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[胎儿横纹肌瘤。病例报告及超微结构研究]

[Foetal Rhabdomyoma. Case report and ultrastructural study].

作者信息

Walter P, Guerbaoui M

出版信息

Virchows Arch A Pathol Anat Histol. 1976 Aug 19;371(1):59-67. doi: 10.1007/BF00433715.

Abstract

Benign voluntary muscle tumours are exceedingly rare. Only 9 fetal and 35 adult type rhabdomyomata have been reported in the literature, former usually in children, the latter in adults. Both types affect the musculature of the head and neck almost exclusively. In this ultrastructural study of a fetal rhabdomyoma in a girl aged eleven years, we have found that the tumour is composed of cells showing myoblastic or myotubular differentiation although the myofilaments are poorly arranged and the myofibrils irregularly distributed. Motor-end plates have not been observed. These observations, together with the light microscopic findings and a review of previously described cellular characteristics, suggest that fetal and adult rhabdomyoma are different stages in the life history of the same tumour. Whether the lesion should be considered to be a hamartoma or a neoplasm is uncertain.

摘要

良性自愿性肌肉肿瘤极为罕见。文献中仅报道过9例胎儿型和35例成人型横纹肌瘤,前者多见于儿童,后者多见于成人。这两种类型几乎都仅累及头颈部肌肉组织。在对一名11岁女孩的胎儿型横纹肌瘤进行的超微结构研究中,我们发现肿瘤由显示成肌细胞或肌管分化的细胞组成,尽管肌丝排列不佳且肌原纤维分布不规则。未观察到运动终板。这些观察结果,连同光镜检查结果以及对先前描述的细胞特征的回顾,表明胎儿型和成人型横纹肌瘤是同一肿瘤生命历程中的不同阶段。该病变应被视为错构瘤还是肿瘤尚不确定。

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