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Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review

BACKGROUND: Slipped capital femoral epiphysis (SCFE) is a common hip disorder characterized by displacement of the capital femoral epiphysis from the metaphysic through the femoral epiphyseal plate. SCFE usually occurs during puberty, with obesity a common risk factor. We experienced a rare case of...

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Autores principales: Kadowaki, Saori, Hori, Tomohiro, Matsumoto, Hideki, Kanda, Kaori, Ozeki, Michio, Shirakami, Yu, Kawamoto, Norio, Ohnishi, Hidenori, Fukao, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604342/
https://www.ncbi.nlm.nih.gov/pubmed/28923047
http://dx.doi.org/10.1186/s12902-017-0210-6
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author Kadowaki, Saori
Hori, Tomohiro
Matsumoto, Hideki
Kanda, Kaori
Ozeki, Michio
Shirakami, Yu
Kawamoto, Norio
Ohnishi, Hidenori
Fukao, Toshiyuki
author_facet Kadowaki, Saori
Hori, Tomohiro
Matsumoto, Hideki
Kanda, Kaori
Ozeki, Michio
Shirakami, Yu
Kawamoto, Norio
Ohnishi, Hidenori
Fukao, Toshiyuki
author_sort Kadowaki, Saori
collection PubMed
description BACKGROUND: Slipped capital femoral epiphysis (SCFE) is a common hip disorder characterized by displacement of the capital femoral epiphysis from the metaphysic through the femoral epiphyseal plate. SCFE usually occurs during puberty, with obesity a common risk factor. We experienced a rare case of SCFE associated with hypothyroidism in a prepubescent patient who was not obese. CASE PRESENTATION: The patient was an 8-year-old boy suffering from bilateral SCFE with hypothyroidism. The patient’s growth had started to slow at 4 years of age, and at 8 years he was of short stature. During his evaluation for SCFE management, primary hypothyroidism was diagnosed due to the presence of anti-thyroid peroxidase and anti-thyroglobulin antibodies. After the patient was treated for hypothyroidism, which improved his thyroid function, surgery was performed for bilateral SCFE. CONCLUSIONS: Among the 42 patients with SCFE associated with hypothyroidism in the literature, most SCFE occurred during puberty or in adults with delayed epiphyseal closure. Only two patients (4.8%), including the present patient, were ≤9 years old. Although being overweight or obese is common for patients with SCFE associated with hypothyroidism (76.0%), it was not observed in the present case. Persistent hypothyroidism, however, may be a risk factor for SCFE even before puberty and without obesity.
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spelling pubmed-56043422017-09-21 Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review Kadowaki, Saori Hori, Tomohiro Matsumoto, Hideki Kanda, Kaori Ozeki, Michio Shirakami, Yu Kawamoto, Norio Ohnishi, Hidenori Fukao, Toshiyuki BMC Endocr Disord Case Report BACKGROUND: Slipped capital femoral epiphysis (SCFE) is a common hip disorder characterized by displacement of the capital femoral epiphysis from the metaphysic through the femoral epiphyseal plate. SCFE usually occurs during puberty, with obesity a common risk factor. We experienced a rare case of SCFE associated with hypothyroidism in a prepubescent patient who was not obese. CASE PRESENTATION: The patient was an 8-year-old boy suffering from bilateral SCFE with hypothyroidism. The patient’s growth had started to slow at 4 years of age, and at 8 years he was of short stature. During his evaluation for SCFE management, primary hypothyroidism was diagnosed due to the presence of anti-thyroid peroxidase and anti-thyroglobulin antibodies. After the patient was treated for hypothyroidism, which improved his thyroid function, surgery was performed for bilateral SCFE. CONCLUSIONS: Among the 42 patients with SCFE associated with hypothyroidism in the literature, most SCFE occurred during puberty or in adults with delayed epiphyseal closure. Only two patients (4.8%), including the present patient, were ≤9 years old. Although being overweight or obese is common for patients with SCFE associated with hypothyroidism (76.0%), it was not observed in the present case. Persistent hypothyroidism, however, may be a risk factor for SCFE even before puberty and without obesity. BioMed Central 2017-09-18 /pmc/articles/PMC5604342/ /pubmed/28923047 http://dx.doi.org/10.1186/s12902-017-0210-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Kadowaki, Saori
Hori, Tomohiro
Matsumoto, Hideki
Kanda, Kaori
Ozeki, Michio
Shirakami, Yu
Kawamoto, Norio
Ohnishi, Hidenori
Fukao, Toshiyuki
Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title_full Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title_fullStr Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title_full_unstemmed Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title_short Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
title_sort prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604342/
https://www.ncbi.nlm.nih.gov/pubmed/28923047
http://dx.doi.org/10.1186/s12902-017-0210-6
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