Carter R L, Jameson C F, Philp E R, Pinkerton C R
Institute of Cancer Research, Royal Marsden Hospital, Sutton, Surrey, UK.
Histopathology. 1990 Oct;17(4):301-9. doi: 10.1111/j.1365-2559.1990.tb00733.x.
The morphological and immunohistochemical phenotypes of 51 rhabdomyosarcomas from young people have been described and contrasted with phenotypes in developing skeletal muscle from 20 fetuses and neonates. The tumours express markers in a cumulative and consistent sequence--vimentin, desmin, fast myosin, myoglobin--which evolves pari passu with morphological differentiation and follows the same pattern found in normal myogenesis. Changes in immunohistochemical phenotype are documented in residual and recurrent tumours excised after chemotherapy. The presumptive rhabdomyoblastic nature of some primitive tumours, marking with vimentin alone, is discussed.
本文描述了51例青少年横纹肌肉瘤的形态学和免疫组织化学表型,并将其与20例胎儿和新生儿发育中的骨骼肌表型进行对比。肿瘤以累积且一致的顺序表达标志物——波形蛋白、结蛋白、快肌球蛋白、肌红蛋白——这一顺序与形态学分化同步发展,且与正常肌生成过程中发现的模式相同。化疗后切除的残留和复发性肿瘤的免疫组织化学表型变化也有记录。文中还讨论了一些仅以波形蛋白标记的原始肿瘤的推定横纹肌母细胞性质。