2003
DOI: 10.1080/00313020307558
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Predictive value of diagnoses of endocervical glandular abnormalities in cervical smears

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Cited by 5 publications
(7 citation statements)
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“…There has Address correspondence and reprint requests to Rita Demopoulos, 24 Sycamore Road, Scarsdale, New York 10583. E-mail: rita.demopoulos@ med.nyu.edu (4)(5)(6)(7)(8)(9)(10). However, we found no studies in the literature that focused on the truly negative Pap smears in patients with invasive endocervical adenocarcinoma, which correlated the Pap smears with the pathology findings for a possible explanation.…”
mentioning
confidence: 74%
“…There has Address correspondence and reprint requests to Rita Demopoulos, 24 Sycamore Road, Scarsdale, New York 10583. E-mail: rita.demopoulos@ med.nyu.edu (4)(5)(6)(7)(8)(9)(10). However, we found no studies in the literature that focused on the truly negative Pap smears in patients with invasive endocervical adenocarcinoma, which correlated the Pap smears with the pathology findings for a possible explanation.…”
mentioning
confidence: 74%
“…20 Unfortunately, however, this new nomenclature has not solved the basic problem, how to improve the accuracy of cytologic diagnosis of cervical AC and its precursor lesions. 8,12,13,[18][19][20][21] With increasing evidence suggesting the etiolog- ic role of oncogenic human papillomaviruses (HPVs) in cervical AC, 8,22 the recent past has witnessed an influx of reports implicating the utility of HPV testing in the diagnosis of AIS, AC and their precursors. 23,24 This is exactly what happened few years earlier for SCC and its precursors, when Pap smear screening was recommended to be replaced or supplemented by HPV testing; that debate still continues.…”
Section: Editorialmentioning
confidence: 99%
“…8 However, the fact that AIS patients are older than women with squamous CIS 27 and that the reverse is true for AC and SCC 16 could imply that the progression of CGIN to AIS must be more slow than the progression of CIN lesions to CIS; in contrast, AIS should progress to invasive AC significantly more rapidly than does CIS into SCC, and that, indeed, seems to be the case. 31 This would leave ample time for detection of CGIN (but not necessarily AIS), 31 provided that the glandular precursor lesions can be accurately diagnosed 8,12,13,[17][18][19][20][21] and that screening coverage is adequate. [1][2][3][4] To answer the question in the title of this editorial, one can conclude that any measures increasing the coverage of screening and the accuracy of cytologic diagnosis of glandular precursor lesions (CGIN, AIS) would contribute toward reduction of the incidence of, morbidity from and mortality from invasive AC.…”
Section: Editorialmentioning
confidence: 99%
“…Therefore, policy formation about the appropriate investigation of women with these abnormalities must rely upon Australian publications. Recent Australian publications have been made by laboratories in Western Australia and New South Wales 8–12 …”
Section: Discussionmentioning
confidence: 99%
“…Segal et al 10 evaluated the positive predictive value of cytology reports issued between 1992 and 1998, with follow‐up histology usually within 6–24 months but ranging up to 9 years. Among nine cases in which the cytology was reported as definite AIS, seven (78%) were confirmed on histology as having high‐grade disease.…”
Section: Discussionmentioning
confidence: 99%