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Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney
BACKGROUND: Unicornuate uterus is a congenital uterine malformation. Unicornuate uterus with rudimentary horn, ovarian endometriosis, and congenital renal agenesis are rare combinations that can be easily misdiagnosed due to the lack of typical clinical manifestations. CASE SUMMARY: A 19-year-old wo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354508/ https://www.ncbi.nlm.nih.gov/pubmed/37476616 http://dx.doi.org/10.3389/fmed.2023.1182355 |
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author | Yin, Si-fan Chai, Jia-gui Feng, Run-lin Yin, Zhi-yuan Zhao, Shen-zhao Zhang, Tao Ke, Chang-xing |
author_facet | Yin, Si-fan Chai, Jia-gui Feng, Run-lin Yin, Zhi-yuan Zhao, Shen-zhao Zhang, Tao Ke, Chang-xing |
author_sort | Yin, Si-fan |
collection | PubMed |
description | BACKGROUND: Unicornuate uterus is a congenital uterine malformation. Unicornuate uterus with rudimentary horn, ovarian endometriosis, and congenital renal agenesis are rare combinations that can be easily misdiagnosed due to the lack of typical clinical manifestations. CASE SUMMARY: A 19-year-old woman with pelvic pain was admitted to the hospital after a month. Physical examination was unremarkable. B-ultrasound and CT scan both indicated pelvic ectopic kidney. In addition, renal scintigraphy revealed normal perfusion and function of the right kidney, but the perfusion and function of the left kidney were not visible. A left pelvic ectopic kidney was diagnosed by preoperative images. A laparoscopic left pelvic ectopic nephrectomy was performed after adequate surgical preparation. However, the postoperative pathological diagnosis revealed a rudimentary uterine horn with ovarian endometriosis and congenital renal agenesis. Fortunately, she got recovered and was discharged from the hospital after 5 days following the operation. Moreover, she received regular follow-ups at the gynecology clinic. To date, no right adnexal or uterine abnormalities have been detected on ultrasound during the follow-up visits. CONCLUSION: Rudimentary uterine horn with ovarian endometriosis and congenital renal agenesis are rare and are easily Misdiagnosed due to the lack of typical clinical manifestations. A gynecological examination is recommended for patients who may have this disease. |
format | Online Article Text |
id | pubmed-10354508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103545082023-07-20 Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney Yin, Si-fan Chai, Jia-gui Feng, Run-lin Yin, Zhi-yuan Zhao, Shen-zhao Zhang, Tao Ke, Chang-xing Front Med (Lausanne) Medicine BACKGROUND: Unicornuate uterus is a congenital uterine malformation. Unicornuate uterus with rudimentary horn, ovarian endometriosis, and congenital renal agenesis are rare combinations that can be easily misdiagnosed due to the lack of typical clinical manifestations. CASE SUMMARY: A 19-year-old woman with pelvic pain was admitted to the hospital after a month. Physical examination was unremarkable. B-ultrasound and CT scan both indicated pelvic ectopic kidney. In addition, renal scintigraphy revealed normal perfusion and function of the right kidney, but the perfusion and function of the left kidney were not visible. A left pelvic ectopic kidney was diagnosed by preoperative images. A laparoscopic left pelvic ectopic nephrectomy was performed after adequate surgical preparation. However, the postoperative pathological diagnosis revealed a rudimentary uterine horn with ovarian endometriosis and congenital renal agenesis. Fortunately, she got recovered and was discharged from the hospital after 5 days following the operation. Moreover, she received regular follow-ups at the gynecology clinic. To date, no right adnexal or uterine abnormalities have been detected on ultrasound during the follow-up visits. CONCLUSION: Rudimentary uterine horn with ovarian endometriosis and congenital renal agenesis are rare and are easily Misdiagnosed due to the lack of typical clinical manifestations. A gynecological examination is recommended for patients who may have this disease. Frontiers Media S.A. 2023-07-05 /pmc/articles/PMC10354508/ /pubmed/37476616 http://dx.doi.org/10.3389/fmed.2023.1182355 Text en Copyright © 2023 Yin, Chai, Feng, Yin, Zhao, Zhang and Ke. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Yin, Si-fan Chai, Jia-gui Feng, Run-lin Yin, Zhi-yuan Zhao, Shen-zhao Zhang, Tao Ke, Chang-xing Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title | Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title_full | Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title_fullStr | Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title_full_unstemmed | Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title_short | Case report: Rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
title_sort | case report: rudimentary uterine horn with ovarian endometriosis manifested as pelvic ectopic kidney |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354508/ https://www.ncbi.nlm.nih.gov/pubmed/37476616 http://dx.doi.org/10.3389/fmed.2023.1182355 |
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