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Developmental pattern of the hip in patients with hereditary multiple exostoses
BACKGROUND: Coxa valga is a common clinical feature of hereditary multiple exostoses (HME). The current study aimed to determine the unique developmental pattern of the hip in patients with HME and evaluate the factors that influence its progression. METHODS: Thirty patients (57 hips) with HME were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429362/ https://www.ncbi.nlm.nih.gov/pubmed/25888017 http://dx.doi.org/10.1186/s12891-015-0514-5 |
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author | Wang, Ya-Zhou Park, Kwang-Won Oh, Chang-Seon Ahn, Yeong-Seub Kang, Qing-Lin Jung, Sung-Taek Song, Hae-Ryong |
author_facet | Wang, Ya-Zhou Park, Kwang-Won Oh, Chang-Seon Ahn, Yeong-Seub Kang, Qing-Lin Jung, Sung-Taek Song, Hae-Ryong |
author_sort | Wang, Ya-Zhou |
collection | PubMed |
description | BACKGROUND: Coxa valga is a common clinical feature of hereditary multiple exostoses (HME). The current study aimed to determine the unique developmental pattern of the hip in patients with HME and evaluate the factors that influence its progression. METHODS: Thirty patients (57 hips) with HME were divided into two groups according to the Hilgenreiner epiphyseal angle (HEA). Twenty-two patients (44 hips) including 13 men and 9 women were assigned to group 1 (HEA <25°), and 8 patients (13 hips) including 3 men and 5 women were assigned to group 2 (HEA ≥25°). The mean age at the initial presentation was 6.0 (4–12) years with 6.8 (4–11) years of follow-up in group 1, and 10.4 (8–13) years with 5.4 (2–9) years of follow-up in group 2. We measured the HEA, neck-shaft angle (NSA), acetabular index (AI), center-edge angle (CEA), and migration percentage (MP) for radiographic evaluation. RESULTS: Among the hips, 50 (87.7%) hips had coxa valga and 27 (47.4%) hips had abnormal MP (42.1% were borderline and 5.3% were subluxated). There was a significant difference in the HEA and NSA between the groups (p < 0.001 and p < 0.05, respectively). The HEA significantly correlated with the development of the NSA and no correlation was found between the HEA and AI, CEA, and MP. CONCLUSIONS: There was a significant relationship between the HEA at the initial presentation and the NSA at skeletal maturity. We should consider guided growth for patients with lower HEA to prevent significant coxa valga deformity with close follow-up. |
format | Online Article Text |
id | pubmed-4429362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44293622015-05-14 Developmental pattern of the hip in patients with hereditary multiple exostoses Wang, Ya-Zhou Park, Kwang-Won Oh, Chang-Seon Ahn, Yeong-Seub Kang, Qing-Lin Jung, Sung-Taek Song, Hae-Ryong BMC Musculoskelet Disord Research Article BACKGROUND: Coxa valga is a common clinical feature of hereditary multiple exostoses (HME). The current study aimed to determine the unique developmental pattern of the hip in patients with HME and evaluate the factors that influence its progression. METHODS: Thirty patients (57 hips) with HME were divided into two groups according to the Hilgenreiner epiphyseal angle (HEA). Twenty-two patients (44 hips) including 13 men and 9 women were assigned to group 1 (HEA <25°), and 8 patients (13 hips) including 3 men and 5 women were assigned to group 2 (HEA ≥25°). The mean age at the initial presentation was 6.0 (4–12) years with 6.8 (4–11) years of follow-up in group 1, and 10.4 (8–13) years with 5.4 (2–9) years of follow-up in group 2. We measured the HEA, neck-shaft angle (NSA), acetabular index (AI), center-edge angle (CEA), and migration percentage (MP) for radiographic evaluation. RESULTS: Among the hips, 50 (87.7%) hips had coxa valga and 27 (47.4%) hips had abnormal MP (42.1% were borderline and 5.3% were subluxated). There was a significant difference in the HEA and NSA between the groups (p < 0.001 and p < 0.05, respectively). The HEA significantly correlated with the development of the NSA and no correlation was found between the HEA and AI, CEA, and MP. CONCLUSIONS: There was a significant relationship between the HEA at the initial presentation and the NSA at skeletal maturity. We should consider guided growth for patients with lower HEA to prevent significant coxa valga deformity with close follow-up. BioMed Central 2015-03-15 /pmc/articles/PMC4429362/ /pubmed/25888017 http://dx.doi.org/10.1186/s12891-015-0514-5 Text en © Wang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Article Wang, Ya-Zhou Park, Kwang-Won Oh, Chang-Seon Ahn, Yeong-Seub Kang, Qing-Lin Jung, Sung-Taek Song, Hae-Ryong Developmental pattern of the hip in patients with hereditary multiple exostoses |
title | Developmental pattern of the hip in patients with hereditary multiple exostoses |
title_full | Developmental pattern of the hip in patients with hereditary multiple exostoses |
title_fullStr | Developmental pattern of the hip in patients with hereditary multiple exostoses |
title_full_unstemmed | Developmental pattern of the hip in patients with hereditary multiple exostoses |
title_short | Developmental pattern of the hip in patients with hereditary multiple exostoses |
title_sort | developmental pattern of the hip in patients with hereditary multiple exostoses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429362/ https://www.ncbi.nlm.nih.gov/pubmed/25888017 http://dx.doi.org/10.1186/s12891-015-0514-5 |
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