Feng Hao, Qiao Jianlin, Ding Ningning, Chen Wei, Qi Kunming, Pan Xiuying, Cao Jiang, Xu Kailin
Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, Jiangsu, China.
Case Rep Hematol. 2016;2016:8261249. doi: 10.1155/2016/8261249. Epub 2016 Sep 25.
We report a case of Sjögren's syndrome (SS) complicated by myeloid/natural killer (NK) cell precursor acute leukemia (M/NKPAL). A 75-year-old woman with a previous SS history for 2 years was routinely treated. Peripheral blood progenitor cells were increased, and subsequent bone marrow cell morphology examination showed the presence of acute myeloid leukemia type M4. However, flow cytometry analysis revealed that CD7/CD56/CD33/CD34/HLA-DR/cCD3 were all positive and myeloperoxidase- (MPO-) specific staining, other T cells, NK cells, and myeloid markers were all negative. Clonal T-cell receptor (TCR)/TCR/TCR gene rearrangements and Epstein-Barr virus (EBV) were negative. The diagnosis of M/NKPAL was therefore confirmed. Unfortunately, this patient did not receive chemotherapy and later died of acute left heart failure and respiratory failure. SS complication with M/NKPAL is relatively rare. Combined with the relevant literatures, our study offers new insights into the clinical characteristics, pathological features, possible pathogenesis, and differential diagnosis of this rare disease.
我们报告1例干燥综合征(SS)合并髓系/自然杀伤(NK)细胞前体急性白血病(M/NKPAL)的病例。一名有2年SS病史的75岁女性接受常规治疗。外周血祖细胞增多,随后的骨髓细胞形态学检查显示存在M4型急性髓系白血病。然而,流式细胞术分析显示CD7/CD56/CD33/CD34/HLA-DR/cCD3均为阳性,而髓过氧化物酶(MPO)特异性染色、其他T细胞、NK细胞和髓系标志物均为阴性。克隆性T细胞受体(TCR)/TCR/TCR基因重排及EB病毒(EBV)均为阴性。因此确诊为M/NKPAL。不幸的是,该患者未接受化疗,后来死于急性左心衰竭和呼吸衰竭。SS合并M/NKPAL较为罕见。结合相关文献,我们的研究为这种罕见疾病的临床特征、病理特征、可能的发病机制及鉴别诊断提供了新的见解。