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   <subfield code="a">10.1245/s10434-011-1959-x</subfield>
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   <subfield code="a">Sensitivity of Axillary Specimen X-ray to Predict Nodal Count and Positivity</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Chad Johnson, Soheila Korourian, Brian Badgwell, Robert Fincher, Carol Dell, C. Don Bice, Cristiano Boneti, Kent Westbrook, V. Klimberg]</subfield>
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   <subfield code="a">Background: The number of examined axillary lymph nodes (ALN) has been proposed as an indicator of prognosis along with quality and adequacy in breast cancer surgery. The purpose of this study was to examine the utility of imaging axillary specimens with x-ray (lymphogram) to determine the number of lymph nodes. We sought to determine the sensitivity and specificity of a lymphogram in identifying nodal positivity. Methods: Patients who underwent sentinel lymph node (SLN) and axillary lymph node dissections (ALND) were prospectively accrued to this double-blinded, single-institution trial from December 2009 to January 2011. A single physician interpreted all lymphograms for the number of ALNs and positivity determined by size, spiculations, irregularities, and calcifications. Results: Twenty female (age 50.8±14.3years) patients were accrued to the study. The lymphogram located more lymph nodes compared with pathology in 11 of 16 cases (68.8%). In these 11 cases, lymphogram identified 170 nodes and the pathologist located 132 (77.6%). Of the 16 ALND specimens, 6 were from patients naive to chemotherapy and averaged 13.8±6.6 nodes; 10 were from neoadjuvant chemotherapy patients and had an average number of 14.9±7.4 nodes. In neoadjuvant chemotherapy patients, sensitivity of the lymphogram to detect nodal positivity was 91.7% and specificity was 33.3%. Conclusions: This study demonstrated that lymphogram accurately identifies nodal count. This can be used for documentation of an adequate ALND for reimbursement. Furthermore, there may be potential value of lymphogram in intraoperative determination of nodal positivity.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="a">Johnson</subfield>
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   <subfield code="u">Division of Breast Surgical Oncology, Department of Surgery, University of Arkansas for Medical Sciences, Winthrop P. Rockefeller Cancer Institute, Little Rock, AR, USA</subfield>
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   <subfield code="a">Korourian</subfield>
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   <subfield code="u">Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA</subfield>
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   <subfield code="a">Badgwell</subfield>
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   <subfield code="u">Division of Surgical Oncology, Department of Surgery, University of Arkansas for Medical Sciences Winthrop P. Rockefeller Cancer Institute, Little Rock, AR, USA</subfield>
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   <subfield code="a">Don Bice</subfield>
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   <subfield code="u">Division of Breast Surgical Oncology, Department of Surgery, University of Arkansas for Medical Sciences, Winthrop P. Rockefeller Cancer Institute, Little Rock, AR, USA</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/11(2011-10-01), 3181-3186</subfield>
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