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Updated: Jan 25, 2026

Chromogenic In Situ Hybridization as a Tool for HPV-Related Head and Neck Cancer Diagnosis
Published on: June 14, 2019
Primary HPV cervical cancer screening in the United States: Are we ready?
Ritu Nayar1, Robert A Goulart2, Diane D Davey3
1Department of Pathology, Northwestern University Feinberg School of Medicine. Medical Director for Cytopathology, Northwestern Memorial Hospital, Chicago, Illinois.
Abstract:
In September 2017, the United States Preventive Services Task Force put forth updated draft guidelines for cervical cancer screening in the United States, which were then open to public comment. The recommendations allowed for every-3-year cervical cytology screening in women aged 21 to 65 years with an option for every-5-year high-risk human papillomavirus testing in women aged 30 to 65 years. There was no option for cotesting. Other recommendations were similar to those published by other professional organizations. The Cytopathology Education and Technology Consortium provided an official response during the open comment period, which is summarized here along with additional commentary by the authors.
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