Cargando…
Cervical adenofibroma without clinical symptoms: report of a rare case
Adenofibroma is an extremely rare benign biphasic tumour composed of glandular and fibrous tissues. It occurs more often in the endometrium but it can also occur in the cervix and extrauterine sites. This case report describes a 39-year-old asymptomatic woman with cervical adenofibroma. The patient...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523848/ https://www.ncbi.nlm.nih.gov/pubmed/36168707 http://dx.doi.org/10.1177/03000605221125525 |
_version_ | 1784800377646874624 |
---|---|
author | Li, Bing-Bing Zheng, Yi-Hong Chen, Qiu-Yan Guo, Zhen-Qiang |
author_facet | Li, Bing-Bing Zheng, Yi-Hong Chen, Qiu-Yan Guo, Zhen-Qiang |
author_sort | Li, Bing-Bing |
collection | PubMed |
description | Adenofibroma is an extremely rare benign biphasic tumour composed of glandular and fibrous tissues. It occurs more often in the endometrium but it can also occur in the cervix and extrauterine sites. This case report describes a 39-year-old asymptomatic woman with cervical adenofibroma. The patient was treated successfully with surgical removal of the tumour. As adenofibromas are very rare, the report is presented with a brief review of the literature. |
format | Online Article Text |
id | pubmed-9523848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-95238482022-10-01 Cervical adenofibroma without clinical symptoms: report of a rare case Li, Bing-Bing Zheng, Yi-Hong Chen, Qiu-Yan Guo, Zhen-Qiang J Int Med Res Case Reports Adenofibroma is an extremely rare benign biphasic tumour composed of glandular and fibrous tissues. It occurs more often in the endometrium but it can also occur in the cervix and extrauterine sites. This case report describes a 39-year-old asymptomatic woman with cervical adenofibroma. The patient was treated successfully with surgical removal of the tumour. As adenofibromas are very rare, the report is presented with a brief review of the literature. SAGE Publications 2022-09-27 /pmc/articles/PMC9523848/ /pubmed/36168707 http://dx.doi.org/10.1177/03000605221125525 Text en © The Author(s) 2022 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 Li, Bing-Bing Zheng, Yi-Hong Chen, Qiu-Yan Guo, Zhen-Qiang Cervical adenofibroma without clinical symptoms: report of a rare case |
title | Cervical adenofibroma without clinical symptoms: report of a rare case |
title_full | Cervical adenofibroma without clinical symptoms: report of a rare case |
title_fullStr | Cervical adenofibroma without clinical symptoms: report of a rare case |
title_full_unstemmed | Cervical adenofibroma without clinical symptoms: report of a rare case |
title_short | Cervical adenofibroma without clinical symptoms: report of a rare case |
title_sort | cervical adenofibroma without clinical symptoms: report of a rare case |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523848/ https://www.ncbi.nlm.nih.gov/pubmed/36168707 http://dx.doi.org/10.1177/03000605221125525 |
work_keys_str_mv | AT libingbing cervicaladenofibromawithoutclinicalsymptomsreportofararecase AT zhengyihong cervicaladenofibromawithoutclinicalsymptomsreportofararecase AT chenqiuyan cervicaladenofibromawithoutclinicalsymptomsreportofararecase AT guozhenqiang cervicaladenofibromawithoutclinicalsymptomsreportofararecase |