Walter T A, Weh H J, Schlag P M, Zornig C, Hossfeld D K
Universitätskrankenhaus Eppendorf, Abt. Onkologie/Hämatologie, Hamburg, Germany.
Cancer Genet Cytogenet. 1997 Apr;94(2):131-4. doi: 10.1016/s0165-4608(96)00220-8.
Among soft tissue sarcomas, malignant fibrous histiocytoma is considered to be the most commonly encountered tumor-type of late adult life. Cytogenetic data are, however, sparse and contradictory, without any specific anomalies. We are describing the results of cytogenetic studies in 20 malignant fibrous histiocytomas of various subtypes and gradings. Although we saw two single and therefore possibly primary rearrangements, t(13;14) and t(5;7), most tumors had complex rearrangements without sharing any characteristic aberrations. In our opinion, the heterogeneity of these findings supports the concept that malignant fibrous histiocytoma is not a distinctive entity but merely a name for a group of as yet poorly defined sarcomas.
在软组织肉瘤中,恶性纤维组织细胞瘤被认为是成年晚期最常见的肿瘤类型。然而,细胞遗传学数据稀少且相互矛盾,没有任何特定的异常情况。我们正在描述对20例不同亚型和分级的恶性纤维组织细胞瘤进行细胞遗传学研究的结果。虽然我们发现了两个单一的、因此可能是原发性的重排,即t(13;14)和t(5;7),但大多数肿瘤都有复杂的重排,且没有共同的特征性畸变。我们认为,这些发现的异质性支持了这样一种观点,即恶性纤维组织细胞瘤不是一个独特的实体,而仅仅是一组定义尚不明确的肉瘤的名称。