Schuborg C, Mertens F, Rydholm A, Brosjö O, Dictor M, Mitelman F, Mandahl N
Department of Clinical Genetics, Lund University Hospital, Sweden.
Cancer Genet Cytogenet. 1998 Jan 1;100(1):52-6. doi: 10.1016/s0165-4608(97)00012-5.
Angiosarcomas are rare malignant vascular tumors, most commonly found in the skin or superficial soft tissue. We found clonal chromosome aberrations in four short-term cultured angiosarcomas. Two cases were diagnosed as epithelioid angiosarcomas, and one as postmastectomy angiosarcoma. Two of the tumors were deep-seated and two were superficial. Angiosarcomas from deep, soft tissue are extremely rare and have never been cytogenetically investigated before. The chromosome number ranged from hypodiploid to hypertriploid. When the results from the present study were combined with data on the four previously reported cytogenetically aberrant angiosarcomas, the most frequently rearranged chromosomes were 5, 7, 8, 13, 15, 20, 22, and the Y chromosome. Recurrent changes, each found in three of these eight angiosarcomas, were gains of 5pter-p11, 8p12-qter, and 20pter-q12, losses of 7pter-p15 and 22q13-qter, and -Y in two of three men.
血管肉瘤是罕见的恶性血管肿瘤,最常见于皮肤或浅表软组织。我们在4例短期培养的血管肉瘤中发现了克隆性染色体畸变。2例被诊断为上皮样血管肉瘤,1例为乳房切除术后血管肉瘤。其中2例肿瘤位于深部,2例位于浅表。深部软组织血管肉瘤极为罕见,此前从未进行过细胞遗传学研究。染色体数目从亚二倍体到超三倍体不等。当本研究结果与之前报道的4例细胞遗传学异常的血管肉瘤数据相结合时,最常发生重排的染色体是5、7、8、13、15、20、22和Y染色体。在这8例血管肉瘤中的3例中均发现的反复出现的变化包括5pter-p11、8p12-qter和20pter-q12的增加,7pter-p15和22q13-qter的缺失,以及3名男性中有2名出现-Y。