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伴有空泡化2型纤维局灶性颗粒变性改变的远端肌病。

Distal myopathy with focal granular degenerative change in vacuolated type 2 fibers.

作者信息

Swash M, Schwarz M S, Thompson A, Cox E, Gray A

机构信息

Department of Neurology, London Hospital, UK.

出版信息

Clin Neuropathol. 1988 Sep-Oct;7(5):249-53.

PMID:3208463
Abstract

A slowly progressive distal myopathy with raised blood (CK) level commencing in the second decade was associated with large vacuoles found only in type 2 fibers. The vacuoles consisted of sarcoplasmic spaces without limiting membranes, containing granular and fibrillar material. This material probably represented degenerative products derived from myofibrils. A distinction is drawn between these degenerative vacuolar changes and those reported in other cases of sporadic or hereditary distal myopathy in which autophagic vacuoles are characteristic.

摘要

一种始于第二个十年、血肌酸激酶(CK)水平升高的缓慢进行性远端肌病与仅在2型纤维中发现的大空泡有关。这些空泡由无界膜的肌浆间隙组成,含有颗粒状和纤维状物质。这种物质可能代表源自肌原纤维的退化产物。这些退化性空泡变化与散发性或遗传性远端肌病其他病例中报道的变化有所不同,后者以自噬空泡为特征。

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