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Hysteroscopic presentation of endometrial vascular dystrophy: a case report
Endometrial vascular dystrophy is quite rare, and there is very little literature regarding this subject. We present the unusual case of a 38-year-old woman who experienced vaginal bleeding after menstruation for 3 months. Hysteroscopically, the uterine cavity was filled with tiny, curved blood vess...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134412/ https://www.ncbi.nlm.nih.gov/pubmed/37050885 http://dx.doi.org/10.1177/03000605231166261 |
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author | Jiang, SuZhen Gong, HongXia |
author_facet | Jiang, SuZhen Gong, HongXia |
author_sort | Jiang, SuZhen |
collection | PubMed |
description | Endometrial vascular dystrophy is quite rare, and there is very little literature regarding this subject. We present the unusual case of a 38-year-old woman who experienced vaginal bleeding after menstruation for 3 months. Hysteroscopically, the uterine cavity was filled with tiny, curved blood vessels, the bottom of the cavity was obvious, and polyps were visible. No curved vessels or polyps were identified after curettage. The diagnosis was endometrial hemodystrophy with endometrial polyps. Endometrial vascular dystrophy is a hysteroscopically uncommon benign lesion of the endometrial vessels. |
format | Online Article Text |
id | pubmed-10134412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-101344122023-04-28 Hysteroscopic presentation of endometrial vascular dystrophy: a case report Jiang, SuZhen Gong, HongXia J Int Med Res Case Reports Endometrial vascular dystrophy is quite rare, and there is very little literature regarding this subject. We present the unusual case of a 38-year-old woman who experienced vaginal bleeding after menstruation for 3 months. Hysteroscopically, the uterine cavity was filled with tiny, curved blood vessels, the bottom of the cavity was obvious, and polyps were visible. No curved vessels or polyps were identified after curettage. The diagnosis was endometrial hemodystrophy with endometrial polyps. Endometrial vascular dystrophy is a hysteroscopically uncommon benign lesion of the endometrial vessels. SAGE Publications 2023-04-12 /pmc/articles/PMC10134412/ /pubmed/37050885 http://dx.doi.org/10.1177/03000605231166261 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Jiang, SuZhen Gong, HongXia Hysteroscopic presentation of endometrial vascular dystrophy: a case report |
title | Hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
title_full | Hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
title_fullStr | Hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
title_full_unstemmed | Hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
title_short | Hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
title_sort | hysteroscopic presentation of endometrial vascular dystrophy: a case
report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134412/ https://www.ncbi.nlm.nih.gov/pubmed/37050885 http://dx.doi.org/10.1177/03000605231166261 |
work_keys_str_mv | AT jiangsuzhen hysteroscopicpresentationofendometrialvasculardystrophyacasereport AT gonghongxia hysteroscopicpresentationofendometrialvasculardystrophyacasereport |