Frugoni (Verona) P, Ferlito (Padua) A
J Laryngol Otol. 1976 Jul;90(7):687-98. doi: 10.1017/s0022215100082578.
A case of pleomorphic rhabdomyosarcoma of the larynx occurring in a 33-year-old male is reported. The clinical and histopathological aspects of this undoubtedly rare neoplasm are described. After a quick review of the most important classifications of rhabdomyosarcoma so far made, the authors suggest a division into two basic groups, i.e. pleomorphic and fetal rhabdomyosarcoma, while the botryoid sarcoma and the alveolar rhabdomyosarcoma should be considered only as two subgroups of fetal rhabdomyosarcoma. From a comprehensive review of world literature on the subject, the well-documented cases up to now described are only seven, including the authors. The present case is the third one after the instances of pleomorphic rhabdomyosarcoma reported by Filipo and Crifo (1964 and by Rodriquez and Ziskind (1970).
报告了一例发生在一名33岁男性身上的喉多形性横纹肌肉瘤。描述了这种无疑罕见的肿瘤的临床和组织病理学特征。在快速回顾了迄今为止最重要的横纹肌肉瘤分类后，作者建议将其分为两个基本组，即多形性横纹肌肉瘤和胎儿型横纹肌肉瘤，而葡萄状肉瘤和肺泡状横纹肌肉瘤应仅被视为胎儿型横纹肌肉瘤的两个亚组。从对该主题的世界文献的全面回顾来看，迄今为止有充分记录的病例（包括作者的病例在内）只有7例。本病例是继菲利波和克里福（1964年）以及罗德里克斯和齐斯金德（1970年）报告的多形性横纹肌肉瘤病例之后的第三例。
