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   <subfield code="a">10.1245/s10434-011-1635-1</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-011-1635-1</subfield>
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   <subfield code="a">Predictive Value of Cytologic Atypia in Indeterminate Thyroid Fine-Needle Aspirate Biopsies</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Meredith Kato, Daniel Buitrago, Tracy-Ann Moo, Xavier Keutgen, Raza Hoda, Joseph Ricci, Paul Christos, Grace Yang, Thomas Fahey III, Rasa Zarnegar]</subfield>
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   <subfield code="a">Background: Fine-needle aspiration (FNA) biopsies are the most accurate method for diagnosis of thyroid nodules. Unfortunately, biopsies are indeterminate 15-30% of the time and surgery is thus required for a definitive diagnosis. We aimed to determine whether specific descriptors of cytologic atypia mentioned in indeterminate FNA reports were associated with malignancy on final histopathology. Methods: Retrospective review of 1000 surgery patients identified 466 indeterminate FNA lesions that underwent either a hemi- or total thyroidectomy between 1998 and 2009. We screened FNA reports for specific descriptors of nuclear atypia. Univariate and multivariate analyses were performed to evaluate the independent effect of cytologic atypia descriptors on the risk of malignancy. Results: Nuclear atypia on FNA conferred a risk of malignancy of 42% (P&lt;0.0001). Risk of malignancy increased from 17% for zero descriptors to 81.2% when four or more descriptors of atypia were described. Nuclear grooves and inclusions together conferred a risk of malignancy, specificity, and false positive rate of 79.3%, 98.2% and 1.8% respectively. Conclusions: The presence of four or more descriptors of cytologic atypia or the presence of both nuclear inclusions and grooves together confers a high risk of malignancy on final histopathology and a low false positive rate. These findings should be taken into consideration when interpreting FNA reports and total thyroidectomy should be considered for those patients at higher risk.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="a">Kato</subfield>
   <subfield code="D">Meredith</subfield>
   <subfield code="u">Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="u">Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="a">Keutgen</subfield>
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   <subfield code="u">Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="u">Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="a">Christos</subfield>
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   <subfield code="u">Department of Public Health, Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="a">Yang</subfield>
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   <subfield code="u">Department of Pathology, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="a">Fahey III</subfield>
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   <subfield code="u">Department of Surgery, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY, USA</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/10(2011-10-01), 2893-2898</subfield>
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