Perspectives from Hysterectomy Specimens on the Hidden Malignancy Risk in HSIL Patients with Surgical Margin Continuity
Abstract
1. Introduction
2. Materials and Methods
Statistical Analysis
3. Results
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Ostör, A.G. Natural history of cervical intraepithelial neoplasia: A critical review. Int. J. Gynecol. Pathol. 1993, 12, 186–192. [Google Scholar] [CrossRef]
- Farzaneh, F.; Faghih, N.; Hosseini, M.S.; Arab, M.; Ashrafganjoei, T.; Bahman, A. Evaluation of neutrophil-lymphocyte ratio as a prognostic factor in cervical intraepithelial neoplasia recurrence. Asian Pac. J. Cancer Prev. 2019, 20, 2365–2372. [Google Scholar] [CrossRef]
- Oncins Torres, R.; Aragón Sanz, M.Á.; Clemente Roldán, E.; Comes García, M.D.; Muñiz Unamunzaga, G.; Guardia Dodorico, L.; Vallés Gallego, V. Estudio de piezas de conización tras cinco años de cribado de cáncer de cérvix con co-test [Study of conizations of the cervix after five years of cervical cancer screening with co-testing]. Rev. Esp. Salud Publica 2018, 92, e201810045. (In Spanish) [Google Scholar]
- Arbyn, M.; Redman, C.W.E.; Verdoodt, F.; Kyrgiou, M.; Tzafetas, M.; Ghaem-Maghami, S.; Petry, K.U.; Leeson, S.; Bergeron, C.; Nieminen, P.; et al. Incomplete excision of cervical precancer as a predictor of treatment failure: A systematic review and meta-analysis. Lancet Oncol. 2017, 18, 1665–1679. [Google Scholar] [CrossRef] [PubMed]
- Alder, S.; Megyessi, D.; Sundström, K.; Östensson, E.; Mints, M.; Belkić, K.; Arbyn, M.; Andersson, S. Incomplete excision of cervical intraepithelial neoplasia as a predictor of the risk of recurrent disease-a 16-year follow-up study. Am. J. Obstet. Gynecol. 2020, 222, 172.e1–172.e12. [Google Scholar] [CrossRef]
- Wu, Q.; Jiang, Y.; Ding, J.; Xia, L.; Xu, H. Clinical predictors of residual disease in hysterectomy following a loop electrosurgical excision procedure for cervical intraepithelial neoplasia grade 3. BMC Pregnancy Childbirth 2022, 22, 971. [Google Scholar] [CrossRef] [PubMed]
- American College of Obstetricians and Gynecologists. ACOG Practice Bulletin number 66, September 2005. Management of abnormal cervical cytology and histology. Obs. Gynecol. 2005, 106, 645–664. [Google Scholar] [CrossRef]
- Committee on Gynecologic Practice. Committee Opinion No 701: Choosing the route of hysterectomy for benign disease. Obstet. Gynecol. 2017, 129, e155–e159. [Google Scholar] [CrossRef]
- Wright, T.C., Jr.; Cox, J.T.; Massad, L.S.; Carlson, J.; Twiggs, L.B.; Wilkinson, E.J. 2001 ASCCP-sponsored Consensus Workshop. 2001 Consensus guidelines for the management of women with cervical intraepithelial neoplasia. J. Low. Genit. Tract Dis. 2003, 7, 154–167. [Google Scholar] [CrossRef]
- Peng, H.; Liu, W.; Jiang, J.; Du, H. Extensive lesions and a positive cone margin are strong predictors of residual disease in subsequent hysterectomy following conization for squamous intraepithelial lesion grade 2 or 3 study design. BMC Women’s Health 2023, 23, 454. [Google Scholar] [CrossRef]
- Perkins, R.B.; Guido, R.S.; Castle, P.E.; Chelmow, D.; Einstein, M.H.; Garcia, F.; Huh, W.K.; Kim, J.J.; Moscicki, A.B.; Nayar, R.; et al. 2019 ASCCP Risk-Based management consensus guidelines for abnormal cervical cancer screening tests and cancer precursors. J. Low. Genit. Tract Dis. 2020, 24, 102–131, Erratum in J. Low. Genit. Tract Dis. 2020, 24, 427. [Google Scholar] [CrossRef]
- Martin-Hirsch, P.P.; Paraskevaidis, E.; Bryant, A.; Dickinson, H.O. Surgery for cervical intraepithelial neoplasia. Cochrane Database Syst. Rev. 2013, 2013, CD001318. [Google Scholar] [CrossRef] [PubMed]
