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A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management

Uterine inversion is a rare disease that is particularly uncommon among non-puerperal women. Herein we reported the only case of uterine inversion known to us that was caused by the endometrial thickening and changes in the polypoid lesion in early puberty. The patient was admitted to our hospital b...

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Autores principales: Li, Fang, Liang, Ying, Luo, Mingyan, Cheng, Yufen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932396/
https://www.ncbi.nlm.nih.gov/pubmed/35415248
http://dx.doi.org/10.1515/med-2022-0425
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author Li, Fang
Liang, Ying
Luo, Mingyan
Cheng, Yufen
author_facet Li, Fang
Liang, Ying
Luo, Mingyan
Cheng, Yufen
author_sort Li, Fang
collection PubMed
description Uterine inversion is a rare disease that is particularly uncommon among non-puerperal women. Herein we reported the only case of uterine inversion known to us that was caused by the endometrial thickening and changes in the polypoid lesion in early puberty. The patient was admitted to our hospital because of massive vaginal bleeding, abdominal pain, and a protruding mass from the vagina. We obtained the patient history by collecting the results of various examinations (including magnetic resonance imaging and color Doppler ultrasound), accurate diagnosis was performed, and a reasonable treatment protocol was developed. She was subjected to laparoscopic uterine-sparing surgery to preserve her fertility. Uterine inversion is a rare disease, and early diagnosis and selection of appropriate treatment options are essential for patients with fertility requirements.
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spelling pubmed-89323962022-04-11 A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management Li, Fang Liang, Ying Luo, Mingyan Cheng, Yufen Open Med (Wars) Case Report Uterine inversion is a rare disease that is particularly uncommon among non-puerperal women. Herein we reported the only case of uterine inversion known to us that was caused by the endometrial thickening and changes in the polypoid lesion in early puberty. The patient was admitted to our hospital because of massive vaginal bleeding, abdominal pain, and a protruding mass from the vagina. We obtained the patient history by collecting the results of various examinations (including magnetic resonance imaging and color Doppler ultrasound), accurate diagnosis was performed, and a reasonable treatment protocol was developed. She was subjected to laparoscopic uterine-sparing surgery to preserve her fertility. Uterine inversion is a rare disease, and early diagnosis and selection of appropriate treatment options are essential for patients with fertility requirements. De Gruyter 2022-03-17 /pmc/articles/PMC8932396/ /pubmed/35415248 http://dx.doi.org/10.1515/med-2022-0425 Text en © 2022 Fang Li et al., published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Case Report
Li, Fang
Liang, Ying
Luo, Mingyan
Cheng, Yufen
A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title_full A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title_fullStr A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title_full_unstemmed A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title_short A rare case of endometrial polyp complicated with uterine inversion: A case report and clinical management
title_sort rare case of endometrial polyp complicated with uterine inversion: a case report and clinical management
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932396/
https://www.ncbi.nlm.nih.gov/pubmed/35415248
http://dx.doi.org/10.1515/med-2022-0425
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