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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Indian Orthopaedic Research Group
2021
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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. |
format | Online Article Text |
id | pubmed-8576768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Indian Orthopaedic Research Group |
record_format | MEDLINE/PubMed |
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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