Purpose This study aims to analyze the imaging features of dilated ducts or ductal extension/relation of masses detected by ultrasound (US) and magnetic resonance imaging (MRI) and to correlate the results obtained through these 2 different imaging methods. Furthermore, the ability of the ductal relation pattern in differentiating benign and malignant lesions was explored. Methods and Materials Magnetic resonance imaging and US findings of 56 patients who had a pathologic diagnosis of papillary lesion were examined. Ductal findings were classified into four types for both imaging methods: intraductal form, extraductal form, mixed form, and no ductal relation. The correlation between MRI and US was then analyzed with respect to ductal findings. Statistical analyses were performed to determine the value of ductal patterns determined by these 2 imaging methods in the differentiation of benign and malignant papillary lesions. Results A total of 56 cases with papillomatosis (n = 11), papillomas (n = 29), and papillary breast carcinomas (n = 16) were included. There was a statistically significant correlation between all ductal patterns on US and the corresponding ductal signs on MRI. Palpable masses were statistically more common in patients with papillary breast carcinoma compared with other groups (P < 0.01). Segmental contrast enhancement occurred at a significantly higher rate in papillary breast carcinoma and papillomatosis patients, as compared with papilloma patients (P < 0.05). Conclusions Actual resolution of MRI is close to that of US in terms of the ability to demonstrate the ductal relation of masses. Segmental contrast enhancement on MRI and nonmass-like heterogeneous hypoechoic area or mass with multiple ductal extensions on US can be used in discriminating benign versus malignant papillary lesions. The absence of ductal sign in MRI indicates benignity.
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Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
Asia Univ, Dept Biotechnol, Taichung, Taiwan
China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, TaiwanMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Chen, Chih-Ping
Su, Yi-Ning
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Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, TaiwanMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Su, Yi-Ning
Chang, Tung-Yao
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Mackay Mem Hosp, Taiji Fetal Med Ctr, Taipei, TaiwanMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Chang, Tung-Yao
Li, Yu-Peng
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Mackay Mem Hosp, Dept Radiol, Taipei, TaiwanMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Li, Yu-Peng
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Tsai, Fuu-Jen
Hwang, Jonathan Kwei
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Loyola Marymount Univ, Los Angeles, CA 90045 USAMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
Hwang, Jonathan Kwei
Wang, Wayseen
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Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
Tatung Univ, Dept Bioengn, Taipei 104, TaiwanMackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
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Univ Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South KoreaUniv Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South Korea
Kim, Young Eun
Cha, Joo Hee
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Univ Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South KoreaUniv Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South Korea
Cha, Joo Hee
Kim, Hak Hee
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Univ Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South KoreaUniv Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South Korea
Kim, Hak Hee
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Shin, Hee Jung
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Chae, Eun Young
Choi, Woo Jung
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Univ Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South KoreaUniv Ulsan, Res Inst Radiol, Dept Radiol, Coll Med,Asan Med Ctr, Seoul, South Korea