王梦园, 马莉, 管俊. 经多色流式细胞术确诊多发性骨髓瘤并发恶性胸腔积液6例临床特征分析[J]. 中国肿瘤临床, 2020, 47(17): 876-880. DOI: 10.3969/j.issn.1000-8179.2020.17.898
引用本文: 王梦园, 马莉, 管俊. 经多色流式细胞术确诊多发性骨髓瘤并发恶性胸腔积液6例临床特征分析[J]. 中国肿瘤临床, 2020, 47(17): 876-880. DOI: 10.3969/j.issn.1000-8179.2020.17.898
Mengyuan Wang, Li Ma, Jun Guan. Clinical features of multiple myeloma with malignant pleural effusion diagnosed using multicolor flow cytometry: a report of six cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(17): 876-880. DOI: 10.3969/j.issn.1000-8179.2020.17.898
Citation: Mengyuan Wang, Li Ma, Jun Guan. Clinical features of multiple myeloma with malignant pleural effusion diagnosed using multicolor flow cytometry: a report of six cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(17): 876-880. DOI: 10.3969/j.issn.1000-8179.2020.17.898

经多色流式细胞术确诊多发性骨髓瘤并发恶性胸腔积液6例临床特征分析

Clinical features of multiple myeloma with malignant pleural effusion diagnosed using multicolor flow cytometry: a report of six cases

  • 摘要:
      目的:  分析由多色流式细胞术(flow cytometry,FCM)诊断的多发性骨髓瘤(multiple myeloma,MM)并发恶性胸腔积液(my-eloma pleural effusion,MPE)患者的临床特点。
      方法:  回顾性分析江苏省苏北人民医院2016年7月至2020年5月经FCM确诊的6例MM并发MPE患者的临床特征、实验室指标和转归情况。
      结果:  6例患者中位发病年龄为62(49~72)岁,男女比为2:1。其中,IgA型3例,IgG型2例,轻链型1例,所有患者常规脱落细胞学检查均为阴性,但FCM均能找到浆细胞。随访截至2020年5月1日,4例患者死亡,2例患者存活。FCM检测胸水浆细胞比例与胸水总蛋白、白蛋白、球蛋白、乳酸脱氢酶(lactate dehydrogenase,LDH)水平、腺苷脱氨酶(adenosine deaminase,ADA)及初诊时骨髓浆细胞比例成正相关(P < 0.05),与胸水常规红细胞数、单个核细胞数、白细胞数以及血清血红蛋白、血小板、总蛋白、白蛋白、LDH水平、ADA、β2-微球蛋白均无明显相关性(P>0.05)。
      结论:  MM并发MPE的患者较少见,FCM诊断的阳性率明显高于常规脱落细胞学检查,可将其作为常规胸水检查的必要联合检查项目,此类患者生存期短,预后较差。

     

    Abstract:
      Objective:  To analyze the clinical characteristics of multiple myeloma (MM) with malignant pleural effusion (MPE) diagnosed using multicolor flow cytometry (FCM).
      Methods:  A total of six patients confirmed with MM with MPE diagnosed using FCM in the period from July 2016 to May 2020 at the Northern Jiangsu People's Hospital were enrolled in this retrospective study. The clinical characteristics, laboratory indicators, and treatment outcomes of the patients were analyzed.
      Results:  The median age at the time of diagnosis of the six patients with MM was 62 years (range:49-72 years), while the male-to-female ratio was 2:1. The MM isotype was IgA in three patients, IgG in two patients, and light chain myeloma in one patient. Malignant cells were not detected with conventional cytology in the pleural effusion of any patient confirmed with MM, but plasma cells were detected with FCM. By the final follow-up, four patients had died, whereas two had survived. The ratio of plasma cells diagnosed using multicolor FCM positively correlated with the pleural effusion protein, albumin, globulin, lactate dehydrogenase (LDH), and adenosine deaminase (ADA) as well as the ratio of abnormal plasma cells in the bone marrow (P>0.05). There were no correlations among the pleural effusion red blood cell count, mononuclear cell count, white blood cell count, hemoglobin, platelets, serum total protein, serum albumin, serum LDH, serum ADA, and blood β2-macroglobulin (P>0.05).
      Conclusions:  Malignant pleural effusion in MM patients is rare, and routine pleural effusion pathological examinations have a low sensitivity. The positive rate in MM with MPE is significantly higher in the multicolor FCM assay than in conventional cytology. Multicolor FCM may be useful for improving the detection rate of MPE. Therefore, multicolor FCM can be used in routine pleural effusion examinations. MM patients with MPE have a shorter survival time and poor prognosis.

     

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