- Zhao, C.; Bi, H.; Zhao, Y. Chinese expert consensus on management of high-grade intraepithelial lesions of cervix. Chin. J. Obstet. Gynecol. 2022, 2, 220–224. [Google Scholar]
- Chinese Society of Gynecological Oncology. Clinical Practice Guidelines for Gynecological Malignancies in China, 6th ed.; Xie, X., Ma, D., Kong, B., Eds.; The People’s Health Press Co., Ltd.: Beijing, China, 2020. [Google Scholar]
- Lei, L.; Zhang, L.; Zheng, Y.; Ma, W.; Liu, F.; Li, D.; Chen, K.; Zeng, Y. Clinical analysis of 314 patients with high-grade squamous intraepithelial lesion who underwent total hysterectomy directly: A multi-center, retrospective cohort study. BMC Cancer 2024, 24, 575. [Google Scholar] [CrossRef]
- Ciavattini, A.; Di Giuseppe, J.; Marconi, C.; Giannella, L.; Delli Carpini, G.; Paolucci, M.; Fichera, M.; De Vincenzo, R.P.; Scambia, G.; Evangelista, M.T.; et al. Hysterectomy for cervical intraepithelial neoplasia: A retrospective observational multi-institutional study. Int. J. Gynaecol. Obstet. 2022, 159, 679–688. [Google Scholar] [CrossRef]
- Wang, J.; Wang, C.; Su, T. Risk factors for residual lesions after total hysterectomy in patients with high-grade cervical intraepithelial neoplasia. BMC Women’s Health 2024, 24, 369. [Google Scholar] [CrossRef]
- Zeng, Y.; Jiang, T.; Zheng, Y.; Yang, J.; Wei, H.; Yi, C.; Liu, Y.; Chen, K. Risk factors predicting residual lesion in subsequent hysterectomy following cold knife conization (CKC) for high-grade squamous intraepithelial lesion (HSIL). BMC Women’s Health 2022, 22, 358. [Google Scholar] [CrossRef] [PubMed]
- Sun, X.; Lei, H.; Xie, X.; Ruan, G.; An, J.; Sun, P. Risk factors for residual disease in hysterectomy specimens after conization in post-menopausal patients with cervical intraepithelial neoplasia grade 3. Int. J. Gen. Med. 2020, 13, 1067–1074. [Google Scholar] [CrossRef]
- Chan, C.K.; Aimagambetova, G.; Ukybassova, T.; Kongrtay, K.; Azizan, A. Human Papillomavirus infection and cervical cancer: Epidemiology, screening, and vaccination-review of current perspectives. J. Oncol. 2019, 2019, 3257939. [Google Scholar] [CrossRef]
- Wentzensen, N.; Clarke, M.A. Cervical cancer screening-past, present, and future. Cancer Epidemiol. Biomark. Prev. 2021, 30, 432–434. [Google Scholar] [CrossRef]
- Okazaki, C.; Focchi, G.R.; Taha, N.S.; Almeida, P.Q.; Schimidt, M.A.; Speck, N.M.; Ribalta, J.C. Depth of glandular crypts and its involvement in squamous intraepithelial cervical neoplasia submitted to large loop excision of transformation zone (LLETZ). Eur. J. Gynaecol. Oncol. 2013, 34, 48–50. [Google Scholar]
- Kır, G.; Karabulut, M.H.; Topal, C.S.; Yılmaz, M.S. Endocervical glandular involvement, positive endocervical surgical margin and multicentricity are more often associated with high-grade than low-grade squamous intraepithelial lesion. J. Obstet. Gynaecol. Res. 2012, 38, 1206–1210. [Google Scholar] [CrossRef]
- Kim, N.R.; Baek, Z.H.; Lee, A.J.; Yang, E.J.; Ouh, Y.T.; Kim, M.K.; Shim, S.H.; Lee, S.J.; Kim, T.J.; So, K.A. Clinical Outcomes Associated with Endocervical Glandular Involvement in Patients with Cervical Intraepithelial Neoplasia III. J. Clin. Med. 2022, 11, 2996. [Google Scholar] [CrossRef]
- Brown, L.D.; Cai, T.T.; DasGupta, A. Interval estimation for a binomial proportion. Stat. Sci. 2001, 16, 101–133. [Google Scholar] [CrossRef]
- Newcombe, R.G. Two-sided confidence intervals for the single proportion: Comparison of seven methods. Stat. Med. 1998, 17, 857–872. [Google Scholar] [CrossRef]
