Contralateral ovarian endometrioma recurrence after unilateral salpingo-oophorectomy

Tokie Hidari, Tetsuya Hirata, Tomoko Arakawa, Kaori Koga, Kazuaki Neriishi, Shinya Fukuda, Akari Nakazawa, Natsuki Nagashima, Suke Ma, Hui Sun, Masashi Takamura, Miyuki Harada, Yasushi Hirota, Osamu Wada-Hiraike, Tomoyuki Fujii, Yutaka Osuga, Tokie Hidari, Tetsuya Hirata, Tomoko Arakawa, Kaori Koga, Kazuaki Neriishi, Shinya Fukuda, Akari Nakazawa, Natsuki Nagashima, Suke Ma, Hui Sun, Masashi Takamura, Miyuki Harada, Yasushi Hirota, Osamu Wada-Hiraike, Tomoyuki Fujii, Yutaka Osuga

Abstract

Background: The recurrence rate after unilateral salpingo-oophorectomy (USO) for unilateral endometrioma has not been reported. We evaluated the rate of and risk factors for endometrioma recurrence after USO.

Methods: In this retrospective observational study, we enrolled 110 women (age, 35-45 years) who underwent laparoscopic USO (n = 50) or cystectomy (n = 60) for unilateral ovarian endometrioma from January 2010 through December 2012. We compared patients' characteristics between patients who underwent USO and those who underwent cystectomy. We also compared patients with and without an endometrioma recurrence after USO using univariate and multivariate stepwise logistic regression models to identify recurrence risk factors. Endometrioma recurrence was defined as an ovarian cyst (> 2 cm) with features typical of an endometrioma identified by postoperative transvaginal sonography.

Results: Endometrioma recurred in 8 (16%) patients after USO (mean follow-up, 46.0 ± 12.9 months [range, 15-73]). The post-USO cumulative recurrence rates at 12, 24, 36, and 60 months were 8.0, 10.2, 12.7, and 24.7%, respectively (Kaplan-Meier analysis). In logistic regression analysis, a contralateral side adhesion score ≥ 4 was an independent risk factor for endometrioma recurrence after USO (odds ratio, 19.48, 95% confidence interval, 1.59-237.72). The post-USO cumulative recurrence rates at 12, 24, 36, and 57 months were 19.5, 24.1, 31.0, and 54.0%, respectively, in cases with contralateral side adhesion scores ≥4, and 0.0, 0.0, 0.0, and 5.9%, respectively, in cases with scores < 4 (log-rank test, P = 0.0023).

Conclusions: To our knowledge, this is the first report on the recurrence rate and risk factors associated with recurrence after USO. Endometrioma recurrence rates were 24.7% during the first 5 years after USO. The post-USO recurrence rate increased significantly in cases with contralateral side adhesions. Our findings could improve the planning of USO and patient selection for postoperative hormonal therapy.

Keywords: Endometriosis; Recurrence; Unilateral endometrioma; Unilateral salpingo-oophorectomy.

Conflict of interest statement

Ethics approval and consent to participate

This study was approved by the Institutional Review Board of Tokyo University Hospital. We obtained written informed consent from all participants before surgery.

Consent for publication

All participants provided written informed consent to publish the information.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Kaplan-Meier analysis of endometrioma recurrence after unilateral salpingo-oophorectomy. There was a significant difference in recurrence in patients with a contralateral adhesion score ≥ 4 and those with contralateral adhesion score P = 0.0023, log-rank test)

