血友病的矫形手术。

Q3 Medicine
Anna Rosa Rizzo, Manuel Zago, Christian Carulli, Massimo Innocenti
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引用次数: 8

摘要

血友病现在可能被认为是一种“矫形儿科”疾病,因为几乎所有血友病患者都涉及肌肉骨骼系统。现代血液学预防大大提高了生活质量,减少了出血和危及生命的并发症;然而,关节出血、进行性和不可逆性关节病变和骨质疏松症仍然是目前常见的挑战问题。血友病涉及的组织之一是骨骼,特别是在关节周围区:骨质质量差和骨储备减少是典型的模式,关节病变越严重,骨质流失越大。这种情况的骨科管理现在是强制性的,并以几种外科技术为特征。这项工作的目的是从我们管理血友病患者的经验中提供这些选择的概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orthopaedic procedures in haemophilia.

Haemophilia may nowadays be considered an "ortho paedic" disease given due to the involvement of musculoskeletal system in almost all haemophilic subjects. The modern haematological prophylaxis has dramatically improved the quality of life reducing bleedings and life-threatening complications; however, joint bleedings, progressive and irreversible arthropathy and osteoporosis are still now common challenging issues to be faced. One of the tissues involved by Haemophilia is the bone, particularly in the periarticular zone: poor bone quality and decrease of bone stock are typical patterns, and the worse is the arthropathy, the greater the bone loss. The orthopaedic management of such condition is now mandatory and characterized by several surgical techniques. The purpose of this work is to provide an overview of these options derived from our experience in managing haemophilic patients.

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来源期刊
Clinical Cases in Mineral and Bone Metabolism
Clinical Cases in Mineral and Bone Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
2.60
自引率
0.00%
发文量
0
期刊介绍: The Journal encourages the submission of case reports and clinical vignettes that provide new and exciting insights into the pathophysiology and characteristics of disorders related to skeletal function and mineral metabolism and/or highlight pratical diagnostic and /or therapeutic considerations.
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