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骨巨细胞型恶性纤维组织细胞瘤的肿瘤进展:临床、放射学、组织学及细胞遗传学证据

Tumor progression in a giant cell type malignant fibrous histiocytoma of bone: clinical, radiologic, histologic, and cytogenetic evidence.

作者信息

Molenaar W M, van den Berg E, Veth R P, Dijkhuizen T, de Vries E G

机构信息

Department of Pathology, University Hospital of Groningen, The Netherlands.

出版信息

Genes Chromosomes Cancer. 1994 May;10(1):66-70. doi: 10.1002/gcc.2870100111.

Abstract

A malignant fibrous histiocytoma (MFH) of bone arising in the fibula of a 21-year-old woman is described. Clinical, radiologic, and histologic findings demonstrated rapid tumor progression. Chromosomal analysis of the biopsy specimen showed great karyotypic heterogeneity, whereas the resection specimen four weeks later displayed a rather homogeneous karyotype. Both revealed a clonal t(14;22)(q11;p12). Several other clonal and non-clonal chromosomal aberrations were observed. Some of these were previously described in giant cell tumor of bone (GCTB) and may correlate with aggressive behavior, e.g., aberrations involving 8p11, 19q13, and 20q13. The change from karyotypic heterogeneity to relative homogeneity may be related to tumor progression. The chromosomal findings further suggest that the giant cell type of MFH of bone may be related to malignant GCTB.

摘要

本文描述了一名21岁女性腓骨发生的骨恶性纤维组织细胞瘤(MFH)。临床、放射学和组织学检查结果显示肿瘤进展迅速。活检标本的染色体分析显示核型高度异质性,而四周后的切除标本显示核型较为均一。两者均显示克隆性t(14;22)(q11;p12)。还观察到其他一些克隆性和非克隆性染色体畸变。其中一些先前在骨巨细胞瘤(GCTB)中已有描述,可能与侵袭性行为相关,例如涉及8p11、19q13和20q13的畸变。从核型异质性到相对均一性的变化可能与肿瘤进展有关。染色体检查结果进一步提示骨MFH的巨细胞型可能与恶性GCTB相关。

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