Diagnostic benefits of the combined use of liquid-based cytology, cell block, and carcinoembryonic antigen immunocytochemistry in malignant pleural effusion

被引:22
作者
Woo, Chang Gok [1 ]
Son, Seung-Myoung [1 ]
Han, Hye-Suk [2 ,3 ]
Lee, Ki Hyeong [2 ,3 ]
Choe, Kang-Hyeon [2 ,3 ]
An, Jin Young [2 ,3 ]
Lee, Ki Man [2 ,3 ]
Lim, Young Hyun [3 ]
Lee, Ho-Chang [1 ,3 ]
Lee, Ok-Jun [1 ,3 ]
机构
[1] Chungbuk Natl Univ Hosp, Dept Pathol, Cheongju, South Korea
[2] Chungbuk Natl Univ Hosp, Dept Internal Med, Cheongju, South Korea
[3] Chungbuk Natl Univ, Coll Med, Cheongju, South Korea
基金
新加坡国家研究基金会;
关键词
Cytology; cell block (CB); immunotrochemistry; carcinoembryonic antigen (CEA); Malignant pleural effusion (MPE); SEROUS EFFUSIONS; FLUID CYTOLOGY; CONVENTIONAL SMEAR; MESOTHELIAL CELLS; LUNG-CANCER; IMMUNOHISTOCHEMISTRY; CELLPREPPLUS(R); CYFRA-21-1; COLLEGE; UTILITY;
D O I
10.21037/jtd.2018.07.139
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Malignant pleural effusion (MPE) is a common complication of cancer cell metastasis to the pleura. Discrimination between MPE and benign pleural effusion is necessary to design treatment strategies. Cytology is important for the diagnosis of MPE. Carcinoembryonic antigen (CEA) is an epithelial biomarker with a strong staining pattern in adenocarcinomas. Here, the diagnostic performances of liquid-based cytology (LBC), cell block (CB) preparation, and CEA immunostaining for the detection of malignancy in effusion cytology were compared in a large case series. Methods: In a single institution, 1,014 cytology samples from 862 patients were retrospectively collected and reviewed between January 2013 and November 2015. Ethanol-fixed, paraffin embedded CB of pleural effusions was analyzed by CEA immunostaining. Diagnostic values were compared among LBC, CB, CEA immunostaining, and the combination of two methods. Results: The sensitivity and specificity of the CB preparation were 94.3% and 98.7%, respectively, compared with 81.3% and 99.4% for LBC preparations, respectively. Combination of LBC and CB increased sensitivity by 98.3%. Although the accuracy of CEA staining itself was moderate (sensitivity, 89.8%), the combined use of CB and CEA tumor marker increased the detection rate of malignancy (sensitivity, 100%; specificity, 100%), compared with that of cytology (LBC or CB) alone. Conclusions: The sensitivity and specificity for the diagnosis of MPE could be improved by integrating the CB and CEA staining into LBC in routine clinical practice to improve diagnostic accuracy.
引用
收藏
页码:4931 / 4939
页数:12
相关论文
共 28 条
  • [1] Diagnostic value of CEA, CA 15-3, CA 19-9, CYFRA 21-1, NSE and TSA assay in pleural effusions
    Alatas, F
    Alatas, Ö
    Metintas, M
    Çolak, Ö
    Harmanci, E
    Demir, S
    [J]. LUNG CANCER, 2001, 31 (01) : 9 - 16
  • [2] A comparative study of conventional cytology and cell block method in the diagnosis of pleural effusion
    Assawasaksakul, Theerada
    Boonsarngsuk, Viboon
    Incharoen, Pimpin
    [J]. JOURNAL OF THORACIC DISEASE, 2017, 9 (09) : 3161 - 3167
  • [3] Bedrossian CWM, 1998, DIAGN CYTOPATHOL, V19, P131, DOI 10.1002/(SICI)1097-0339(199808)19:2<131::AID-DC14>3.0.CO
  • [4] 2-G
  • [5] DEKKER A, 1978, AM J CLIN PATHOL, V70, P855
  • [6] Utility of cell block to detect malignancy in fluid cytology: Adjunct or necessity?
    Dey, Sumedha
    Nag, Dipanwita
    Nandi, Ayandip
    Bandyopadhyay, Ranjana
    [J]. JOURNAL OF CANCER RESEARCH AND THERAPEUTICS, 2017, 13 (03) : 425 - 429
  • [7] Elsamany Shereef Ahmed, 2015, Asian Pac J Cancer Prev, V16, P2987
  • [8] Immunohistochemistry Practices of Cytopathology Laboratories A Survey of Participants in the College of American Pathologists Nongynecologic Cytopathology Education Program
    Fischer, Andrew H.
    Schwartz, Mary R.
    Moriarty, Ann T.
    Wilbur, David C.
    Souers, Rhona
    Fatheree, Lisa
    Booth, Christine N.
    Clayton, Amy C.
    Kurtyz, Daniel F. I.
    Padmanabhan, Vijayalakshmi
    Crothers, Barbara A.
    [J]. ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2014, 138 (09) : 1167 - 1172
  • [9] Fowler LJ, 2008, ARCH PATHOL LAB MED, V132, P373, DOI 10.1043/1543-2165(2008)132[373:AOITC]2.0.CO
  • [10] 2