Skip to main content

Contralateral ovarian endometrioma recurrence after unilateral salpingo-oophorectomy

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.

Peer Review reports

Background

Endometriosis is a chronic inflammatory disease caused by the development of tissues resembling endometrium outside the uterus, mainly in the ovary, uterosacral ligament, and pelvic peritoneum [1,2,3]. Endometriosis affects approximately 10% of women in their reproductive years and is associated with dysmenorrhea, pelvic pain, and infertility. Ovarian endometriomas are reportedly present in 17–44% of endometriosis cases [4]. Laparoscopic surgery should be considered for patients who require pain relief, cyst removal, or histological diagnosis, although the risk of diminishing ovarian reserve should also be considered [1].

Typically, conservative surgery is preferred over radical procedures because most patients with endometrioma are of the reproductive age [5]. However, a systematic literature review estimated the 2- and 5-year endometriosis recurrence rates after conservative surgery as 21.5% and 40–50%, respectively [6]. Furthermore, the recurrence rate after a second surgery may be comparable to that after the first conservative surgery for endometrioma [7]. Oophorectomy is sometimes performed as a semi-radical surgery when the ovarian cyst is large, multiloculated, or potentially malignant. Unilateral oophorectomy may be well-suited as a radical treatment for unilateral ovarian endometrioma in women who do not plan to conceive in the future with the expectation that the risk of postoperative recurrence will be reduced. According to the largest study on the incidence of premenopausal unilateral oophorectomy, 295/1838 (20.1%) patients who underwent the procedure for a medical indication were pathologically diagnosed with endometriosis [8].

However, there are no reports on the disease recurrence rate after USO for unilateral endometrioma. Therefore, we investigated the rate of and risk factors for disease recurrence after USO for unilateral ovarian endometrioma. To our knowledge, this is the first report on the recurrence rate and risk factors associated with recurrence after USO.

Methods

We performed a retrospective study of patients aged 35–45 years who underwent laparoscopic USO or laparoscopic cystectomy for an MRI-confirmed unilateral ovarian endometrioma at the University of Tokyo Hospital between 2010 and 2012.

The inclusion criteria were: age between 35 and 45 years, and preoperative magnetic resonance imaging (MRI)-confirmed unilateral ovarian endometrioma. The exclusion criteria were: the presence of bilateral endometriomas at study enrollment, previous unilateral or bilateral oophorectomy, and pathological diagnosis of malignancy.

We enrolled 110 patients after reviewing the medical records. We recorded the patient age at the time of the operation; history of pregnancy, parturition, dysmenorrhea, and infertility; diameter of the largest cyst; the presence of multilocular cysts, uterine fibroids, and adenomyosis; the revised American Society for Reproductive Medicine (r-ASRM) [9] classification score; r-ASRM ipsilateral and contralateral side adhesion scores; and postoperative hormonal therapy, pregnancy, delivery, follow-up length, and recurrence. According to the r-ASRM score system, the right and left ovary and fallopian tube adhesion scores were summed separately, and we defined the ovarian endometrioma side as ipsilateral. A unilateral ovarian endometrioma was confirmed in all patients by preoperative 3.0 Tesla MRI. One day prior to surgery, transvaginal ultrasound confirmed the presence of endometrioma and the absence of endometrioma on the contralateral side in all cases. Patients were divided into the USO and cystectomy groups after reviewing and comparing medical records. The Institutional Review Board of Tokyo University Hospital approved the study. All patients provided written informed consent to participate in the research before surgery.

Surgery

Laparoscopic surgery for ovarian endometrioma began with an inspection of the pelvis and ovarian adhesiolysis.

Laparoscopic USO continued with isolation, coagulation, and division of the ovarian artery and vein. The pelvic peritoneal incision was extended toward the ovarian ligament, and the oviduct and ovarian ligament were coagulated and divided using bipolar electrocoagulation. Upon completion of USO, bipolar electrocoagulation was used to obtain hemostasis. Alternatively, laparoscopic ovarian cystectomy continued with a sharp cortical incision and identification of a cleavage plane as previously described [10, 11]. The cyst capsule was completely stripped from the ovarian tissue using appropriate traction and sharp dissection.

