child
title_short Femoral head osteochondritis dissecans in a child
title_sort femoral head osteochondritis dissecans in a child
topic Case Reports: Rare disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030482/
https://www.ncbi.nlm.nih.gov/pubmed/36931689
http://dx.doi.org/10.1136/bcr-2022-253375
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