Gonazlez-Crussi F, Black-Schaffer S
Am J Surg Pathol. 1979 Apr;3(2):157-71. doi: 10.1097/00000478-197904000-00008.
The classification of the histologic types of rhabdomyosarcoma is based on poorly defined criteria. This has resulted in marked disparities in studies reported from different institutions, as well as difficulties in assessment of the clinical behavior of the different histologic types. A retrospective morphologic analysis of 36 consecutive cases of rhabdomyosarcoma of childhood was undertaken according to predefined and strict guidelines for diagnosis. Undeflecting adherence to such criteria identified the embryonal type as the most common form, and the alveolar variant as a distinct clinicopathologic entity with a much more aggressive course; it also resulted in a large proportion (approximately one-fourth) of sarcomas of undertermined histogenesis. In spite of either prolonged follow-up observation with repeated biopsies, autopsy study, or electron-microscopic study of tumor tissue, no evidence could be obtained to substantiate the rhabdomyogenic derivation of the latter group of neoplasms. Precise systematization of the morphology of these cases may be contingent upon careful inventory of their fine structural features; current classifications appear to have disregarded the morphologic heterogeneity of this group of tumors.
横纹肌肉瘤组织学类型的分类基于定义不明确的标准。这导致不同机构报告的研究存在显著差异,也给评估不同组织学类型的临床行为带来困难。根据预定义的严格诊断指南,对36例儿童横纹肌肉瘤连续病例进行了回顾性形态学分析。严格遵循这些标准确定胚胎型为最常见的形式,肺泡型变异体为具有更具侵袭性病程的独特临床病理实体;这也导致很大一部分(约四分之一)组织发生不明的肉瘤。尽管对肿瘤组织进行了长期随访观察、重复活检、尸检研究或电子显微镜研究,但仍无法获得证据证实后一组肿瘤的横纹肌源性起源。这些病例形态学的精确系统化可能取决于对其精细结构特征的仔细清查;目前的分类似乎忽视了这组肿瘤的形态学异质性。