References

    1. Zondervan KT, Becker CM, Koga K, Missmer SA, Taylor RN, Vigano P. Endometriosis. Nat Rev Dis Primers. 2018;4(1):9. doi: 10.1038/s41572-018-0008-5.
    1. Giudice LC, Kao LC. Endometriosis. Lancet. 2004;364(9447):1789–1799. doi: 10.1016/S0140-6736(04)17403-5.
    1. Vercellini P, Vigano P, Somigliana E, Fedele L. Endometriosis: pathogenesis and treatment. Nat Rev Endocrinol. 2014;10(5):261–275. doi: 10.1038/nrendo.2013.255.
    1. Chapron C, Vercellini P, Barakat H, Vieira M, Dubuisson JB. Management of ovarian endometriomas. Hum Reprod Update. 2002;8(6):591–597. doi: 10.1093/humupd/8.6.591.
    1. Koga K, Takamura M, Fujii T, Osuga Y. Prevention of the recurrence of symptom and lesions after conservative surgery for endometriosis. Fertil Steril. 2015;104(4):793–801. doi: 10.1016/j.fertnstert.2015.08.026.
    1. Guo SW. Recurrence of endometriosis and its control. Hum Reprod Update. 2009;15(4):441–461. doi: 10.1093/humupd/dmp007.
    1. Kim ML, Kim JM, Seong SJ, Lee SY, Han M, Cho YJ. Recurrence of ovarian endometrioma after second-line, conservative, laparoscopic cyst enucleation. Am J Obstet Gynecol. 2014;210(3):216 e211–216 e216. doi: 10.1016/j.ajog.2013.11.007.
    1. Laughlin-Tommaso SK, Stewart EA, Grossardt BR, Rocca LG, Rocca WA. Incidence, time trends, laterality, indications, and pathological findings of unilateral oophorectomy before menopause. Menopause. 2014;21(5):442–449. doi: 10.1097/GME.0b013e3182a3ff45.
    1. Revised American Society for Reproductive Medicine classification of endometriosis: 1996. Fertil Steril. 1997;67(5):817–821.
    1. Koga K, Takemura Y, Osuga Y, Yoshino O, Hirota Y, Hirata T, Morimoto C, Harada M, Yano T, Taketani Y. Recurrence of ovarian endometrioma after laparoscopic excision. Hum Reprod. 2006;21(8):2171–2174. doi: 10.1093/humrep/del125.
    1. Takamura M, Koga K, Osuga Y, Takemura Y, Hamasaki K, Hirota Y, Yoshino O, Taketani Y. Post-operative oral contraceptive use reduces the risk of ovarian endometrioma recurrence after laparoscopic excision. Hum Reprod. 2009;24(12):3042–3048. doi: 10.1093/humrep/dep297.
    1. Haraguchi H, Koga K, Takamura M, Makabe T, Sue F, Miyashita M, Urata Y, Izumi G, Harada M, Hirata T, et al. Development of ovarian cancer after excision of endometrioma. Fertil Steril. 2016;106(6):1432–7 e1432. doi: 10.1016/j.fertnstert.2016.07.1077.
    1. Van Holsbeke C, Van Calster B, Guerriero S, Savelli L, Paladini D, Lissoni AA, Czekierdowski A, Fischerova D, Zhang J, Mestdagh G, et al. Endometriomas: their ultrasound characteristics. Ultrasound Obstet Gynecol. 2010;35(6):730–740.
    1. Practice Committee of the American Society for Reproductive M Treatment of pelvic pain associated with endometriosis: a committee opinion. Fertil Steril. 2014;101(4):927–935. doi: 10.1016/j.fertnstert.2014.02.012.
    1. Saraswat L, Ayansina D, Cooper KG, Bhattacharya S, Horne AW, Bhattacharya S. Impact of endometriosis on risk of further gynaecological surgery and cancer: a national cohort study. BJOG. 2018;125(1):64–72. doi: 10.1111/1471-0528.14793.
    1. Lee DY, Kim HJ, Yoon BK, Choi D. Factors associated with the laterality of recurrent endometriomas after conservative surgery. Gynecol Endocrinol. 2013;29(11):978–981. doi: 10.3109/09513590.2013.824959.
    1. Khan KN, Fujishita A, Kitajima M, Hiraki K, Nakashima M, Masuzaki H. Occult microscopic endometriosis: undetectable by laparoscopy in normal peritoneum. Hum Reprod. 2014;29(3):462–472. doi: 10.1093/humrep/det438.
    1. Togashi K, Nishimura K, Kimura I, Tsuda Y, Yamashita K, Shibata T, Nakano Y, Konishi J, Konishi I, Mori T. Endometrial cysts: diagnosis with MR imaging. Radiology. 1991;180(1):73–78. doi: 10.1148/radiology.180.1.2052726.
    1. Vercellini P, Somigliana E, Daguati R, Vigano P, Meroni F, Crosignani PG. Postoperative oral contraceptive exposure and risk of endometrioma recurrence. Am J Obstet Gynecol. 2008;198(5):504 e501–5. doi: 10.1016/j.ajog.2007.11.010.
