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Intravenous leiomyomatosis: A case study and literature review()
The dissertation presents a case of intravenous leiomyomatosis and conducts the literature review. A 31-year-old woman with a hysteromyomectomy history presented with abnormal uterine bleeding and anemia, a large pelvic tumor, underwent excision of the uterine and bilateral salpingo-oophorectomy. A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464787/ https://www.ncbi.nlm.nih.gov/pubmed/36105826 http://dx.doi.org/10.1016/j.radcr.2022.08.020 |
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author | Lan, Suwei Wang, Xingcha Li, Yang Zhai, Mingjing |
author_facet | Lan, Suwei Wang, Xingcha Li, Yang Zhai, Mingjing |
author_sort | Lan, Suwei |
collection | PubMed |
description | The dissertation presents a case of intravenous leiomyomatosis and conducts the literature review. A 31-year-old woman with a hysteromyomectomy history presented with abnormal uterine bleeding and anemia, a large pelvic tumor, underwent excision of the uterine and bilateral salpingo-oophorectomy. A pathological diagnosis determined it as intravenous leiomyomatosis. The patient recovered well, and no recurrence was noted after 1 year of follow-up. Intravenous leiomyomatosis is rare. Imaging is helpful, but the final diagnosis of intravenous leiomyomatosis is usually made following surgical excision and histopathology. Early surgical resection is a better treatment modality. |
format | Online Article Text |
id | pubmed-9464787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94647872022-09-13 Intravenous leiomyomatosis: A case study and literature review() Lan, Suwei Wang, Xingcha Li, Yang Zhai, Mingjing Radiol Case Rep Case Report The dissertation presents a case of intravenous leiomyomatosis and conducts the literature review. A 31-year-old woman with a hysteromyomectomy history presented with abnormal uterine bleeding and anemia, a large pelvic tumor, underwent excision of the uterine and bilateral salpingo-oophorectomy. A pathological diagnosis determined it as intravenous leiomyomatosis. The patient recovered well, and no recurrence was noted after 1 year of follow-up. Intravenous leiomyomatosis is rare. Imaging is helpful, but the final diagnosis of intravenous leiomyomatosis is usually made following surgical excision and histopathology. Early surgical resection is a better treatment modality. Elsevier 2022-09-07 /pmc/articles/PMC9464787/ /pubmed/36105826 http://dx.doi.org/10.1016/j.radcr.2022.08.020 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Lan, Suwei Wang, Xingcha Li, Yang Zhai, Mingjing Intravenous leiomyomatosis: A case study and literature review() |
title | Intravenous leiomyomatosis: A case study and literature review() |
title_full | Intravenous leiomyomatosis: A case study and literature review() |
title_fullStr | Intravenous leiomyomatosis: A case study and literature review() |
title_full_unstemmed | Intravenous leiomyomatosis: A case study and literature review() |
title_short | Intravenous leiomyomatosis: A case study and literature review() |
title_sort | intravenous leiomyomatosis: a case study and literature review() |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464787/ https://www.ncbi.nlm.nih.gov/pubmed/36105826 http://dx.doi.org/10.1016/j.radcr.2022.08.020 |
work_keys_str_mv | AT lansuwei intravenousleiomyomatosisacasestudyandliteraturereview AT wangxingcha intravenousleiomyomatosisacasestudyandliteraturereview AT liyang intravenousleiomyomatosisacasestudyandliteraturereview AT zhaimingjing intravenousleiomyomatosisacasestudyandliteraturereview |