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Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report

The aim of reporting this case is to highlight the association of two disorders, primary hyperparathyroidism (PHPT) and slipped capital femoral epiphysis (SCFE). They are usually seen in two different age groups and rarely together. PHPT is a rare cause of SCFE and only 10 cases have been reported i...

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Detalles Bibliográficos
Autores principales: Alghamdi, Anas A., Ahmad, Maswood M., Almalki, Mussa H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123767/
https://www.ncbi.nlm.nih.gov/pubmed/27920593
http://dx.doi.org/10.4137/CMED.S40895
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author Alghamdi, Anas A.
Ahmad, Maswood M.
Almalki, Mussa H.
author_facet Alghamdi, Anas A.
Ahmad, Maswood M.
Almalki, Mussa H.
author_sort Alghamdi, Anas A.
collection PubMed
description The aim of reporting this case is to highlight the association of two disorders, primary hyperparathyroidism (PHPT) and slipped capital femoral epiphysis (SCFE). They are usually seen in two different age groups and rarely together. PHPT is a rare cause of SCFE and only 10 cases have been reported in the literature worldwide. The patient in our report is a 13-year-old girl who presented to our clinic with bilateral knee pain and a waddling gait. Subsequent investigations showed that she had PHPT and SCFE with low bone mass. On admission, a parathyroidectomy was performed; then, the slipped femoral epiphyses were fixed with satisfactory results. A systematic algorithmic approach that was illustrated in a previously published case was used. Such cases should be managed with a systematic approach based on the patient’s clinical status to prevent future morbidity. A literature review was conducted by performing a Medline search of all reported cases of PHPT and SCFEs.
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spelling pubmed-51237672016-12-05 Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report Alghamdi, Anas A. Ahmad, Maswood M. Almalki, Mussa H. Clin Med Insights Endocrinol Diabetes Case Report The aim of reporting this case is to highlight the association of two disorders, primary hyperparathyroidism (PHPT) and slipped capital femoral epiphysis (SCFE). They are usually seen in two different age groups and rarely together. PHPT is a rare cause of SCFE and only 10 cases have been reported in the literature worldwide. The patient in our report is a 13-year-old girl who presented to our clinic with bilateral knee pain and a waddling gait. Subsequent investigations showed that she had PHPT and SCFE with low bone mass. On admission, a parathyroidectomy was performed; then, the slipped femoral epiphyses were fixed with satisfactory results. A systematic algorithmic approach that was illustrated in a previously published case was used. Such cases should be managed with a systematic approach based on the patient’s clinical status to prevent future morbidity. A literature review was conducted by performing a Medline search of all reported cases of PHPT and SCFEs. Libertas Academica 2016-11-23 /pmc/articles/PMC5123767/ /pubmed/27920593 http://dx.doi.org/10.4137/CMED.S40895 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Case Report
Alghamdi, Anas A.
Ahmad, Maswood M.
Almalki, Mussa H.
Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title_full Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title_fullStr Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title_full_unstemmed Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title_short Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
title_sort slipped capital femoral epiphysis and primary hyperparathyroidism: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123767/
https://www.ncbi.nlm.nih.gov/pubmed/27920593
http://dx.doi.org/10.4137/CMED.S40895
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