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皮肤良性纤维组织细胞瘤克隆性的细胞遗传学证据:CHAMP研究组报告

Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group.

作者信息

Vanni R, Fletcher C D, Sciot R, Dal Cin P, De Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Tallini G, Van Den Berghe H, Willén H

机构信息

Department of Applied Sciences Biosystems, University of Cagliari, Italy.

出版信息

Histopathology. 2000 Sep;37(3):212-7. doi: 10.1046/j.1365-2559.2000.00947.x.

Abstract

AIMS

Cutaneous benign fibrohistiocytic tumours are among the most common soft tissue lesions. Their biological nature, in particular whether they are neoplastic or reactive, has long been disputed. Some morphological subtypes can be confused with sarcoma. Since available karyotypic data in these lesions are scarce, this study was undertaken to determine whether their cytogenetic analysis might demonstrate clonality and might help in differential diagnosis.

METHODS AND RESULTS

Thirteen karyotyped benign cutaneous fibrous histiocytomas (BFH) were morphologically reassessed and classified as ordinary BFH (eight cases), cellular BFH (four cases), and one ankle-type lesion. Five cases (38%) showed clonal cytogenetic changes, although the aberrations varied and did not correlate with histological subtypes. Karyotypic aberrations were more common in cellular BFH (3/4) than in the ordinary BFH (2/8).

CONCLUSIONS

The demonstration of clonal chromosome abnormalities, in at least some cases, supports the neoplastic nature of cutaneous BFH. The karyotypic changes identified are different from those in dermatofibrosarcoma, with which cellular BFH is often confused histologically.

摘要

目的

皮肤良性纤维组织细胞瘤是最常见的软组织病变之一。其生物学性质,尤其是它们是肿瘤性还是反应性的,长期以来一直存在争议。一些形态学亚型可能会与肉瘤混淆。由于这些病变中可用的核型数据稀缺,因此开展本研究以确定其细胞遗传学分析是否可能显示克隆性并有助于鉴别诊断。

方法与结果

对13例进行了核型分析的皮肤良性纤维组织细胞瘤(BFH)进行形态学重新评估,并分类为普通BFH(8例)、细胞性BFH(4例)和1例踝部型病变。5例(38%)显示出克隆性细胞遗传学改变,尽管畸变各不相同且与组织学亚型无关。细胞性BFH(3/4)中的核型畸变比普通BFH(2/8)更常见。

结论

至少在某些病例中克隆染色体异常的显示支持皮肤BFH的肿瘤性质。所确定的核型变化不同于皮肤纤维肉瘤中的变化,细胞性BFH在组织学上常与皮肤纤维肉瘤混淆。

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