Cokeromyces recurvatus : A rare fungus in the Pap test of an asymptomatic woman

2021 ◽  
Author(s):  
Neha Khaitan ◽  
Christine N. Booth ◽  
Raza S. Hoda
Keyword(s):  
Pap Test ◽  
2007 ◽  
Vol 2 (04) ◽  
Author(s):  
N Kyriakopoulos ◽  
C Gavala ◽  
I Georgantis ◽  
S Patiakas ◽  
E Tsoukis ◽  
...  
Keyword(s):  

2020 ◽  
Vol 9 (6) ◽  
pp. S54-S55
Author(s):  
Amy Spiczka ◽  
Amy Ardisana ◽  
Rosemarie Demyan ◽  
Elizabeth Waibel ◽  
Raven Garris ◽  
...  

2011 ◽  
Vol 2 (2) ◽  
pp. 232-237
Author(s):  
Tryfon Rotsos ◽  
Chrysanthos Symeonidis ◽  
Mrinal Rana ◽  
James S. Deane

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Charlotte A. Brown ◽  
Johnannes Bogers ◽  
Shaira Sahebali ◽  
Christophe E. Depuydt ◽  
Frans De Prins ◽  
...  

Since the Pap test was introduced in the 1940s, there has been an approximately 70% reduction in the incidence of squamous cell cervical cancers in many developed countries by the application of organized and opportunistic screening programs. The efficacy of the Pap test, however, is hampered by high interobserver variability and high false-negative and false-positive rates. The use of biomarkers has demonstrated the ability to overcome these issues, leading to improved positive predictive value of cervical screening results. In addition, the introduction of HPV primary screening programs will necessitate the use of a follow-up test with high specificity to triage the high number of HPV-positive tests. This paper will focus on protein biomarkers currently available for use in cervical cancer screening, which appear to improve the detection of women at greatest risk for developing cervical cancer, including Ki-67,p16INK4a, BD ProEx C, and Cytoactiv HPV L1.


2021 ◽  
Vol 162 ◽  
pp. S153-S154
Author(s):  
Talayeh Ghezelayagh ◽  
Jeanne Fredrickson ◽  
Jeffrey Krimmel-Morrison ◽  
Brendan Kohrn ◽  
Marc Radke ◽  
...  

2014 ◽  
Vol 10 (1) ◽  
pp. 210
Author(s):  
Amitabh Jena ◽  
Rashmi Patnayak ◽  
SivaKumar Reddy
Keyword(s):  
Pap Test ◽  

2016 ◽  
Vol 60 (5) ◽  
pp. 445-450 ◽  
Author(s):  
Yiang Hui ◽  
Katrine Hansen ◽  
Jayasimha Murthy ◽  
Danielle Chau ◽  
C. James Sung ◽  
...  

Objective: A vast majority of cervicovaginal intraepithelial lesions are caused by high-risk human papillomaviruses (HPVs). The Pap test has been the sole method used for the screening of cervicovaginal squamous intraepithelial lesions (SIL). Recently, the FDA approved an HPV-DNA assay as a method of primary screening. We report on a series of FDA-approved HPV-DNA test-negative SIL with HPV genotyping, using an alternative method on the corresponding surgical biopsy specimens. Study Design: A retrospective review identified cytology-positive HPV-negative cases over a 15-month period at a tertiary care gynecologic oncology institution. Corresponding biopsies were reviewed and genotyped for high-risk HPVs. Results: Of the 18,200 total cases, 17 patients meeting the study criteria were selected with 27 surgical specimens corresponding to their cytologic diagnoses. Four patients with high-grade lesions were identified, 3 of whom (75%) were positive for HPV. One of these 4 patients (25%) showed high-grade SIL on biopsies from 4 separate sites in the cervix and vagina. Multiviral HPV infections were frequent. Conclusions: We discuss the relevance of cotesting for screening cervical SILs and emphasize that false-negative results are possible with the FDA-approved HPV screening assay, also in patients with high-grade SIL. These cases may be detectable by cytologic examination and this suggests that the Pap test remains an important diagnostic tool.


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