In both procedures, all endometriotic peritoneal implants were excised with scissors or coagulated with bipolar electrocoagulation. The surgeon also inspected the contralateral ovary and fallopian tube and performed adhesiolysis as required. Coagulation was used to obtain hemostasis after adhesiolysis. The surgeons assigned r-ASRM scores according to the intraoperative findings [9]. We retrospectively reviewed the surgical records, including r-ASRM scores, of all patients.

Definition of recurrent ovarian endometrioma

All patients were instructed to undergo transvaginal ultrasound monitoring for recurrence every 3 months postoperatively. We defined endometrioma recurrence as in our previous studies [10,11,12]. Briefly, recurrence was defined as the presence of an ovarian cyst (> 2 cm) with typical features of an endometrioma identified on ultrasound [13]. A diagnosis of recurrence was made when the cyst was repeatedly observed with ultrasonography or MRI.

Statistical analysis

We used JMP Pro 14 software (SAS Institute Inc., Cary, NC, US) for all statistical analyses. Continuous data were analyzed with t-tests and are presented as means and standard deviations (SDs). Categorial data were analyzed with chi-square and Fisher’s exact tests and are presented as counts and percentages. Univariate and multivariate stepwise logistic regression analyses were performed to compare the clinical characteristics of patients with and without ovarian endometrioma recurrence. The Kaplan-Meier method and log-rank test were used to compare the postoperative cumulative recurrence rates. A P-value of < 0.05 was considered statistically significant.

Results

Patient and case characteristics

The demographic variables, intraoperative findings, and postoperative course of all 110 patients with unilateral ovarian endometrioma are shown in Table 1. Compared to the cystectomy group, patients in the USO group were older at the time of surgery; there were also more preoperative pregnancies and births, as well as fewer infertile patients in the USO group. The r-ASRM and ipsilateral side adhesion scores were significantly higher in the USO group than in the cystectomy group.

Table 1 Characteristics of patients who underwent USO or cystectomy for unilateral ovarian endometrioma

Postoperative hormonal therapy was administered in 10/50 cases after USO and 24/60 cases after cystectomy (20.0% vs. 41.7%, P = 0.0375). Postoperative fertility treatment, pregnancy, and delivery were also less frequent in the USO group than in the cystectomy group. Endometrioma recurrence occurred in 8 (16.0%) and 7 (11.7%) patients in the USO and cystectomy groups, respectively.

Characteristics of patients with and without recurrence after USO

Table 2 shows the characteristics of cases with and without post-USO recurrence. In univariate analysis, the frequency of patients with a contralateral side adhesion score ≥ 4 was significantly higher in the recurrence group than in the non-recurrence group. The postoperative follow-up period was significantly longer in patients with than in those without a recurrence. We identified largest cyst diameter, r-ASRM score, ipsilateral side adhesion score ≥ 16, and contralateral side adhesion score ≥ 4 as factors for logistic regression analysis using forward stepwise variable selection. Of these, only a contralateral side adhesion score ≥ 4 was independently associated with recurrence (P = 0.020; OR, 19.48; 95% CI, 1.59–237.72). Douglas pouch obliteration and r-ASRM score were not associated with the recurrence rate.

Table 2 Univariate and logistic regression analysis of factors related recurrence after USO for unilateral ovarian endometrioma

The cumulative recurrence rates by Kaplan-Meier analysis at 12, 24, 36, and 57 months postoperatively were 19.5, 24.1, 31.0, and 54.0%, respectively, in cases with an adhesion score ≥ 4, and 0.0, 0.0, 0.0, and 5.9%, respectively, in cases with an adhesion score < 4 (Fig. 1). Our comparison of cumulative recurrence rates revealed that the recurrence rate was significantly higher in cases with adhesion score ≥ 4 than in those with an adhesion score < 4 (P = 0.0023, log-rank analysis).

