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Inappropriate surgery in a patient with misdiagnosed Robert’s uterus

Background Robert’s uterus is a rare Mullerian anomaly, which can be described as an asymmetric, septate uterus with a non-communicating hemicavity. Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive and disadvantageous surgery. Case presentation A 16-year-old wo...

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Published in:BMC women's health 2021-07, Vol.21 (1), p.1-264, Article 264
Main Authors: Kisu, Iori, Nakamura, Kanako, Shiraishi, Tetsuro, Iijima, Tomoko, Iijima, Moito, Matsuda, Kiyoko, Hirao, Nobumaru
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cited_by cdi_FETCH-LOGICAL-c473t-5844ce3617bfb5bf9ff5fbeb88f44ba5eb3cb7316b60c7441be01ee54057c34d3
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container_title BMC women's health
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Nakamura, Kanako
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Iijima, Tomoko
Iijima, Moito
Matsuda, Kiyoko
Hirao, Nobumaru
description Background Robert’s uterus is a rare Mullerian anomaly, which can be described as an asymmetric, septate uterus with a non-communicating hemicavity. Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive and disadvantageous surgery. Case presentation A 16-year-old woman was referred to our department because of dysmenorrhea and suspicion of uterine malformation. We misdiagnosed Robert’s uterus as a unicornuate uterus with a non-communicating rudimentary horn and hematometra, and performed laparoscopic hemi-hysterectomy. Although the patient’s symptoms were relieved, our surgical procedure left the lateral uterine wall weak, making the patient’s uterus susceptible to uterine rupture in any future pregnancy. Conclusions Although the early diagnosis of Robert’s uterus is challenging, it is important in order to determine appropriate surgical interventions and management for maintaining the quality of life and ensuring safety in future pregnancies.
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Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive and disadvantageous surgery. Case presentation A 16-year-old woman was referred to our department because of dysmenorrhea and suspicion of uterine malformation. We misdiagnosed Robert’s uterus as a unicornuate uterus with a non-communicating rudimentary horn and hematometra, and performed laparoscopic hemi-hysterectomy. Although the patient’s symptoms were relieved, our surgical procedure left the lateral uterine wall weak, making the patient’s uterus susceptible to uterine rupture in any future pregnancy. Conclusions Although the early diagnosis of Robert’s uterus is challenging, it is important in order to determine appropriate surgical interventions and management for maintaining the quality of life and ensuring safety in future pregnancies.</description><identifier>ISSN: 1472-6874</identifier><identifier>EISSN: 1472-6874</identifier><identifier>DOI: 10.1186/s12905-021-01404-3</identifier><identifier>PMID: 34217289</identifier><language>eng</language><publisher>London: BioMed Central</publisher><subject>Abdomen ; Asymmetry ; Case Report ; Case reports ; Cervix ; Congenital diseases ; Disease ; Dysmenorrhea ; Endometrium ; Infertility ; Laparoscopy ; Magnetic resonance imaging ; Menstruation ; Mullerian anomaly ; Pain ; Quality of life ; Robert’s uterus ; Rudimentary horn ; Septate uterus ; Surgery ; Unicornuate uterus ; Uterus ; Womens health</subject><ispartof>BMC women's health, 2021-07, Vol.21 (1), p.1-264, Article 264</ispartof><rights>2021. 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Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive and disadvantageous surgery. Case presentation A 16-year-old woman was referred to our department because of dysmenorrhea and suspicion of uterine malformation. We misdiagnosed Robert’s uterus as a unicornuate uterus with a non-communicating rudimentary horn and hematometra, and performed laparoscopic hemi-hysterectomy. Although the patient’s symptoms were relieved, our surgical procedure left the lateral uterine wall weak, making the patient’s uterus susceptible to uterine rupture in any future pregnancy. 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Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive and disadvantageous surgery. Case presentation A 16-year-old woman was referred to our department because of dysmenorrhea and suspicion of uterine malformation. We misdiagnosed Robert’s uterus as a unicornuate uterus with a non-communicating rudimentary horn and hematometra, and performed laparoscopic hemi-hysterectomy. Although the patient’s symptoms were relieved, our surgical procedure left the lateral uterine wall weak, making the patient’s uterus susceptible to uterine rupture in any future pregnancy. 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subjects Abdomen
Asymmetry
Case Report
Case reports
Cervix
Congenital diseases
Disease
Dysmenorrhea
Endometrium
Infertility
Laparoscopy
Magnetic resonance imaging
Menstruation
Mullerian anomaly
Pain
Quality of life
Robert’s uterus
Rudimentary horn
Septate uterus
Surgery
Unicornuate uterus
Uterus
Womens health
title Inappropriate surgery in a patient with misdiagnosed Robert’s uterus
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