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Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review

BACKGROUND: Robert’s uterus is a rare congenital anomaly, characterized as an asymmetric septate uterus that has a blind hemicavity with unilateral menstrual fluid retention and a unicornuate hemicavity connecting to the cervix unimpededly. Patients with Robert’s uterus generally present with menstr...

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Autores principales: Dong, Lingling, Qin, Shi, Che, Ronghua, Pei, Jindan, Hua, Xiaolin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044360/
https://www.ncbi.nlm.nih.gov/pubmed/36978042
http://dx.doi.org/10.1186/s12884-023-05541-5
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author Dong, Lingling
Qin, Shi
Che, Ronghua
Pei, Jindan
Hua, Xiaolin
author_facet Dong, Lingling
Qin, Shi
Che, Ronghua
Pei, Jindan
Hua, Xiaolin
author_sort Dong, Lingling
collection PubMed
description BACKGROUND: Robert’s uterus is a rare congenital anomaly, characterized as an asymmetric septate uterus that has a blind hemicavity with unilateral menstrual fluid retention and a unicornuate hemicavity connecting to the cervix unimpededly. Patients with Robert’s uterus generally present with menstrual disorders and dysmenorrhea, and some may have reproductive problems as well, including infertility, recurrent miscarriage, preterm labor and obstetric complications. In this case, we describe a successful pregnancy implanted on the obstructed hemicavity and delivered a liveborn girl. Meanwhile, we highlight diagnostic and therapeutic difficulties in patients with atypical symptoms of Robert’s uterus. CASE PRESENTATION: A 30-year-old Chinese primigravida sought for emergency treatment at 26 weeks and 2 days of gestation because of preterm premature rupture of membranes (PPROM). At the age of 19, the patient was misdiagnosed with hyperprolactinemia and pituitary microadenoma for showing symptom of hypomenorrhea and was suspected to have a uterine septum in the first trimester. She was diagnosed with Robert’s uterus at 22 weeks of gestation by repetitious prenatal transvaginal ultrasonography, which was subsequently confirmed by magnetic resonance imaging. At 26 weeks and 3 days of gestation, the patient was suspected to have oligohydramnion, irregular uterine contraction, and umbilical cord prolapse, and she expressed a strong will of saving the baby. Emergency cesarean delivery was performed and a small hole, together with several weak spots, was found at the lower and back wall of the septum of the patient. The treatment was effective and both the mother and the infant, who had an extremely low birth weight, were discharged in good health conditions. CONCLUSIONS: Pregnancy in the blind cavity of Robert's uterus with living neonates is incredibly rare. In our case, the favorable outcome may result from the unusual hole found at the septum, which may play a role in communicating amniotic fluid between the two hemicavities so to keep the neonate alive. we highlight the importance of early diagnosis and pre-pregnancy treatment of this uterine malformation, and the timely termination of pregnancy, for improving birth quality and reducing mortality.
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spelling pubmed-100443602023-03-29 Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review Dong, Lingling Qin, Shi Che, Ronghua Pei, Jindan Hua, Xiaolin BMC Pregnancy Childbirth Case Report BACKGROUND: Robert’s uterus is a rare congenital anomaly, characterized as an asymmetric septate uterus that has a blind hemicavity with unilateral menstrual fluid retention and a unicornuate hemicavity connecting to the cervix unimpededly. Patients with Robert’s uterus generally present with menstrual disorders and dysmenorrhea, and some may have reproductive problems as well, including infertility, recurrent miscarriage, preterm labor and obstetric complications. In this case, we describe a successful pregnancy implanted on the obstructed hemicavity and delivered a liveborn girl. Meanwhile, we highlight diagnostic and therapeutic difficulties in patients with atypical symptoms of Robert’s uterus. CASE PRESENTATION: A 30-year-old Chinese primigravida sought for emergency treatment at 26 weeks and 2 days of gestation because of preterm premature rupture of membranes (PPROM). At the age of 19, the patient was misdiagnosed with hyperprolactinemia and pituitary microadenoma for showing symptom of hypomenorrhea and was suspected to have a uterine septum in the first trimester. She was diagnosed with Robert’s uterus at 22 weeks of gestation by repetitious prenatal transvaginal ultrasonography, which was subsequently confirmed by magnetic resonance imaging. At 26 weeks and 3 days of gestation, the patient was suspected to have oligohydramnion, irregular uterine contraction, and umbilical cord prolapse, and she expressed a strong will of saving the baby. Emergency cesarean delivery was performed and a small hole, together with several weak spots, was found at the lower and back wall of the septum of the patient. The treatment was effective and both the mother and the infant, who had an extremely low birth weight, were discharged in good health conditions. CONCLUSIONS: Pregnancy in the blind cavity of Robert's uterus with living neonates is incredibly rare. In our case, the favorable outcome may result from the unusual hole found at the septum, which may play a role in communicating amniotic fluid between the two hemicavities so to keep the neonate alive. we highlight the importance of early diagnosis and pre-pregnancy treatment of this uterine malformation, and the timely termination of pregnancy, for improving birth quality and reducing mortality. BioMed Central 2023-03-28 /pmc/articles/PMC10044360/ /pubmed/36978042 http://dx.doi.org/10.1186/s12884-023-05541-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Dong, Lingling
Qin, Shi
Che, Ronghua
Pei, Jindan
Hua, Xiaolin
Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title_full Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title_fullStr Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title_full_unstemmed Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title_short Successful pregnancy in the blind hemicavity of Robert’s uterus: a rare case report and brief literature review
title_sort successful pregnancy in the blind hemicavity of robert’s uterus: a rare case report and brief literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044360/
https://www.ncbi.nlm.nih.gov/pubmed/36978042
http://dx.doi.org/10.1186/s12884-023-05541-5
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