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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...

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Detalles Bibliográficos
Autores principales: Lan, Suwei, Wang, Xingcha, Li, Yang, Zhai, Mingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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
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AT zhaimingjing intravenousleiomyomatosisacasestudyandliteraturereview