Fig. 1
figure 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 < 4 (P = 0.0023, log-rank test)

The cumulative recurrence rates by Kaplan-Meier analysis at 12, 24, 36, and 60 months postoperatively were 10.0, 10.0, 10.0, and 10.0%, respectively, in cases with postoperative hormonal therapy, and 7.5, 10.3, 13.6, and 27.3% in cases without postoperative hormonal therapy; this difference was not significant. The only case of endometrioma recurrence in the hormonal therapy group (Table 2) occurred in a patient who received low-dose dienogest (1 mg/day). After increasing her dienogest to the standard dose (2 mg/day), the size of the recurrent cyst decreased to less than 2 cm.

Discussion

In this study of USO and conservative surgery performed for MRI-confirmed unilateral endometrioma, age, history of pregnancy, r-ASRM score, and the frequency of postoperative fertility treatment and hormonal therapy were different between patients who underwent USO and those who underwent cystectomy. Eight out of 50 patients who underwent USO for unilateral ovarian endometrioma had recurrence of endometrioma on the contralateral side. Univariate and logistic regression analyses of characteristics in groups with and without recurrence after USO revealed that a contralateral adhesion score ≥ 4 was a significant risk factor for endometrioma recurrence. Furthermore, there was a significant difference in the cumulative recurrence rate in patients with and without a contralateral side adhesion score ≥ 4. To our knowledge, this is the first study to evaluate the endometrioma recurrence rate and identify recurrence risk factors after USO for unilateral endometrioma.

Endometriosis is a chronic inflammatory disease that recurs after surgery and requires the maximum use of medical treatment to avoid repeated surgeries [14]. Patients diagnosed with endometriosis were reported to have a high risk of further surgery [15]. Although there is no report on recurrence rate after USO for unilateral ovarian endometrioma, we do encounter recurrent cases. Even after conservative surgery, the rates of recurrence of endometriosis on the ipsilateral and contralateral sides are reportedly similar [16]. Additionally, one study identified microscopic endometriosis, a phenomenon that could cause recurrence even after successful surgery [17]. Consequently, it is not surprising that endometriosis recurs on the contralateral side after USO.

With regard to patients’ background, age, parity, and the frequency of postoperative fertility treatment and pregnancy, there was significant difference between the USO and cystectomy groups, possibly because we did not offer USO to patients who wish to conceive. In addition, r-ASRM score and frequency of Douglas pouch obliteration were also significantly higher in the USO group, indicating that it was more severe compared to the cystectomy group. Furthermore, fewer USO group patients received postoperative hormonal treatment, which may have been withheld by clinicians under the impression that the post-USO recurrence rate is low due to the radical nature of the procedure, withheld such therapy. Since the patient backgrounds were widely varied, comparing the postoperative recurrence rates between the USO and cystectomy groups was inappropriate; however, on average, 16% in the USO group have relapsed in the postoperative follow-up period of 46 months; this indicates that the risk of postoperative recurrence also needs to be taken into account with USO.

Here, a contralateral side adhesion score ≥ 4 was identified as a recurrence risk factor after USO. However, we found no difference in the contralateral adhesion scores in cases with and without recurrence, and a contralateral adhesion score ≥ 16 was not a recurrence risk factor. Thus, while the presence of contralateral adhesions was significantly related to recurrence after USO, the severity of the adhesions was not. Regardless of the severity of adhesions, the fact that adhesion is formed itself is evidence that endometriosis extends to the contralateral side, and microscopic endometriosis may cause recurrence even after successful operation [17]. Therefore, we propose that the risk of recurrence should not be underestimated, even in patients with mild adhesions on the contralateral side.

In this study, all patients underwent preoperative MRI and received a transvaginal ultrasonography just prior to surgery, which confirmed the presence of a unilateral ovarian endometrioma and the absence of a contralateral endometrioma. In particular, MRI is the most powerful imaging technique in the diagnosis of ovarian endometrioma, with high sensitivity (90%), specificity (98%), and accuracy (96%) [18]. Therefore, patients in our study were unlikely to have a preoperatively undetected contralateral ovarian endometrioma.

