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恶性纤维组织细胞瘤的细胞遗传学研究

A cytogenetic study of malignant fibrous histiocytoma.

作者信息

Szymanska J, Tarkkanen M, Wiklund T, Virolainen M, Blomqvist C, Asko-Seljavaara S, Tukiainen E, Elomaa I, Knuutila S

机构信息

Department of Medical Genetics, University of Helsinki, Finland.

出版信息

Cancer Genet Cytogenet. 1995 Dec;85(2):91-6. doi: 10.1016/0165-4608(95)00143-3.

Abstract

We report the results of cytogenetic analysis of malignant fibrous histiocytoma of soft tissue (MFH). Seven of 12 successfully cultured MFHs had complex clonal aberrations, including translocations, deletions, and unidentifiable marker chromosomes. Telomeric associations were observed in five and the double minute phenomenon in four of seven MFHs with abnormal karyotypes. In one case (a storiform-pleomorphic MFH, grade IV) with a complex polyploid karyotype, two clonal ring chromosomes were present, one interpreted as r(19)(p13q13), one unidentified. In two tumors, clonal structural rearrangements of chromosome 1 were seen: del(1)(q21) in a storiform-pleomorphic MFH, grade IV, and add (1)(q21 or q32), t(1;10)(p22;q22) in a myxoid MFH, grade I. The remaining five MFHs had normal karyotypes, but in two of them nonclonal, structural aberrations were found. The modal chromosome number in the studied MFHs varied widely, but the majority of tumors with abnormal karyotypes had polyploid chromosome complements (five of seven cases). Our results confirm many of the previous findings and indicate that double minutes (dmins) may be more frequent in MFH than previously reported.

摘要

我们报告了软组织恶性纤维组织细胞瘤(MFH)的细胞遗传学分析结果。12例成功培养的MFH中,7例存在复杂的克隆性畸变,包括易位、缺失和无法识别的标记染色体。在7例核型异常的MFH中,5例观察到端粒联合,4例出现双微体现象。在1例(1例四级的席纹状多形性MFH)具有复杂多倍体核型的病例中,存在两条克隆性环状染色体,一条被解释为r(19)(p13q13),另一条无法识别。在2例肿瘤中,可见1号染色体的克隆性结构重排:1例四级的席纹状多形性MFH中为del(1)(q21),1例一级的黏液样MFH中为add(1)(q21或q32)、t(1;10)(p22;q22)。其余5例MFH核型正常,但其中2例发现非克隆性结构畸变。所研究的MFH的众数染色体数目差异很大,但大多数核型异常的肿瘤具有多倍体染色体组成(7例中有5例)。我们的结果证实了许多先前的发现,并表明双微体(dmins)在MFH中可能比先前报道的更为常见。

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