| Literature DB >> 34873649 |
Michiyasu Miki1, Yoshihiro Imaeda2, Hiroshi Takahashi3, Aya Iwata1, Tetsuya Tsukamoto2, Hiroyuki Nomura1, Kiriko Kotani1, Takeji Mitani1, Ryoko Ichikawa1, Takuma Fujii4.
Abstract
BACKGROUND: As the population ages in developed countries, the number of Pap smears for cervical cancer screening of older women is increasing. There is concern that cervical atrophy may cause misinterpretation of results for this segment of the population. The present study evaluated the accuracy of screening for high-grade intraepithelial lesions (HSILs) in women younger or older than 50 years, to determine whether aging affects cytological interpretation.Entities:
Keywords: Aging; Atrophy; Cervical cancer; Cytology; Screening
Mesh:
Year: 2021 PMID: 34873649 PMCID: PMC8816739 DOI: 10.1007/s10147-021-02065-w
Source DB: PubMed Journal: Int J Clin Oncol ISSN: 1341-9625 Impact factor: 3.402
Fig. 1Flow chart of eligible patients. Patients were enrolled from April 2009 to March 2016 in our institution. For the interpretation of HSILs, 647 patients with colposcopy-directed punch biopsies were enrolled in Group A. Of those, 286 patients underwent cone resection (Group B). Details are provided in the Materials and Methods. 1) Specimen provided on the first visit was used for the study if multiple specimens were collected in follow-up visits. Multiple specimens from the same patients were excluded
Association between age group and final histology results
| Histology | Young | Old | Total | |||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 20–29 | 30–39 | 40–49 | Subtotal | 50–59 | 60–69 | 70–79 | 80- | Subtotal | ||
Chronic cervicitis | 2 | 10 | 14 | 26 | 6 | 3 | 4 | 1 | 14 | 40 |
| CIN1 | 7 | 16 | 21 | 44 | 12 | 4 | 3 | 0 | 19 | 63 |
| CIN2 | 31 | 78 | 54 | 163 | 8 | 6 | 0 | 1 | 15 | 178 |
| CIN3 | 57 | 146 | 89 | 292 | 12 | 9 | 5 | 1 | 27 | 319 |
| Cancer | 3 | 8 | 16 | 27 | 9 | 7 | 4 | 0 | 20 | 47 |
| Total | 100 | 258 | 194 | 552 | 47 | 29 | 16 | 3 | 95 | 647 |
| PPV (CIN2 +) | 91% | 90% | 82% | 87.3% | 62% | 76% | 56% | 67% | 65.2% | |
The final histology obtained by biopsy or cone resection were determined by the high-grade result
Fig. 2Distribution of final histology results between younger (median 36 years of age) and older women (60 of age) in HSIL. A: women aged 20–49 classified into chronic cervicitis + CIN1 (black) and CIN2 + (dot), B: women aged ≥ 50 classified into chronic cervicitis + CIN1 (black) and CIN2 + (dot). There was a significant difference (p < 0.001) between A and B. C: women aged 20–49 classified into Cancer (black dot), chronic cervicitis (gray) and CIN1-3 (white), B: women aged ≥ 50 classified into Cancer (black dot), chronic cervicitis (gray) and CIN1-3 (white). There was a significant difference (p < 0.001) between C and D
Histology results by biopsy VS cone
| Histology | All ages | Colposcopy-directed biopsy | All ages | Cone | ||
|---|---|---|---|---|---|---|
| Young (median 36) | Old (median 60) | Young (median 36) | Old (median 60) | |||
| Chronic cervicitis | 13 | 10 | 3 | 4 | 2 | 2 |
| CIN1 | 11 | 5 | 6 | 6 | 3 | 3 |
| CIN2 | 50 | 44 | 6 | 25 | 21 | 4 |
| CIN3 | 195 | 179 | 16 | 219 | 202 | 17 |
| Cancer | 18 | 10 | 8 | 32 | 19 | 13 |
| Othera | 0 | 0 | 0 | 1 | 1 | 0 |
| Total | 287 | 248 | 39 | 287 | 248 | 39 |
alobular endocervical glandular hyperplasia
Up-grade※ results in cone resection from biopsy between younger and older women
| Young | Old | |
|---|---|---|
| (median 36) | (median 60) | |
| Rate of up-grade ( +) | 7/248 (2.8%) | 5/39 (12.8%)# |
※Up-grade defines from CC and CIN1 to CIN3 and worse in the identical patients. #Statistically significant (p = 0.0037)
Fig. 3Interpretation of HSIL in older patients. Cytology from a patient with final histology results diagnosed as cervical cancer, A: low (× 10) and B: high (× 20) magnification. Cytology from a patient with final histology results indicating chronic cervicitis, C: low (× 10) and D: high (× 20) magnification. Atypical squamous cells in a syncytial pattern with enlarged hyperchromatic nuclei on a background of watery or inflammatory change, illustrating the difficulty of discriminating cancer from inflammatory change in both cytology specimens.