1999
DOI: 10.1002/(sici)1097-0142(19991025)87:5<245::aid-cncr2>3.0.co;2-0
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Cytologic and cytochemical features of adenoma malignum of the uterine cervix

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Cited by 67 publications
(57 citation statements)
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References 17 publications
(10 reference statements)
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“…However, it will be difficult to differentiate lobular endocervical glandular hyperplasia from minimal deviation adenocarcinoma solely based on mucin colors since golden-yellow cytoplasmic mucin also has been suggested as representing the cytological features of minimal deviation adenocarcinoma. 57 We found intranuclear cytoplasmic inclusions in the lobular endocervical glandular hyperplasia cells in all four cases, but did not detect them in cancer cells. Since we have found no reports of these inclusions in other glandular lesions of the uterine cervix, this nuclear finding might be one of the cytological characteristics of lobular endocervical glandular hyperplasia.…”
Section: Endocervical Adenocarcinoma With Hyperplasiamentioning
confidence: 67%
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“…However, it will be difficult to differentiate lobular endocervical glandular hyperplasia from minimal deviation adenocarcinoma solely based on mucin colors since golden-yellow cytoplasmic mucin also has been suggested as representing the cytological features of minimal deviation adenocarcinoma. 57 We found intranuclear cytoplasmic inclusions in the lobular endocervical glandular hyperplasia cells in all four cases, but did not detect them in cancer cells. Since we have found no reports of these inclusions in other glandular lesions of the uterine cervix, this nuclear finding might be one of the cytological characteristics of lobular endocervical glandular hyperplasia.…”
Section: Endocervical Adenocarcinoma With Hyperplasiamentioning
confidence: 67%
“…Second, confusion on the diagnosis of benign hyperplastic lesions and minimal deviation adenocarcinoma might elicit an increased number of lobular endocervical glandular hyperplasia diagnoses. Since Ishii and co-workers 30,32,57 described the cytological and histological features of minimal deviation adenocarcinoma, we have actively interpreted golden-yellow mucin in Pap smears and gastric mucin in histological specimens (findings are now thought to be nonspecific for minimal deviation adenocarcinoma) as indicators of minimal deviation adenocarcinoma. Third, for the purpose of finding the early stage of minimal deviation adenocarcinoma, we tested a vaginal discharge screening test using enzyme-linked immunosorbent assay for HIK1083 in gynecology outpatients.…”
Section: Endocervical Adenocarcinoma With Hyperplasiamentioning
confidence: 99%
“…A cytological diagnosis was made according to the Bethesda system. Gastric‐type mucin in the cervical mucus was examined using a latex agglutination assay (HIK1083 kit)26 or by the detection of ‘yellow’ or ‘orange’ mucin in the cervical Pap smear 4. A clinical diagnosis and subsequent treatment were summarized as follows: the patient's condition was regarded as suspicious of MDA or adenocarcinoma (S/O MDA‐Ca) when pelvic MRI revealed a predominant solid component or invasive lesion and/or atypical glandular cells (AGC) in the Pap smear.…”
Section: Methodsmentioning
confidence: 99%
“…2,3 This antibody has since then been regarded as a promising diagnostic tool for MDAs. 4,5 However, its usefulness has been in dispute and Mikami et al 6,7 have demonstrated HIK1083 reactivity in pyloric gland metaplasia (PGM) of the cervix, which was described as lobular endocervical glandular hyperplasia (LEGH) by Nucci et al 8,9 These facts have provoked controversy concerning a possible link between LEGH/ PGM and MDA, and whether gastric phenotype is specific for these two conditions. In the current study, we have examined cervical adenocarcinomas including MDAs, adenocarcinoma in situ (AIS), and LEGH/PGM as well as a variety of benign glandular lesions to determine the incidence of gastric phenotypes and to shed light on the issue of histogenesis of MDA, employing antibodies to apomucins encoded by the MUC gene family, CD10 and chromogranin A (CGA), and HIK1083 and anti-p16 INK4 , the last for showing any relationship to high-risk HPV.…”
mentioning
confidence: 99%