Assessing for Primary Oropharyngeal or Nasopharyngeal Squamous Cell Carcinoma From Fine Needle Aspiration of Cervical Lymph Node Metastases

被引:43
作者
Jannapureddy, Suneal [1 ]
Cohen, Cynthia [1 ]
Lau, Stephen [2 ]
Beitler, Jonathan J. [3 ]
Siddiqui, Momin T. [1 ]
机构
[1] Emory Univ Hosp, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[2] Vet Affairs Med Ctr, Dept Pathol & Lab Med, Atlanta, GA 30033 USA
[3] Emory Univ Hosp, Dept Radiat Oncol, Atlanta, GA 30322 USA
关键词
metastatic neck squamous cell carcinoma; HPV16/18; oropharyngeal squamous cell carcinoma; tonsillar squamous cell carcinoma; IN-SITU HYBRIDIZATION; HUMAN-PAPILLOMAVIRUS; NECK; HEAD; P16(INK4A);
D O I
10.1002/dc.21293
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
In fine needle aspirates of cervical lymph nodes with metastatic squamous cell carcinoma (SCC), the site of origin may not be clinically evident. The distinction between oropharyngeal and nasopharyngeal primary SCC has important management consequences. In the current study, we evaluated metastatic SCC for HPV types 16, 18, 31, 33, 51 (by in situ hybridization[ISH]), p16 and ProExC (surrogate HPV markers), and Epstein Barr Virus reported in nasopharyngeal SCC. Forty patients diagnosed between 2004 and 2008, with adequate cell block material were identified. ISH for high risk HPV and EBV (EBER), and immunohistochemistry for p16 and ProExC were performed. Primary site was designated in 31 cases with 26 head and Fleck including 11 oropharyngeal and 2 nasopharyngeal, and 5 other sites. High risk HPV was detected in 9 cases (22.5%), p16 in 16 (40%), ProExC in 35 (87.5%), and EBER in 2 (5%). All cases with high risk HPV ISH also showed overexpression of p16. The sensitivity for HPV infection by both surrogate markers was 100%: specificity for p16 and ProExC was 78.7 and 16.1%, respectively. Seven (63.6%) oropharyngeal SCC were positive for HPV ISH and negative for EBV; one nasopharyngeal SCC (50%) was EBER positive and HPV negative. HPV and EBER detection can serve as indicators for oropharyngeal and nasopharyngeal primary SCC, respectively, however our data show that only a subset (63.6%) of oropharyngeal SCC are high risk HPV-related. Additionally, despite their high sensitivity for HPV infection, surrogate markers, especially ProExC, lack specificity. Diagn. Cytopathol. 2010;38:795-800. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:795 / 800
页数:6
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