A Case of Progressive Ossifying Fibrodysplasia of Tracheobronchial Respiratory Muscles.

Case Reports in Radiology Pub Date : 2019-02-11 eCollection Date: 2019-01-01 DOI:10.1155/2019/5095343
Nouraly Habib, Anhum Konan, Tra Bi Zamble Olivier Didier
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引用次数: 1

Abstract

The authors report a case of progressive ossifying myositis (POM) in a 13-year-old boy, revealed by dry cough and dyspnea. Conventional chest x-rays and whole-body CT showed extraskeletal ossification that seems to affect the left bronchial strain and trachea. This lesional topography, if established, not yet described to our knowledge, contrasts with the observations of all the authors, including Munchmeyer, for whom smooth muscles and muscles attached to the skeleton by a single end are spared by the heterotopic ossifications characteristic of the disease. Therefore, this observation raises the question of the ubiquity of muscle ossifications during POM.

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气管支气管呼吸肌进行性骨化性纤维发育不良1例。
作者报告一例进行性骨化性肌炎(POM)在一个13岁的男孩,表现为干咳和呼吸困难。常规胸部x光片和全身CT显示骨骼外骨化,似乎影响了左支气管劳损和气管。这种病变地形,如果确定,但据我们所知尚未描述,与包括Munchmeyer在内的所有作者的观察结果形成对比,对他来说,平滑肌和通过单端附着在骨骼上的肌肉没有受到疾病特征异位骨化的影响。因此,这一观察结果提出了POM期间肌肉骨化普遍存在的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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