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作 者:Jens Krugmann Alexandar Tzankov Stephan Dirnhofer Falko Fend Dominik Wolf Reiner Siebert Pensiri Probst Martin Erdel
机构地区:[1]Institute of PathologyMedical University of Innsbruck,Austria Department of Medical Genetics,Molecular and Clinical Pharmacology,Medical University of Innsbruck,Austria [2]Institute of PathologyMedical University of Innsbruck,Austria [3]Institute of PathologyUniversity of Basel,Switzerland [4]Institute of PathologyTechnical University of Munich,Germany [5]Department of Internal MedicineDivision of Hematology/Oncology,Medical University of Innsbruck,Austria [6]Institute of Human GeneticsUniversity Hospital Schleswig-Holstein Campus Kiel,Germany [7]Department of Medical GeneticsMolecular and Clinical Pharmacology,Medical University of Innsbruck,Austria
出 处:《World Journal of Gastroenterology》2005年第46期7384-7385,共2页世界胃肠病学杂志(英文版)
摘 要:Taji et al . have reported in their study on 13 patients with gastric mucosa-associated lymphoid tissue (MALT) lymphomas an aggressive tumor course in trisomy 3 positive cases. The authors analyzed only stage I patients with classical low-grade marginal zone lymphoma of the MALT type and detected the trisomy 3 using an alphasatellite DNA probe directed to the centromere. Their data support the observation that trisomy 3 is the most frequent cytogenetic aberration in MALT lymphomas .TO THE EDITORTaji et al.[1] have reported in their study on 13 patients with gastric mucosa-associated lymphoid tissue (MALT) lymphomas an aggressive tumor course in trisomy 3 positive cases. The authors analyzed only stage I patients with classical low-grade marginal zone lymphoma of the MALT type and detected the trisomy 3 using an alphasatellite DNA probe directed to the centromere. Their data support the observation that trisomy 3 is the most frequent cytogenetic aberration in MALT lymphomas[2,3].
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