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遗传性多发性外生骨疣的一个不寻常病例报告:病例报告及文献复习。

An unusual example of hereditary multiple exostoses: a case report and review of the literature.

机构信息

Human Anatomy Resource Centre, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, L69 3GE, UK.

Department of Musculoskeletal and Ageing Science, Institute of Life Course & Medical Sciences, University of Liverpool, Liverpool, UK.

出版信息

BMC Musculoskelet Disord. 2021 Jan 21;22(1):96. doi: 10.1186/s12891-021-03967-6.

Abstract

BACKGROUND

Hereditary multiple exostoses (HME) is a rare skeletal disorder characterised by a widespread. distribution of osteochondromas originating from the metaphyses of long bones.

CASE PRESENTATION

This case study examines a 55-year-old male cadaver bequeathed to the University of Liverpool who suffered from HME, thus providing an exceptionally rare opportunity to examine the anatomical changes associated with this condition.

CONCLUSIONS

Findings from imaging and dissection indicated that this was a severe case of HME in terms of the quantity and distribution of the osteochondromas and the number of synostoses present. In addition, the existence of enchondromas and the appearance of gaps within the trabeculae of affected bones make this a remarkable case. This study provides a comprehensive overview of the morbidity of the disease as well as adding to the growing evidence that diseases concerning benign cartilaginous tumours may be part of a spectrum rather than distinct entities.

摘要

背景

遗传性多发性外生骨疣(HME)是一种罕见的骨骼疾病,其特征是长骨干骺端广泛分布骨软骨瘤。

病例介绍

本病例研究检查了一具捐赠给利物浦大学的 55 岁男性尸体,该男子患有 HME,因此提供了一个极其罕见的机会来检查与这种疾病相关的解剖变化。

结论

影像学和解剖学结果表明,就骨软骨瘤的数量和分布以及存在的骨融合数量而言,这是一例严重的 HME。此外,软骨瘤的存在以及受影响骨骼的小梁内出现间隙使这成为一个显著的病例。本研究全面概述了疾病的发病率,并增加了越来越多的证据,即涉及良性软骨肿瘤的疾病可能是一个谱系的一部分,而不是不同的实体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5915/7818741/03ee80915ee6/12891_2021_3967_Fig1_HTML.jpg

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