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成人T细胞急性淋巴细胞淋巴瘤合并髓系肉瘤:一例报告

T cell acute lymphoblastic lymphoma complicated with myeloid sarcoma in an adult: A case report.

作者信息

Wang Ying, Wen Shupeng, Niu Zhiyun, Xing Lina, Wang Fuxu, Zhang Xuejun

机构信息

Department of Hematology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei 050000, P.R. China.

出版信息

Oncol Lett. 2017 Dec;14(6):8178-8182. doi: 10.3892/ol.2017.7187. Epub 2017 Oct 16.

Abstract

The present case report describes a rare case of T cell acute lymphoblastic lymphoma (T-LBL) in the lymph node with myeloid sarcoma in the pericardium. A 33-year-old Chinese male was admitted to hospital on 4 July 2015 exhibiting a fever and having experienced wheezing and fatigue for the previous 7 days. Routine pathological, computed tomographic, cytological and immunophenotypic observations revealed a diagnosis of T-LBL in the lymph node on 7 August 2015, without evidence of bone marrow (BM) involvement. The patient received induction chemotherapy for T-LBL and achieved partial remission. The patient was identified to have multiple serous effusion and analysis of pericardial effusion cells revealed the diagnosis of T-LBL with extramedullary myeloid sarcoma (without BM involvement) on 25 November 2015. On 30 December 2015, the patient was identified to exhibit proliferation of primary myeloid cells in the peripheral blood and BM, and an abnormal karyotype in BM cells, indicating that the complicated myeloid sarcoma involved the BM. No matched donor was available so the patient received chemotherapy to manage the disease. The patient was discharged on 31 January 2016 and ceased treatment. The patient succumbed on 19 February 2016 at home. To the best of our knowledge, T-LBL complicated with myeloid sarcoma had not been previously reported in Chinese adult male patients. In addition, the involvement of the BM and aberrant karyotype of the complicated myeloid sarcoma in the patient were rare.

摘要

本病例报告描述了一例罕见的淋巴结T细胞急性淋巴细胞白血病(T-LBL)合并心包髓系肉瘤的病例。一名33岁中国男性于2015年7月4日入院,此前7天出现发热、喘息和疲劳症状。常规病理、计算机断层扫描、细胞学和免疫表型观察显示,2015年8月7日诊断为淋巴结T-LBL,无骨髓(BM)受累证据。该患者接受了T-LBL诱导化疗并达到部分缓解。2015年11月25日,患者被发现有多处浆液性积液,心包积液细胞分析显示诊断为T-LBL合并髓外髓系肉瘤(无BM受累)。2015年12月30日,患者被发现外周血和BM中原始髓系细胞增殖,BM细胞核型异常,表明复杂的髓系肉瘤累及BM。由于没有匹配的供体,患者接受了化疗来控制病情。患者于2016年1月31日出院并停止治疗。患者于2016年2月19日在家中死亡。据我们所知,T-LBL合并髓系肉瘤此前在中国成年男性患者中未见报道。此外,该患者复杂髓系肉瘤累及BM及异常核型的情况罕见。

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