Clinical characteristics of hereditary multiple exostoses: a retrospective study of mainland chinese cases in recent 23 years.
10.1007/s11596-014-1230-3
- Author:
Xue-ling GUO
1
;
Yan DENG
;
Hui-guo LIU
Author Information
1. Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Key Laboratory of Respiratory Disease of the Ministry of Health, Wuhan, 430030, China, guoxueling0301@hotmail.com.
- Publication Type:Journal Article
- MeSH:
Adult;
Asian Continental Ancestry Group;
genetics;
Cell Transformation, Neoplastic;
genetics;
China;
epidemiology;
Exostoses, Multiple Hereditary;
diagnosis;
ethnology;
genetics;
Family Health;
Female;
Genetic Predisposition to Disease;
genetics;
Humans;
Male;
Membrane Proteins;
genetics;
Middle Aged;
Mutation;
N-Acetylglucosaminyltransferases;
genetics;
Polymorphism, Genetic;
Prevalence;
Retrospective Studies;
Sex Factors;
Tumor Suppressor Proteins;
genetics;
Young Adult
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2014;34(1):42-50
- CountryChina
- Language:English
-
Abstract:
Hereditary multiple exostoses (HME) are an autosomal dominant skeletal disease with wide variations in clinical manifestations among different ethnic groups. This study investigated the epidemiology, clinical presentations, pathogenetic features and treatment strategies of HME in mainland China. We searched and reviewed the related cases published since 1990 by searching electronic databases, namely SinoMed database, Wanfang database, CNKI, Web of Science and PubMed as well as Google search engines. A total of 1051 cases of HME (male-to-female ratio 1.5:1) were investigated and the diagnosis was made in 83% before the age of 10 years. Approximately 96% patients had a family history. Long bones, ribs, scapula and pelvis were the frequently affected sites. Most patients were asymptomatic with multiple palpable masses. Common complications included angular deformities, impingement on neighbouring tissues and impaired articular function. Chondrosarcomas transformation occurred in 2% Chinese cases. Among the cases examined, about 18% had mutations in EXT1 and 28% in EXT2. Frameshift, nonsense and missense mutations represented the majority of HME-causing mutations. Diagnosis of HME was made based on the clinical presentations and radiological documentations. Most patients needed no treatment. Surgical treatment was often directed to remove symptomatic exostoses, particularly those of suspected malignancy degeneration, and correction of skeletal deformities. This study shows some variance from current literature regarding other ethnic populations and may provide valuable baseline assessment of the natural history of HME in mainland China.
