Two novel translocations, t(2;4)(q35;q31) and t(X;12)(q22;q24), as the only karyotypic abnormalities in a malignant peripheral nerve sheath tumor of the skull base

被引:10
作者
Gil, Z
Fliss, DA [1 ]
Voskoboimik, N
Trejo-Leider, L
Khafif, A
Yaron, Y
Orr-Urtreger, A
机构
[1] Tel Aviv Univ, Dept Otolaryngol Head & Neck Surg, Skull Base Surg Unit, Tel Aviv, Israel
[2] Tel Aviv Univ, Inst Genet, Tel Aviv, Israel
[3] Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, Tel Aviv, Israel
关键词
D O I
10.1016/S0165-4608(03)00036-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant peripheral nerve sheath tumor (MPNST) is a rare neoplasm that originates from Schwann cells and comprises 5%-10% of soft tissue sarcomas. Cytogenetic analysis of this tumor has shown a highly complex karyotype, and no single chromosomal aberration has been reported to date. We combined spectral karyotyping analysis and G-banding for cytogenetic characterization of this unique tumor, which originated in the anterior skull base. We report the simultaneous occurrence of a t(2;4)(q35;q31) and a t(X;12)(q22;q24) as the only chromosomal abnormalities in this tumor. To the best of our knowledge, apparently balanced translocations have not been identified previously in MPNST. (C) 2003 Elsevier Inc. All rights reserved.
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页码:139 / 143
页数:5
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