Suppr超能文献

婴儿组织细胞样心肌病:一种原因不明的肌纤维变性。

Histiocytoid cardiomyopathy of infancy: an unexplained myofibre degeneration.

作者信息

Bruton D, Herdson P B, Becroft D M

出版信息

Pathology. 1977 Apr;9(2):115-22. doi: 10.3109/00313027709085249.

Abstract

An unusual multifocal degeneration of the myofibres of all chambers and the conducting system of the heart was found in a 4-month-old female in whom ventricular pre-excitation (Wolff-Parkinson-White syndrome) had been demonstrated. There was a complex malformation of the brain with hydrocephalus and bilateral corneal opacities and microphthalmos. The affected myofibres had a swollen vacuolated or granular cytoplasm and rounded nuclei giving a histiocytoid appearance. Disruption of myofibrils and gross dilation and disorganization of mitochondria were the major fine structural features. Reports of similar lesions in 8 other young female children are reviewed. 'Histiocytoid cardiomyopathy' is the term preferred over others which refer to an increased lipid content. The aetiology is unknown.

摘要

在一名4个月大的女性患儿中发现了心脏所有腔室及传导系统肌纤维的一种罕见的多灶性变性,该患儿已被证实存在心室预激( Wolff-Parkinson-White综合征)。患儿还伴有复杂的脑部畸形,包括脑积水、双侧角膜混浊和小眼畸形。受影响的肌纤维细胞质肿胀,呈空泡状或颗粒状,细胞核圆形,呈现组织细胞样外观。肌原纤维破坏以及线粒体明显扩张和结构紊乱是主要的超微结构特征。本文回顾了其他8例年轻女童类似病变的报告。相较于其他提及脂质含量增加的术语,“组织细胞样心肌病”是更为合适的称呼。病因不明。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验