Sciot R, Rosai J, Dal Cin P, de Wever I, Fletcher C D, Mandahl N, Mertens F, Mitelman F, Rydholm A, Tallini G, van den Berghe H, Vanni R, Willén H
Department of Pathology, University of Leuven, Belgium.
Mod Pathol. 1999 Jun;12(6):576-9.
The karyotypes of 44 specimens from 35 patients with localized (n = 19) or diffuse (n = 16) tenosynovial giant cell tumors were studied. The majority of cases in both categories (11 of 19 localized; 12 of 16 diffuse) displayed clonal chromosomal aberrations, with a complex karyotype in three cases and a simple chromosomal aberration in the others. No difference in the distribution of karyotypic abnormalities was found between the localized and diffuse form except for trisomies (usually of chromosomes 5 and/or 7), which were more frequent in the diffuse type. The short arm of chromosome 1 (1p11-13) was most frequently rearranged, with 7 of 11 localized and 7 of 12 diffuse lesions affected. These findings indicate that the localized and diffuse forms of tenosynovial giant cell tumor might represent two morphologic manifestations of the same entity. The high frequency of clonal chromosomal abnormalities, with a clustering of structural rearrangements to 1p11-13, suggests that this disease is most likely neoplastic in nature and paves the way to search for gene(s) that might be involved in its development.
对35例局限性(n = 19)或弥漫性(n = 16)腱鞘巨细胞瘤患者的44份标本进行了核型研究。两类病例中的大多数(19例局限性中的11例;16例弥漫性中的12例)显示出克隆性染色体畸变,其中3例为复杂核型,其他为简单染色体畸变。除三体性(通常为5号和/或7号染色体)外,局限性和弥漫性形式在核型异常分布上未发现差异,三体性在弥漫型中更常见。1号染色体短臂(1p11 - 13)最常发生重排,11例局限性病变中有7例、12例弥漫性病变中有7例受累。这些发现表明,腱鞘巨细胞瘤的局限性和弥漫性形式可能代表同一实体的两种形态学表现。克隆性染色体异常的高频率以及结构重排聚集在1p11 - 13,提示该疾病很可能本质上是肿瘤性的,并为寻找可能参与其发生发展的基因铺平了道路。