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一名后来发展为中央核性肌病的患者体内有大量微小肌管。

Abundant minute myotubes in a patient who later developed centronuclear myopathy.

作者信息

Wöckel L, Ketelsen U P, Stötter M, Laule S, Meyermann R, Bornemann A

机构信息

Institute of Brain Research, University of Tübingen, Germany.

出版信息

Acta Neuropathol. 1998 May;95(5):547-51. doi: 10.1007/s004010050836.

Abstract

Centronuclear myopathy (CNM) is a congenital myopathy which manifests itself as a severe neonatal (also termed myotubular myopathy), early-onset, or adult form. The histological pattern of each is marked by a considerable number of nuclei of muscle fibers being internally placed. Owing to their remote resemblance to myotubes, and their expression of developmentally regulated proteins, most authors now favor the concept that myogenesis is arrested or delayed in this disease. We here present two muscle biopsy specimens of a patient with early-onset CNM, taken at the age of 5 months and 14 years, respectively. The first biopsy sample contained internally placed nuclei in 7% of the muscle fibers, abundant minute myotubes, and hypertrophic muscle fibers. The second biopsy sample showed internally placed nuclei in 40% of the muscle fibers, and hypotrophic fibers. We suggest that the histological findings in early-onset CNM are the result of a complex dynamic process, which includes a delay in maturation.

摘要

中央核肌病(CNM)是一种先天性肌病,表现为严重的新生儿型(也称为肌管性肌病)、早发型或成人型。每种类型的组织学模式的特征是大量肌纤维核位于内部。由于它们与肌管有一定的相似性,且表达发育调控蛋白,现在大多数作者倾向于认为在这种疾病中肌生成停滞或延迟。我们在此展示了一名早发型CNM患者的两份肌肉活检标本,分别取自5个月和14岁时。第一份活检样本中,7%的肌纤维有内部核,有丰富的微小肌管和肥大的肌纤维。第二份活检样本显示40%的肌纤维有内部核,以及萎缩的纤维。我们认为早发型CNM的组织学发现是一个复杂动态过程的结果,其中包括成熟延迟。

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