We found no significant difference in recurrence rates with or without postoperative hormonal therapy. However, the sole case of recurrence in the hormonal therapy group might have occurred because the patient was receiving an inappropriate dienogest dose (half the usual dose). Indeed, when dienogest was increased to the standard dose, the recurrent cyst decreased in size. Furthermore, reports indicate that oral contraceptive [5, 11, 19] and dienogest [20, 21] administration lowered the endometrioma recurrence rate after conservative surgery. Thus, it seems theoretically possible that postoperative hormonal therapy could reduce the post-USO recurrence rate as well. Therefore, in cases of endometrioma accompanied by contralateral side adhesions, we propose prescribing postoperative hormonal therapy after USO.

Endometriosis is reportedly an ovarian cancer risk factor [3, 22,23,24,25]. Notably, ovarian endometrioma was implicated as a putative precursor lesion of endometrioid and clear cell ovarian cancer, and risk-reducing surgery has been recommended [3, 25]. Studies indicate that cystectomy does not reduce the risk of malignant transformation or ovarian cancer [26, 27]; however, the frequency of malignant transformation declined after USO [28, 29]. Therefore, USO could be an option that reduces the risk of malignant transformation.

Surgical menopause caused by bilateral salpingo-oophorectomy (BSO) has been correlated with an increased risk of cardiovascular disease, [30] dementia, [31] and Parkinsonism [32]. Furthermore, premenopausal USO reportedly reduces the age of menopause by 1.2 to 1.8 years, [33,34,35] although many, assuming that the remaining ovary compensates for the removed ovary, believe that USO is safer than BSO. However, whether USO affects the risk of cardiovascular events, dementia, and other diseases remains unknown. Future studies of USO and cystectomy outcomes are necessary to obtain evidence about postoperative recurrence rates, fertility preservation, surgical menopause, and potential for subsequent malignant transformation.

This study has several limitations. First, we performed a single-institution retrospective study; Therefore, our results require confirmation at other facilities. Second, patient characteristics differed between the USO and cystectomy groups, which could have caused bias. Therefore, in this study, we could not compare the recurrence rate between both groups. Third, we did not evaluate the recurrence of pain (e.g., dysmenorrhea and chronic pelvic pain), which is an important consideration when evaluating the effect of surgery in patients with endometriosis. A large-scale prospective study is required to overcome these limitations.

Conclusion

To our knowledge, this is the first report on the recurrence rate and risk factors associated with recurrence after USO. In particular, the recurrence rate significantly increased in the presence of contralateral side adhesions. Thus, clinicians should be aware of the recurrence of endometriosis, even after USO, especially if contralateral adhesions are present. Our findings could improve the planning of USO and selection of patients for postoperative hormonal therapy.

Abbreviations

BSO:

Bilateral salpingo-oophorectomy

MRI:

Magnetic resonance imaging

r-ASRM score:

the revised American Society for Reproductive Medicine score

USO:

Unilateral salpingo-oophorectomy

References

  1. Zondervan KT, Becker CM, Koga K, Missmer SA, Taylor RN, Vigano P. Endometriosis. Nat Rev Dis Primers. 2018;4(1):9.

    Article  PubMed  Google Scholar 

  2. Giudice LC, Kao LC. Endometriosis. Lancet. 2004;364(9447):1789–99.

    Article  PubMed  Google Scholar 

  3. Vercellini P, Vigano P, Somigliana E, Fedele L. Endometriosis: pathogenesis and treatment. Nat Rev Endocrinol. 2014;10(5):261–75.

    Article  CAS  PubMed  Google Scholar 

  4. Chapron C, Vercellini P, Barakat H, Vieira M, Dubuisson JB. Management of ovarian endometriomas. Hum Reprod Update. 2002;8(6):591–7.

    Article  CAS  PubMed  Google Scholar 

  5. 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.

