Mammotome core biopsy for mammary microcalcification - Analysis of 160 biopsies from 142 women with surgical and radiologic followup

Citation
J. Cangiarella et al., Mammotome core biopsy for mammary microcalcification - Analysis of 160 biopsies from 142 women with surgical and radiologic followup, CANCER, 91(1), 2001, pp. 173-177
Citations number
26
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER
ISSN journal
0008543X → ACNP
Volume
91
Issue
1
Year of publication
2001
Pages
173 - 177
Database
ISI
SICI code
0008-543X(20010101)91:1<173:MCBFMM>2.0.ZU;2-9
Abstract
BACKGROUND, Although stereotaxic fine-needle aspiration biopsy or core biop sy (14-gauge) have proven to be accurate techniques for the evaluation of m ammographically detected microcalcification, the development of the Mammoto me Biopsy System (Biopsys Medical, Inc., Irvine, Ca) has led many medical c enters to use this vacuum-assisted device for the sampling of microcalcific ation. METHODS. One hundred forty-two women underwent 160 stereotaxic Mammotome co re biopsies of mammographic calcification over a 1-year period. The stereot axic procedure was performed by radiologists using the Mammotome Biopsy Sys tem. Microcalcification was evident on specimen radiographs and microscopic slides in 99% of the cases. Excisional biopsy was recommended for diagnose s of atypia or carcinoma. Patients with benign diagnoses underwent mammogra phic followup. RESULTS, One hundred thirty-two benign, 12 atypical, and 15 adenocarcinoma diagnoses (comprising 1 lobular adenocarcinoma in situ [LCIS], 1 invasive d uctal adenocarcinoma [IDC], and 13 intraductal adenocarcinomas [DCIS]: 10 c omedo, 1 cribriform, 2 mixed cribriform and micropapillary) were rendered. Surgical excision in eight patients with atypia on Mammotome biopsy (two re fused surgery, two were lost to followup) showed ductal hyperplasia in thre e, atypical ductal hyperplasia (ADH) in three and DCIS (low grade, solid) i n two patients. Surgical excisions in 14 patients diagnosed with carcinoma (1 patient lost to followup) showed ADH in 3, ADH and LCIS in 1, residual D CIS in 8, IDC in 1, and microinvasive carcinoma in 1 patient. CONCLUSIONS. A diagnosis of atypia on Mammotome biopsy warranted excision o f the atypical area, yet the underestimation rate for the presence of carci noma remained low. The likelihood of an invasive component at excision was low for microcalcification diagnosed as DCIS on Mammotome biopsy. Mammotome biopsy proved to be an accurate technique for the sampling and diagnosis o f mammary microcalcification. (C) 2001 American Cancer Society.