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Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report

INTRODUCTION: Osteochondrosis of humeral capitellum (Panner’s disease) is a rare condition. Very few cases are reported in the literature and may be overlooked or misdiagnosed. Most cases are unilateral in distribution and occur in young boys during the first decade of life. It is often difficult to...

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Autores principales: Chavda, Sumant, Abeid, Khaled Abou, Alhajri, Khawla Khaled, Hasan, Noora Husain Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576768/
https://www.ncbi.nlm.nih.gov/pubmed/34790609
http://dx.doi.org/10.13107/jocr.2021.v11.i07.2324
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author Chavda, Sumant
Abeid, Khaled Abou
Alhajri, Khawla Khaled
Hasan, Noora Husain Ali
author_facet Chavda, Sumant
Abeid, Khaled Abou
Alhajri, Khawla Khaled
Hasan, Noora Husain Ali
author_sort Chavda, Sumant
collection PubMed
description INTRODUCTION: Osteochondrosis of humeral capitellum (Panner’s disease) is a rare condition. Very few cases are reported in the literature and may be overlooked or misdiagnosed. Most cases are unilateral in distribution and occur in young boys during the first decade of life. It is often difficult to distinguish osteochondrosis from osteochondritis dissecans of the humeral capitellum that occurs in older children and adolescents in the second decade of life. CASE REPORT: We describe a case of a 6-year-old boy who presented with pain, subtle swelling and limited extension in his right elbow following a fall. Diagnosis of Panner’s disease was made 2 weeks later on follow-up based on classical features on plain radiograph of joint effusion, irregular delineation of the articular contour, and faint sclerosis of the capitellum with a radiolucent line in the subchondral bone. The patient had uneventful full functional recovery with conservative treatment: Rest, temporary immobilization, and subsequent remobilization. CONCLUSION: Osteochondrosis of humeral capitellum though rare is a known condition. It may be overlooked or misdiagnosed. High degree of awareness is required and diagnosis can be made with utmost care based on the age of presentation, clinical signs and clearly recognizable plain radiographic features of joint effusion, irregular articular outline with radiolucent line in subchondral bone and faint sclerosis of capitellum.
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spelling pubmed-85767682021-11-16 Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report Chavda, Sumant Abeid, Khaled Abou Alhajri, Khawla Khaled Hasan, Noora Husain Ali J Orthop Case Rep Case Report INTRODUCTION: Osteochondrosis of humeral capitellum (Panner’s disease) is a rare condition. Very few cases are reported in the literature and may be overlooked or misdiagnosed. Most cases are unilateral in distribution and occur in young boys during the first decade of life. It is often difficult to distinguish osteochondrosis from osteochondritis dissecans of the humeral capitellum that occurs in older children and adolescents in the second decade of life. CASE REPORT: We describe a case of a 6-year-old boy who presented with pain, subtle swelling and limited extension in his right elbow following a fall. Diagnosis of Panner’s disease was made 2 weeks later on follow-up based on classical features on plain radiograph of joint effusion, irregular delineation of the articular contour, and faint sclerosis of the capitellum with a radiolucent line in the subchondral bone. The patient had uneventful full functional recovery with conservative treatment: Rest, temporary immobilization, and subsequent remobilization. CONCLUSION: Osteochondrosis of humeral capitellum though rare is a known condition. It may be overlooked or misdiagnosed. High degree of awareness is required and diagnosis can be made with utmost care based on the age of presentation, clinical signs and clearly recognizable plain radiographic features of joint effusion, irregular articular outline with radiolucent line in subchondral bone and faint sclerosis of capitellum. Indian Orthopaedic Research Group 2021-07 2021-07 /pmc/articles/PMC8576768/ /pubmed/34790609 http://dx.doi.org/10.13107/jocr.2021.v11.i07.2324 Text en Copyright: © Indian Orthopaedic Research Group https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under 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
Chavda, Sumant
Abeid, Khaled Abou
Alhajri, Khawla Khaled
Hasan, Noora Husain Ali
Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title_full Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title_fullStr Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title_full_unstemmed Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title_short Osteochondrosis of Humeral Capitellum, Diagnosis and Treatment – A Case Report
title_sort osteochondrosis of humeral capitellum, diagnosis and treatment – a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576768/
https://www.ncbi.nlm.nih.gov/pubmed/34790609
http://dx.doi.org/10.13107/jocr.2021.v11.i07.2324
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