    Article  PubMed  Google Scholar 

  6. Guo SW. Recurrence of endometriosis and its control. Hum Reprod Update. 2009;15(4):441–61.

    Article  PubMed  Google Scholar 

  7. 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 e211–6.

    Article  Google Scholar 

  8. 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):442–9.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Revised American Society for Reproductive Medicine classification of endometriosis: 1996. Fertil Steril. 1997;67(5):817–821.

  10. 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):2171–4.

    Article  CAS  PubMed  Google Scholar 

  11. 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):3042–8.

    Article  CAS  PubMed  Google Scholar 

  12. 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.

    Article  PubMed  Google Scholar 

  13. 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):730–40.

    PubMed  Google Scholar 

  14. Practice Committee of the American Society for Reproductive M. Treatment of pelvic pain associated with endometriosis: a committee opinion. Fertil Steril. 2014;101(4):927–35.

    Article  Google Scholar 

  15. 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.

    Article  CAS  PubMed  Google Scholar 

  16. Lee DY, Kim HJ, Yoon BK, Choi D. Factors associated with the laterality of recurrent endometriomas after conservative surgery. Gynecol Endocrinol. 2013;29(11):978–81.

    Article  PubMed  Google Scholar 

  17. 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):462–72.

    Article  PubMed  Google Scholar 

  18. 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):73–8.

    Article  CAS  PubMed  Google Scholar 

  19. 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.

    Article  Google Scholar 

  20. 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):646–9.

    Article  CAS  PubMed  Google Scholar 

  21. 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):341–6.

    Article  CAS  PubMed  Google Scholar 

  22. 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):572–9.

    Article  CAS  PubMed  Google Scholar 

  23. 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):1237–42.

    Article  CAS  PubMed  Google Scholar 

  24. 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.

    Article  CAS  PubMed  Google Scholar 

  25. 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):385–94.

    Article  PubMed  PubMed Central  Google Scholar 

  26. 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):104–10.

    Article  Google Scholar 

  27. 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):530–5.

    Article  PubMed  Google Scholar 

  28. 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):546–54.

    Article  PubMed  Google Scholar 

  29. 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):1357–64.

    Article  PubMed  PubMed Central  Google Scholar 

  30. 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):265–79.

    Article  PubMed  Google Scholar 

  31. Rocca WA, Grossardt BR, Shuster LT. Oophorectomy, estrogen, and dementia: a 2014 update. Mol Cell Endocrinol. 2014;389(1–2):7–12.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. 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):200–9.

    Article  CAS  PubMed  Google Scholar 

  33. Rosendahl M, Simonsen MK, Kjer JJ. The influence of unilateral oophorectomy on the age of menopause. Climacteric. 2017;20(6):540–4.

    Article  CAS  PubMed  Google Scholar 

  34. 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):835–41.

    Article  CAS  PubMed  Google Scholar 

  35. 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):249–55.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

We would like to thank Editage (www.editage.jp) for the English language review.

Funding

This work was supported by grants from the Japanese Ministry of Health, Labour and Welfare; the Japanese Ministry of Education, Culture, Sports, Science and Technology; and the Japan Agency for Medical Research and Development.

Availability of data and materials

The datasets used and analyzed during this study are available from the corresponding author on reasonable request.

Author information

Authors and Affiliations

Authors

Contributions

ToH performed the study and was a major contributor in writing the manuscript. TeH designed and performed the study, and was a major contributor in analyzing and interpreting data, writing the manuscript, and providing final approval of the final version to be submitted. TA, KN, SF, AN, NN, SM and HS were substantial contributors in acquisition of clinical data. KK, MT, MH, YH, OW, and TF participated in the study design, and provided feedback on the manuscript. YO supervised this study, interpreted data, and provided final approval of the version to be submitted. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Tetsuya Hirata.

Ethics declarations

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.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hidari, T., Hirata, T., Arakawa, T. et al. Contralateral ovarian endometrioma recurrence after unilateral salpingo-oophorectomy. BMC Women's Health 19, 59 (2019). https://doi.org/10.1186/s12905-019-0760-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12905-019-0760-z

Keywords