Trisomy 3 in gastric lymphomas of extranodal marginal zone B-cell (mucosa-associated lymphoid tissue) origin demonstrated by FISH in intact paraffin tissue sections

被引:26
作者
Blanco, R
Lyda, M
Davis, B
Kraus, M
Fenoglio-Preiser, C
机构
[1] Univ Cincinnati, Coll Med, Cincinnati, OH USA
[2] Washington Univ, Sch Med, Barnes Hosp, St Louis, MO USA
关键词
extranodal marginal zone B-cell lymphoma (MZBCL); mucosa-associated lymphoid tissue (MALT); non-Hodgkin's lymphoma (NHL); low-grade B-cell lymphoma (LGBCL); large cell lymphoma (LCL); trisomy; human chromosomes; pair; 3; interphase cytogenetics; fluorescence in situ hybridization (FISH);
D O I
10.1016/S0046-8177(99)90098-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Some reports have indicated that trisomy 3 represents a characteristic chromosomal abnormality found in lymphomas arising in mucosa-associated lymphoid tissues (MALT)/extranodal marginal zone B-cells (MZBC). Traditional cytogenetic analysis of metaphase preparations is cumbersome and not always possible, especially in those situations in which the diagnosis in not suspected before a biopsy. Our aim is to use a relatively simple method to evaluate trisomy 3 in paraffin-embedded, formalin-fixed tissue, using fluorescence in situ hybridization (FISH) on intact tissue sections. Formalin-fixed, paraffin-embedded archival tissues from 30 cases (27 lymphoma and 3 chronic gastritis cases) were hybridized with a chromosome 3 specific alpha-satellite probe (ONCOR, Gaithersburg, MD). Three of four cases of gastric MZBC/MALT lymphoma revealed trisomy 3. Ten cases of lymphoma of possible or probable MZBC origin were examined, and four revealed trisomy 3. Five of 13 non-MZBC lymphomas revealed trisomy 3. None of the chronic gastritis cases nor normal tonsil cases revealed trisomy 3. Our results, using a different methodological approach, confirm the findings of others that trisomy 3 is an abnormality found in a significant proportion of lymphomas of MZBC origin. Our approach also makes possible interphase cytogenetic analysis (by FISH) of routinely processed formalin-fixed, paraffin-embedded tissues, without the need to disaggregate cells. It thus may facilitate genetic analysis on specimens previously deemed unsuitable for such analysis, particularly when tissue quantity is limited. Copyright (C) 1999 by W.B. Saunders Company.
引用
收藏
页码:706 / 711
页数:6
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