- Altman, D.G.; Deeks, J.J.; Sackett, D.L. Odds ratios should be avoided when events are common. BMJ 1998, 317, 1318, Erratum in BMJ 1998, 317, 1505. [Google Scholar] [CrossRef] [PubMed]

| Parameter | N (%) or Mean ± SD | 95% CI |
|---|---|---|
| Age | 46.7 ± 8.3 | - |
| BMI (kg/m2) | 27.4 ± 2.3 | - |
| Parity | 2.5 ± 0.7 | - |
| Menopausal Status | ||
| Premenopausal | 17 (50) | 34.1–65.9 |
| Postmenopausal | 17 (50) | 34.1–65.9 |
| Smoking History | ||
| Yes | 21 (61.8) | 45.0–76.1 |
| No | 13 (38.2) | 23.9–55.0 |
| Transformation Zone Type | ||
| Type 1 | 13 (38.2) | 23.9–55.0 |
| Type 2 | 17 (50) | 34.1–65.9 |
| Type 3 | 4 (11.8) | 4.7–26.6 |
| Cytology (Pap Smear) Findings | ||
| Normal | 21 (61.8) | 45.0–76.1 |
| ASC-US | 8 (23.5) | 12.4–40.0 |
| ASC-H | 5 (14.7) | 6.4–30.1 |
| AGUS | 0 (0) | - |
| LSIL | 0 (0) | - |
| HSIL | 0 (0) | - |
| SCC | 0 (0) | - |
| HPV Genotype | ||
| Type 16 | 24 (70.6) | 53.8–83.2 |
| Type 18 | 4 (11.8) | 4.7–26.6 |
| Type 33 | 2 (5.9) | 1.6–19.1 |
| Type 45 | 2 (5.9) | 1.6–19.1 |
| Type 56 | 1 (2.9) | 0.5–14.9 |
| Types 16 and 45 | 1 (2.9) | 0.5–14.9 |
| Parameter | N (%) | 95% CI |
|---|---|---|
| Colposcopic Biopsy Result | ||
| CIN2 | 7 (20.6) | 10.4–36.2 |
| CIN3 | 27 (79.4) | 63.8–89.6 |
| LEEP + ECC Histopathology Result (All CIN3) | ||
| Ectocervical Margin Positive | 23 (67.6) | 50.8–80.9 |
| Endocervical Margin Positive | 0 (0) | - |
| Combine Margin Positive | 11 (32.4) | 19.1–49.2 |
| Negative | 0 (0) | - |
| Post-LEEP CKC + ECC Histopathology Result (All CIN3) | ||
| Ectocervical Margin Positive | 21 (61.8) | 45.0–76.1 |
| Endocervical Margin Positive | 0 (0) | - |
| Combine Margin Positive | 13 (38.2) | 23.9–55.0 |
| Negative | 0 (0) | - |
| Hysterectomy Histopathology | ||
| CIN2 | 8 (23.5) | 12.4–40.0 |
| CIN3 | 19 (55.9) | 39.5–71.1 |
| Adenocarcinoma In Situ | 3 (8.8) | 3.0–23.0 |
| Squamous Cell Carcinoma | 4 (11.8) | 4.7–26.6 |
| Glandular Involvement in Hysterectomy Specimens | ||
| Present | 13 (38.2) | 23.9–55.0 |
| Absent | 21 (61.8) | 45.0–76.1 |
| Surgical Margin Status in Hysterectomy Specimens | ||
| Negative | 34 (100) | - |
| Positive | 0 (0) |
| Patient No. | Age | Smoking Status | HPV Type | Smear | Colposcopic Biopsy Histopathology | Hysterectomy Histopathology | Glandular Involvement |
|---|---|---|---|---|---|---|---|
| 1 | 41 | Positive | 16 | HSIL | CIN3 | SCC | Positive |
| 2 | 36 | Positive | 16, 45 | Normal | CIN3 | SCC | Positive |
| 3 | 46 | Positive | 16 | HSIL | CIN3 | SCC | Positive |
| 4 | 39 | Positive | 16 | HSIL | CIN3 | SCC | Negative |
| 5 | 47 | Negative | 18 | Normal | CIN3 | AIS | Positive |
| 6 | 49 | Positive | 18 | Normal | CIN3 | AIS | Positive |
| 7 | 46 | Positive | 16 | ASC-US | CIN3 | AIS | Negative |
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Görgülü, G.; Sanci, M. Perspectives from Hysterectomy Specimens on the Hidden Malignancy Risk in HSIL Patients with Surgical Margin Continuity. Medicina 2026, 62, 77. https://doi.org/10.3390/medicina62010077
Görgülü G, Sanci M. Perspectives from Hysterectomy Specimens on the Hidden Malignancy Risk in HSIL Patients with Surgical Margin Continuity. Medicina. 2026; 62(1):77. https://doi.org/10.3390/medicina62010077
Chicago/Turabian StyleGörgülü, Gökşen, and Muzaffer Sanci. 2026. "Perspectives from Hysterectomy Specimens on the Hidden Malignancy Risk in HSIL Patients with Surgical Margin Continuity" Medicina 62, no. 1: 77. https://doi.org/10.3390/medicina62010077
APA StyleGörgülü, G., & Sanci, M. (2026). Perspectives from Hysterectomy Specimens on the Hidden Malignancy Risk in HSIL Patients with Surgical Margin Continuity. Medicina, 62(1), 77. https://doi.org/10.3390/medicina62010077

