BACKGROUNDRapid prescreening (RPS) is one of the quality assurance (QA) methods used in gynecologic cytology. The efficacy of RPS has been previously studied but mostly with respect to squamous lesions; in fact, there has been no study so far specifically looking at the sensitivity of RPS for detecting glandular cell abnormalities. METHODSA total of 80,565 Papanicolaou (Pap) smears underwent RPS during a 25-month period. A sample was designated as review for abnormality (R) if any abnormal cells (at the threshold of atypical squamous cells of undetermined significance/atypical glandular cells [AGC]) were thought to be present or was designated as negative (N) if none were detected. Each sample then underwent full screening (FS) and was designated as either R or N and also given a cytologic interpretation. RESULTSThe final cytologic interpretation was a glandular cell abnormality (AGC) in 107 samples (0.13%); 39 of these (36.4%) were flagged as R on RPS. Twenty-four patients (33.8%) out of 71 who had histologic follow-up were found to harbor a high-grade squamous intraepithelial lesion or carcinoma; 13 of those 24 Pap smears (54.2%) had been flagged as R on RPS. Notably, 11 AGC cases were picked up by RPS only and not by FS and represented false-negative cases; 2 of these showed endometrial adenocarcinoma on histologic follow-up. CONCLUSIONSPap smears with glandular cell abnormalities are often flagged as abnormal by RPS, and this results in a sensitivity of 36.4% (at the AGC threshold). Most importantly, some cases of AGC are detected on Pap smears by RPS only, and this demonstrates that RPS is a valuable QA method. Cancer (Cancer Cytopathol) 2015;123:739-744. (c) 2015 American Cancer Society. A significant fraction (36.4%) of atypical glandular cell lesions are identified by rapid prescreening; some of these (10.3%) are picked up by rapid prescreening only (and not by full screening). Rapid prescreening helps to reduce the false-negative rate of atypical glandular cells in gynecologic cytology.
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Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Medis Med Ctr, Iasi, RomaniaGrigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Gafitanu, D.
Scripcariu, Sadiye-Ioana
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Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, RomaniaGrigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Scripcariu, Sadiye-Ioana
Lazar, T.
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Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Medis Med Ctr, Iasi, RomaniaGrigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Lazar, T.
Teleman, S.
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Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Morpho Funct Sci 1, Iasi, RomaniaGrigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Teleman, S.
Grigore, Mihaela
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Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania
Grigore T Popa Univ Med & Pharm Iasi, Fac Med, Medis Med Ctr, Iasi, RomaniaGrigore T Popa Univ Med & Pharm Iasi, Fac Med, Dept Mother & Child Med, Iasi, Romania