t(1;6)(p12;p11.1)、5q缺失和环11在1型骨髓增生异常综合征患者中的一例

Anna Okabe, David Palencia, David Shabsovich, Alberto Duarte, Angelica Lopez, Carlos A Tirado
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引用次数: 0

摘要

目的:我们报告一例56岁男性骨髓增生异常综合征(MDS),其骨髓免疫表型显示CD45低阳性和CD34阳性;8.66%的人群MPO、CD16、CD117、CD36、CD33和CD71部分阳性,CD13、HLA-DR和CD11b部分阳性。CD13与CD16、CD13与CD11b的成熟模式未见改变。对成熟淋巴细胞群体的分析显示,87.5%的细胞中CD45高CD3+, 7.6%的细胞中CD45高CD19+, 4.9%的NK细胞。这些结果与骨髓增生异常综合征与1型细胞过量一致。骨髓染色体分析显示,20例中期细胞中有12例出现t(1;6)(p12;p11.1)、缺失5q和环11的异常核型。尚未报道t(1;6)(p12;p11.1)与任何特定的血液学恶性肿瘤相关,这为MDS细胞遗传学异常的范围提供了进一步的见解。
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A Case of t(1;6)(p12;p11.1), Deletion 5q, and Ring 11 in a Patient with Myelodysplastic Syndrome with Excess Blasts Type 1.

Objectives: We present the case of a 56-year-old male with myelodysplastic syndrome (MDS) whose bone marrow immunophenotype showed lower positivity for CD45 and positivity for CD34; 8.66% of this population also expressed partial positives for MPO, CD16, CD117, CD36, CD33, and CD71, as well as positives for CD13, HLA-DR, and CD11b. No alterations in the pattern of maturation were seen in CD13 vs CD16 and CD13 vs CD11b. An analysis of a population of mature lymphocytes revealed CD45 high CD3+ in 87.5% of cells, CD45 high CD19+ in 7.6% of cells, and 4.9% NK cells. These results are consistent with a myelodysplastic syndrome with an excess of blasts type 1. Chromosome analysis of the bone marrow revealed an abnormal karyotype with a t(1;6)(p12;p11.1) as well as deletion 5q and a ring 11 in 12 of the 20 metaphase cells examined. The t(1;6)(p12;p11.1) has not been reported in association with any particular hematological malignancy and provides further insight into the range of cytogenetic abnormalities in MDS.

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