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骨髓增生异常综合征的临床病理谱及新型核型发现:印度三级医疗中心的经验

Clinico-Pathological Spectrum and Novel Karyotypic Findings in Myelodysplastic Syndrome: Experience of Tertiary Care Center in India.

作者信息

Gupta Ruchi, Rahman Khaliqur, Singh Manish Kumar, Kumari Surabhi, Yadav Geeta, Nityanand Soniya

机构信息

Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.

出版信息

Mediterr J Hematol Infect Dis. 2017 Aug 16;9(1):e2017048. doi: 10.4084/MJHID.2017.048. eCollection 2017.

Abstract

BACKGROUND

Myelodysplastic syndrome (MDS) is a heterogeneous disorder characterized clinically by the presence of cytopenia/s. Limited data are available about the morphological spectrum and cytogenetic profile of Indian MDS patients. The aim of the study was to ascertain the clinico-pathological, morphological and cytogenetic spectrum of Indian MDS patients.

MATERIAL AND METHODS

A retrospective analysis of all patients diagnosed with MDS from June 2012 to December 2016 was performed. Their clinical and laboratory data were collated and reviewed.

RESULTS

A total of 150 patients with primary MDS were evaluated with M: F ratio of 1.6:1 and the median age of 55.5 years. 64% patients presented with pancytopenia and 31% with bicytopenia. Morphologically they included MDS-MLD [63 (42%)], MDS-EB 2, [33 (22%)], MDS-EB 1 [32 (21.3%)], MDS-SLD [13 (8.6%)] and two cases (1.4%) each of MDS-SLD-RS, MDS-MLD-RS, and RCC. An abnormal cytogenetic profile was detected in 50% patients. Complex karyotype was observed to be the commonest abnormality (32.5%), and chromosome 7 was the most frequently involved chromosome. Isolated deletion 5q was seen in 6.9 % cases. Novel translocations like t(9;22)(q11.2;q34.2), t(1;5)(p22;q33), t(1;12)(p34;p11.2) and t(5;7;9)(q13;q32;p22) were observed in addition to other complex abnormalities. The majority of the patients belonged to the high risk IPSS-R prognostic groups (31.4%); followed by intermediate and very high-risk groups, 29% and 24.4% respectively.

CONCLUSION

The median age of patients in India is a decade younger than the western population. Complex karyotype was observed to be the commonest cytogenetic abnormality, while the frequency of deletion 5q and trisomy 8 was much lower as compared to the west. The majority of the patients were in high to very high IPSS-R risk categories and seventy percent individuals below 40 years showed abnormal karyotype, indicating that Indian MDS patients have high disease burden at a young age and thus more likelihood for leukemic transformation.

摘要

背景

骨髓增生异常综合征(MDS)是一种异质性疾病,临床特征为血细胞减少。关于印度MDS患者的形态学谱和细胞遗传学特征的数据有限。本研究的目的是确定印度MDS患者的临床病理、形态学和细胞遗传学谱。

材料与方法

对2012年6月至2016年12月期间所有诊断为MDS的患者进行回顾性分析。整理并回顾他们的临床和实验室数据。

结果

共评估了150例原发性MDS患者,男女比例为1.6:1,中位年龄为55.5岁。64%的患者表现为全血细胞减少,31%表现为两系血细胞减少。形态学上,他们包括MDS-MLD[63例(42%)]、MDS-EB 2[33例(22%)]、MDS-EB 1[32例(21.3%)]、MDS-SLD[13例(8.6%)],以及各2例(1.4%)的MDS-SLD-RS、MDS-MLD-RS和RCC。50%的患者检测到异常细胞遗传学特征。复杂核型被观察到是最常见的异常(32.5%),7号染色体是最常受累的染色体。6.9%的病例可见孤立的5q缺失。除其他复杂异常外,还观察到新的易位,如t(9;22)(q11.2;q34.2)、t(1;5)(p22;q33)、t(1;12)(p34;p11.2)和t(5;7;9)(q13;q32;p22)。大多数患者属于高风险IPSS-R预后组(31.4%);其次是中危和极高危组,分别为29%和24.4%。

结论

印度患者的中位年龄比西方人群小十岁。复杂核型被观察到是最常见的细胞遗传学异常,而5q缺失和8三体的频率与西方相比要低得多。大多数患者处于高至极高的IPSS-R风险类别,40岁以下的个体中有70%显示核型异常,这表明印度MDS患者在年轻时疾病负担较高,因此白血病转化的可能性更大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e0b/5584769/6ffbeec50bed/mjhid-9-1-e2017048f1.jpg

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