Robert's Uterus-Types, Diagnosis, and Management Options: Case Series and Review of Literature.

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This case series and literature review describes Robert's uterus, a rare Mullerian anomaly, and details its types, diagnosis, and management, reporting successful surgical outcomes for three adolescent patients with severe dysmenorrhea.

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This paper reports three adolescent girls with progressive severe dysmenorrhea due to Robert’s uterus, a rare Müllerian anomaly, and describes diagnostic approaches and management options. MRI findings initially suggested juvenile cystic adenomyoma in one case and Robert’s uterus in the other two, and two patients had prior inappropriate surgeries for misdiagnosis that did not relieve symptoms. All three underwent surgery and reported relief from dysmenorrhea, with one receiving laparoscopic blind horn resection and two undergoing ultrasound-guided hysteroscopic septal resection and hematometra drainage; the authors note the need for further long-term follow-up after conservative surgeries. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ObjectiveTo report three cases of Robert's uterus and to describe the types, diagnostic methods, and management options for this rare Mullerian anomaly.MethodsThree adolescent girls presented with progressive severe dysmenorrhea since menarche. Two girls had undergone inappropriate surgeries due to misdiagnosis in past which did not relieve their symptoms. MRI reported as juvenile cystic adenomyoma (JCA) in one girl and Robert's uterus in other two girls.ResultsAll three patients underwent surgical intervention. The first patient underwent laparoscopic blind horn resection and residual myometrial closure. The decision was taken in view of severe symptoms, school dropout, large adenomyotic lesion, and previous one appendicectomy following misdiagnosis, and patient was not willing for any conservative management. The other two patients underwent transabdominal ultrasonography-guided hysteroscopic resection of septum and hematometra drainage. All the patients had relieved from dysmenorrhea and are asymptomatic.ConclusionAll girls presenting with progressive dysmenorrhea should be evaluated for Mullerian anomalies including the rare ones like Robert's uterus. USG-guided hysteroscopic septal resection may be considered for all cases of Robert's uterus for immediate symptom relief and better future reproductive outcomes. Further long-term follow-up of these patients undergoing conservative surgeries is warranted.
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Abstract

Objective To report three cases of Robert’s uterus and to describe the types, diagnostic methods, and management options for this rare Mullerian anomaly.

Methods

Three adolescent girls presented with progressive severe dysmenorrhea since menarche. Two girls had undergone inappropriate surgeries due to misdiagnosis in past which did not relieve their symptoms. MRI reported as juvenile cystic adenomyoma (JCA) in one girl and Robert’s uterus in other two girls.

Results

All three patients underwent surgical intervention. The first patient underwent laparoscopic blind horn resection and residual myometrial closure. The decision was taken in view of severe symptoms, school dropout, large adenomyotic lesion, and previous one appendicectomy following misdiagnosis, and patient was not willing for any conservative management. The other two patients underwent transabdominal ultrasonography-guided hysteroscopic resection of septum and hematometra drainage. All the patients had relieved from dysmenorrhea and are asymptomatic.

Conclusion

All girls presenting with progressive dysmenorrhea should be evaluated for Mullerian anomalies including the rare ones like Robert’s uterus. USG-guided hysteroscopic septal resection may be considered for all cases of Robert’s uterus for immediate symptom relief and better future reproductive outcomes. Further long-term follow-up of these patients undergoing conservative surgeries is warranted. Similar content being viewed by others

References

Mahey R, Cheluvaraju R, Kumari S, et al. Robert’s uterus versus Juvenile cystic adenomyoma-Diagnostic and therapeutic challenges—case report and review of literature. J Hum Reprod Sci. 2023;16:79–86. De A, Jain A, Tripathi R, et al. complete uterine septum with cervical duplication and longitudinal vaginal septum: An anomaly supporting alternative embryological development. J Hum Reprod Sci. 2020;13:352–5. Ludwin A, Ludwin I, Bhagavath B, et al. Pre-, intra-, and postoperative management of Robert’s uterus. Fertil Steril. 2018;110:778–9. Singh S, Malik R, Gupta P, et al. Successful outcome in a perplexing case of Roberts uterus: a rare uterine anomaly, a rare case report with review of literature. Intern J Reprod Contracep Obstet Gynecol. 2020;9(1):440. https://doi.org/10.18203/2320-1770.ijrcog20196064. Romanski PA, Bortoletto P, Pfeifer SM. Unilateral obstructed müllerian anomalies: a series of unusual variants of known anomalies. J Pediatr Adolesc Gynecol. 2021;34:749–57. Kisu I, Nakamura K, Shiraishi T, Iijima T, et al. Inappropriate surgery in a patient with misdiagnosed Robert’s uterus. BMC Womens Health. 2021;21:264. Deenadayal M, Günther V, Alkatout I, et al. Critical role of 3D ultrasound in the diagnosis and management of Robert’s uterus: a single-Centre case series and a review. Facts Views Vis Obgyn. 2021;13:41–9. Shah N, Changede P. Hysteroscopic management of Robert’s uterus. J Obstet Gynaecol India. 2020;70:86–8. Funding None. Author information Authors and Affiliations Corresponding author Ethics declarations Conflict of interest There is conflict of interest among authors. Ethical approval Ethical clearance was taken from the Institutional Ethical committee, Ref No.: IEC-432/17.7.2023. Patient consent statement The patients have consented to share their personal information and images. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Neha Varun is an Associate Professor; Reeta Mahey is a Professor; Archana Kumari is an Associate Professor; Garima Kachhawa is a Professor; Manasi Deoghare is a Senior Resident; Rohitha Cheluvaraju is a DM Reproductive Medicine; Neerja Bhatla is a Professor & Head. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Varun, N., Mahey, R., Kumari, A. et al. Robert’s Uterus-Types, Diagnosis, and Management Options: Case Series and Review of Literature. J Obstet Gynecol India 75 (Suppl 1), 215–220 (2025). https://doi.org/10.1007/s13224-024-02074-5 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s13224-024-02074-5

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