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Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?

OBJECTIVE: To investigate whether the ultrasound microcystic pattern (MCP) can accurately predict borderline ovarian tumors (BOTs). METHODS: A retrospective collection of 393 patients who met the inclusion criteria was used as the study population. Indicators that could well identify BOT in differen...

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Autores principales: Liu, Danyi, Lyu, Guorong, Lai, Hongwei, Li, Liya, Gan, Yaduan, Yang, Shuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416400/
https://www.ncbi.nlm.nih.gov/pubmed/37563718
http://dx.doi.org/10.1186/s13048-023-01253-8
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author Liu, Danyi
Lyu, Guorong
Lai, Hongwei
Li, Liya
Gan, Yaduan
Yang, Shuping
author_facet Liu, Danyi
Lyu, Guorong
Lai, Hongwei
Li, Liya
Gan, Yaduan
Yang, Shuping
author_sort Liu, Danyi
collection PubMed
description OBJECTIVE: To investigate whether the ultrasound microcystic pattern (MCP) can accurately predict borderline ovarian tumors (BOTs). METHODS: A retrospective collection of 393 patients who met the inclusion criteria was used as the study population. Indicators that could well identify BOT in different pathological types of tumors were derived by multivariate unordered logistic regression analysis. Finally, the correlation between ultrasound MCP and pathological features was analyzed. RESULTS: (1) MCP was present in 55 of 393 ovarian tumors, including 34 BOTs (34/68, 50.0%), 16 malignant tumors (16/88, 18.2%), and 5 benign tumors (5/237, 2.1%). (2) Univariate screening showed significant differences (P < 0.05) in patient age, CA-125 level, ascites, > 10 cyst locules, a solid component, blood flow, and MCP among BOTs, benign ovarian tumors, and malignant ovarian tumors. (3) Multivariate unordered logistic regression analysis showed that the blood flow, > 10 cyst locules, and MCP were significant factors in identifying BOTs (P < 0.05). (4) The pathology of ovarian tumors with MCP showed "bubble"- or "fork"- like loose tissue structures. CONCLUSION: MCP can be observed in different pathological types of ovarian tumors and can be used as a novel sonographic marker to differentiate between BOTs, benign tumors and malignant tumors. MCP may arise as a result of anechoic cystic fluid filling the loose tissue gap.
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spelling pubmed-104164002023-08-12 Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors? Liu, Danyi Lyu, Guorong Lai, Hongwei Li, Liya Gan, Yaduan Yang, Shuping J Ovarian Res Research OBJECTIVE: To investigate whether the ultrasound microcystic pattern (MCP) can accurately predict borderline ovarian tumors (BOTs). METHODS: A retrospective collection of 393 patients who met the inclusion criteria was used as the study population. Indicators that could well identify BOT in different pathological types of tumors were derived by multivariate unordered logistic regression analysis. Finally, the correlation between ultrasound MCP and pathological features was analyzed. RESULTS: (1) MCP was present in 55 of 393 ovarian tumors, including 34 BOTs (34/68, 50.0%), 16 malignant tumors (16/88, 18.2%), and 5 benign tumors (5/237, 2.1%). (2) Univariate screening showed significant differences (P < 0.05) in patient age, CA-125 level, ascites, > 10 cyst locules, a solid component, blood flow, and MCP among BOTs, benign ovarian tumors, and malignant ovarian tumors. (3) Multivariate unordered logistic regression analysis showed that the blood flow, > 10 cyst locules, and MCP were significant factors in identifying BOTs (P < 0.05). (4) The pathology of ovarian tumors with MCP showed "bubble"- or "fork"- like loose tissue structures. CONCLUSION: MCP can be observed in different pathological types of ovarian tumors and can be used as a novel sonographic marker to differentiate between BOTs, benign tumors and malignant tumors. MCP may arise as a result of anechoic cystic fluid filling the loose tissue gap. BioMed Central 2023-08-11 /pmc/articles/PMC10416400/ /pubmed/37563718 http://dx.doi.org/10.1186/s13048-023-01253-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Danyi
Lyu, Guorong
Lai, Hongwei
Li, Liya
Gan, Yaduan
Yang, Shuping
Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title_full Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title_fullStr Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title_full_unstemmed Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title_short Can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
title_sort can the ultrasound microcystic pattern accurately predict borderline ovarian tumors?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416400/
https://www.ncbi.nlm.nih.gov/pubmed/37563718
http://dx.doi.org/10.1186/s13048-023-01253-8
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