    1. Adachi K, Takahashi K, Nakamura K, Otake A, Sasamoto N, Miyoshi Y, Shioji M, Yamamoto Y, Fujitani M, Wakimoto A, et al. Postoperative administration of dienogest for suppressing recurrence of disease and relieving pain in subjects with ovarian endometriomas. Gynecol Endocrinol. 2016;32(8):646–649. doi: 10.3109/09513590.2016.1147547.
    1. Lee SR, Yi KW, Song JY, Seo SK, Lee DY, Cho S, Kim SH. Efficacy and safety of long-term use of Dienogest in women with ovarian Endometrioma. Reprod Sci. 2018;25(3):341–346. doi: 10.1177/1933719117725820.
    1. Brinton LA, Gridley G, Persson I, Baron J, Bergqvist A. Cancer risk after a hospital discharge diagnosis of endometriosis. Am J Obstet Gynecol. 1997;176(3):572–579. doi: 10.1016/S0002-9378(97)70550-7.
    1. Melin A, Sparen P, Persson I, Bergqvist A. Endometriosis and the risk of cancer with special emphasis on ovarian cancer. Hum Reprod. 2006;21(5):1237–1242. doi: 10.1093/humrep/dei462.
    1. Kobayashi H, Sumimoto K, Moniwa N, Imai M, Takakura K, Kuromaki T, Morioka E, Arisawa K, Terao T. Risk of developing ovarian cancer among women with ovarian endometrioma: a cohort study in Shizuoka, Japan. Int J Gynecol Cancer. 2007;17(1):37–43. doi: 10.1111/j.1525-1438.2006.00754.x.
    1. Pearce CL, Templeman C, Rossing MA, Lee A, Near AM, Webb PM, Nagle CM, Doherty JA, Cushing-Haugen KL, Wicklund KG, et al. Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case-control studies. Lancet Oncol. 2012;13(4):385–394. doi: 10.1016/S1470-2045(11)70404-1.
    1. Taniguchi F, Harada T, Kobayashi H, Hayashi K, Momoeda M, Terakawa N. Clinical characteristics of patients in Japan with ovarian cancer presumably arising from ovarian endometrioma. Gynecol Obstet Investig. 2014;77(2):104–110. doi: 10.1159/000357819.
    1. Chang WH, Wang KC, Lee WL, Huang N, Chou YJ, Feng RC, Yen MS, Huang BS, Guo CY, Wang PH. Endometriosis and the subsequent risk of epithelial ovarian cancer. Taiwan J Obstet Gynecol. 2014;53(4):530–535. doi: 10.1016/j.tjog.2014.04.025.
    1. Melin AS, Lundholm C, Malki N, Swahn ML, Sparen P, Bergqvist A. Hormonal and surgical treatments for endometriosis and risk of epithelial ovarian cancer. Acta Obstet Gynecol Scand. 2013;92(5):546–554. doi: 10.1111/aogs.12123.
    1. Rossing MA, Cushing-Haugen KL, Wicklund KG, Doherty JA, Weiss NS. Risk of epithelial ovarian cancer in relation to benign ovarian conditions and ovarian surgery. Cancer Causes Control. 2008;19(10):1357–1364. doi: 10.1007/s10552-008-9207-9.
    1. Atsma F, Bartelink ML, Grobbee DE, van der Schouw YT. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause. 2006;13(2):265–279. doi: 10.1097/01.gme.0000218683.97338.ea.
    1. Rocca WA, Grossardt BR, Shuster LT. Oophorectomy, estrogen, and dementia: a 2014 update. Mol Cell Endocrinol. 2014;389(1–2):7–12. doi: 10.1016/j.mce.2014.01.020.
    1. Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ., 3rd Increased risk of parkinsonism in women who underwent oophorectomy before menopause. Neurology. 2008;70(3):200–209. doi: 10.1212/01.wnl.0000280573.30975.6a.
    1. Rosendahl M, Simonsen MK, Kjer JJ. The influence of unilateral oophorectomy on the age of menopause. Climacteric. 2017;20(6):540–544. doi: 10.1080/13697137.2017.1369512.
    1. Bjelland EK, Wilkosz P, Tanbo TG, Eskild A. Is unilateral oophorectomy associated with age at menopause? A population study (the HUNT2 survey) Hum Reprod. 2014;29(4):835–841. doi: 10.1093/humrep/deu026.
    1. Yasui T, Hayashi K, Mizunuma H, Kubota T, Aso T, Matsumura Y, Lee JS, Suzuki S. Factors associated with premature ovarian failure, early menopause and earlier onset of menopause in Japanese women. Maturitas. 2012;72(3):249–255. doi: 10.1016/j.maturitas.2012.04.002.

Source: PubMed

3
Sottoscrivi