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Molecular Breast Imaging Biopsy with a Dual-Detector System.
Hunt, Katie N; Conners, Amy Lynn; Gray, Lacey; Hruska, Carrie B; O'Connor, Michael K.
Affiliation
  • Hunt KN; From the Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
  • Conners AL; From the Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
  • Gray L; From the Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
  • Hruska CB; From the Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
  • O'Connor MK; From the Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
Radiol Imaging Cancer ; 6(4): e230186, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38847615
ABSTRACT
Purpose To develop a molecular breast imaging (MBI)-guided biopsy system using dual-detector MBI and to perform initial testing in participants. Materials and Methods The Stereo Navigator MBI Accessory biopsy system comprises a lower detector, upper fenestrated compression paddle, and upper detector. The upper detector retracts, allowing craniocaudal, oblique, or medial or lateral biopsy approaches. The compression paddle allows insertion of a needle guide and needle. Lesion depth is calculated by triangulation of lesion location on the upper detector at 0° and 15° and relative lesion activity on upper and lower detectors. In a prospective study (July 2022-June 2023), participants with Breast Imaging Reporting and Data System category 2, 3, 4, or 5 breast lesions underwent MBI-guided biopsy. After injection of 740 MBq technetium 99m sestamibi, craniocaudal and mediolateral oblique MBI (2-minute acquisition per view) confirmed lesion visualization. A region of interest over the lesion permitted depth calculation in the system software. Upper detector retraction allowed biopsy device placement. Specimen images were obtained on the retracted upper detector, confirming sampling of the target. Results Of 21 participants enrolled (mean age, 50.6 years ± 10.1 [SD]; 21 [100%] women), 17 underwent MBI-guided biopsy with concordant pathology. No lesion was observed at the time of biopsy in four participants. Average lesion size was 17 mm (range, 6-38 mm). Average procedure time, including preprocedure imaging, was 55 minutes ± 13 (range, 38-90 minutes). Pathology results included invasive ductal carcinoma (n = 1), fibroadenoma (n = 4), pseudoangiomatous stromal hyperplasia (n = 6), and fibrocystic changes (n = 6). Conclusion MBI-guided biopsy using a dual-head system with retractable upper detector head was feasible, well tolerated, and efficient. Keywords Breast Biopsy, Molecular Breast Imaging, Image-guided Biopsy, Molecular Breast Imaging-guided Biopsy, Breast Cancer Clinical trial registration no. NCT06058650 © RSNA, 2024.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Technetium Tc 99m Sestamibi / Molecular Imaging / Image-Guided Biopsy Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Radiol Imaging Cancer Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Technetium Tc 99m Sestamibi / Molecular Imaging / Image-Guided Biopsy Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Radiol Imaging Cancer Year: 2024 Document type: Article
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