Development of diagnosis support system using Real-time virtual sonography for breast imaging
| Project/Area Number |
25461999
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
General surgery
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| Research Institution | Aichi Medical University |
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Principal Investigator |
NAKANO Shogo 愛知医科大学, 医学部, 教授 (20351108)
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| Co-Investigator(Kenkyū-buntansha) |
FUJII Kimihito 愛知医科大学, 乳腺・内分泌外科, 准教授 (00524331)
KOUSAKA Junko 愛知医科大学, 乳腺・内分泌外科, 助教 (50440748)
ANDO Takahito 愛知医科大学, 乳腺・内分泌外科, 助教 (40634134)
吉田 美和 昭和大学, 医学部, 講師 (30556098)
手塚 理恵 愛知医科大学, 医学部, 助教 (20634132)
福富 隆志 愛知医科大学, その他部局等, 名誉教授 (30165302)
石口 恒男 愛知医科大学, 医学部, 教授 (70115525)
塩見 有佳子 (毛利有佳子 / 毛利 有佳子 / 塩見 有佳子(毛利有佳子)) 愛知医科大学, 医学部, 助教 (90465576)
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| Project Period (FY) |
2013-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥130,000 (Direct Cost: ¥100,000、Indirect Cost: ¥30,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
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| Keywords | 超音波fusion技術 / RVS / 超音波 / 乳腺良性腫瘍 / 磁気ナビゲーション / 乳癌 / 超音波fusion 技術 / MRI-detected lesion / MRIガイド下生検 / USガイド下生検 / breast ultrasound / リアルタイムバーチャルソノグラフィ / image fusion technique / BI-RADS3 / Surgeillance ultrasound / Neoadjuvant chemotherapy / Ｂｒｅａｓｔ uｌｔｒａｓｏｕｎｄ / Ｉｍａｇｅ ｆｕｓｉｏｎ ｔｅｃｈｎｉｑｕｅ / ＢＩ－ＲＡＤＳ ３ / Ｓｕｒｖｅｉｌｌａｎｃｅ ｕｌｔｒａｓｏｕｎｄ |
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| Outline of Final Research Achievements |
The aim of our study was verify the utility of surveillance US using real-time virtual sonography (RVS) in short-interval follow-up for BI-RADS US category 3 mass lesions. A total of 23 lesions classified as BI-RADS category 3 were enrolled. The US volume data was stored into RVS. Surveillance US was scheduled at 6, 12, and 24 months. All (100%) target lesions were detected. While performing the US, the examiner could make continuous comparison to the previous scan on the same cross section in the direction including the maximum diameter. The mean diameter of target lesion in baseline, 6, 12, and 24 months was 8.2mm , 8.4 mm , 8.1 mm , and 8.3 mm, respectively. There was no significant difference within the groups (p=0.785). RVS can be reproduced in their entirety for review at a later date by using stored US volume data Our results suggest that RVS is a reproducible technique in comparison of US images between different time phases for BI-RADS category 3 mass lesions.
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Report
(4 results)
Research Products
(10 results)
