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11号染色体长臂1区3带缺失作为髓系恶性肿瘤的唯一异常:4例新病例及简要综述

Deletion (11)(q13) as the sole anomaly in myeloid malignancies: four new cases and a short review.

作者信息

Panani Anna D, Pappa Vasiliki, Papageorgiou Sotirios, Stamatelli Francs, Raptis Sotirios A

机构信息

Second Department of Internal Medicine Propaedeutic, Research Unit of Athens University, Evangelismos Hospital, 10676, Athens, Greece.

出版信息

Ann Hematol. 2004 Mar;83(3):153-5. doi: 10.1007/s00277-003-0823-x. Epub 2003 Dec 10.

Abstract

Chromosomal abnormalities are of significance in the study of hematologic malignancies. We describe one case of myelodysplastic syndrome (MDS) diagnosed 22 years ago as polycythemia vera (PV) as well as a case of unclassified myeloproliferative disease (MPD) with a poor clinical course. Both patients presented del(11)(q13) as the sole clonal abnormality. This abnormality was also found in two additional cases of MDS. Summarizing the literature, only ten other cases of myeloid malignancies with deletion of 11q involving band q13 as the sole anomaly have been reported. All but one of these cases presented interstitial deletions.

摘要

染色体异常在血液系统恶性肿瘤的研究中具有重要意义。我们描述了一例22年前被诊断为真性红细胞增多症(PV)的骨髓增生异常综合征(MDS)病例,以及一例临床病程较差的未分类骨髓增殖性疾病(MPD)病例。两名患者均表现为del(11)(q13)作为唯一的克隆性异常。在另外两例MDS病例中也发现了这种异常。总结文献,仅另有十例髓系恶性肿瘤报告其11q缺失累及q13带作为唯一异常。这些病例中除一例之外均表现为间质缺失。

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