Chromosomal anomalies in a case of proliferative myositis

被引：20

作者：

McComb, EN

Neff, JR

Johansson, SL

Nelson, M

Bridge, JA

机构：

[1] UNIV NEBRASKA,MED CTR,DEPT ORTHOPAED SURG,OMAHA,NE 68198

[2] UNIV NEBRASKA,MED CTR,DEPT PATHOL & MICROBIOL,OMAHA,NE 68198

[3] UNIV NEBRASKA,MED CTR,DEPT PEDIAT,OMAHA,NE 68198

来源：

CANCER GENETICS AND CYTOGENETICS | 1997年 / 98卷 / 02期

关键词：

D O I：

10.1016/S0165-4608(96)00428-1

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Proliferative myositis, a reactive lesion similar to proliferative fasciitis and nodular fasciitis, has only been cytogenetically described in one other report to date. This previously described case showed trisomy 2, Cytogenetic analysis and fluorescence in situ hybridization (FISH) of a proliferative myositis lesion in the present study did not reveal trisomy 2 but the following clonal translocation was observed: 46,XX,t(6;14)(q23;q32). (C) Elsevier Science Inc., 1997.

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收藏

页码：142 / 144

页数：3

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