Whang-Peng J, Triche T J, Knutsen T, Miser J, Kao-Shan S, Tsai S, Israel M A
Cancer Genet Cytogenet. 1986 Apr 1;21(3):185-208. doi: 10.1016/0165-4608(86)90001-4.
Small, round, blue-cell tumors (SRCT), including rhabdomyosarcoma, Ewing's sarcoma of bone and soft tissue, mesenchymal chondrosarcoma, small cell osteosarcoma, hemangiopericytoma, neuroblastoma, peripheral neurectodermal tumor (peripheral neuroepithelioma of bone and soft tissue), and the malignant small cell tumor of the thoracopulmonary region described by Askin (Askin's tumor), are often difficult to distinguish by light microscopy. We have evaluated the cytogenetics of these tumors by studying 24 tumor explants in short-term culture and 22 tumor cell lines. In Ewing's sarcoma (a tumor of unknown histogenesis), and in peripheral neuroepithelioma and Askin's tumor (tumors with evidence of neural origin), we have observed an indistinguishable t(11;22) translocation.
小圆蓝细胞肿瘤(SRCT),包括横纹肌肉瘤、骨与软组织的尤因肉瘤、间叶性软骨肉瘤、小细胞骨肉瘤、血管外皮细胞瘤、神经母细胞瘤、外周神经外胚层肿瘤(骨与软组织的外周神经上皮瘤)以及阿斯金描述的胸肺区域恶性小细胞肿瘤(阿斯金瘤),通常通过光学显微镜检查难以区分。我们通过研究24个短期培养的肿瘤外植体和22个肿瘤细胞系,评估了这些肿瘤的细胞遗传学。在尤因肉瘤(一种组织发生不明的肿瘤)、外周神经上皮瘤和阿斯金瘤(有神经起源证据的肿瘤)中,我们观察到了无法区分的t(11;22)易位。