Low-risk palpablebreast masses removed using a vacuum-assisted hand-held device

被引:158
作者
Fine, RE
Whitworth, PW
Kim, JA
Harness, JK
Boyd, BA
Burak, WE
机构
[1] Ohio State Univ, Columbus, OH 43210 USA
[2] Breast Ctr, Marietta, GA USA
[3] Nashville Breast Ctr, Nashville, TN USA
[4] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[5] Univ Calif San Francisco E Bay, Oakland, CA USA
关键词
benign breast lesion; fibroadenoma; breast biopsy; mammotome;
D O I
10.1016/S0002-9610(03)00263-0
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: This study evaluates the safety, efficacy, and patient acceptance of a vacuum-assisted, hand-held biopsy device (Mammatome) in the percutaneous removal of breast masses using ultrasound guidance. Methods: A multicenter, nonrandomized study evaluated 216 women with low-risk palpable lesions. Lesions 1.5 to 3.0 cm in size were removed using an 8-gauge probe. Those lesions <1.5 cm were removed with the 11-gauge probe. Follow-up evaluation was performed at 10 days and 6 months after biopsy. Results: A total of 127 patients had biopsies using the 8-gauge probe, and 89 patients had biopsies using the 11-gauge probe. At 6-month follow-up, 98% of the lesions remained nonpalpable, 73% with no ultrasonographically visible evidence of the original lesion. Most complications were mild and anticipated. Most patients (98%) were satisfied with incision appearance, and 92% of patients would recommend the procedure to others. Conclusions: Percutaneous removal of palpable benign breast masses using the Mammotome system is feasible and safe, and yields high patient satisfaction. The results at 6 months after biopsy demonstrated the effectiveness of benign lesion removal, with correlative clinical data demonstrating lack of palpability and no need for additional procedures. Continuing evaluation of long-term efficacy is ongoing. C (C) 2003 Excerpta Medica, Inc. All rights reserved.
引用
收藏
页码:362 / 367
页数:6
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