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Risk of malignancy according to sub-classification of the atypia of undetermined significance or follicular lesion of undetermined significance (AUS/FLUS) category in the Bethesda system for reporting thyroid cytopathology.
Kim, S J; Roh, J; Baek, J H; Hong, S J; Shong, Y K; Kim, W B; Song, D E.
Affiliation
  • Kim SJ; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Roh J; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Baek JH; Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Hong SJ; Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Shong YK; Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim WB; Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Song DE; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Cytopathology ; 28(1): 65-73, 2017 Feb.
Article in En | MEDLINE | ID: mdl-27245883
OBJECTIVE: According to the Bethesda System for Reporting Thyroid Cytopathology, atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS) is a heterogeneous category that includes cases with architectural and/or nuclear atypia insufficient to warrant classification as malignant neoplasms. The ambiguous and descriptive characteristics of the AUS/FLUS category mean that the impact of the present guidelines on repeat fine needle aspiration (FNA) is unclear. The present study reclassified AUS/FLUS cases into four sub-categories and then correlated them with histological or cytological follow-up data to clarify the risk of malignancy. METHODS: Ninety-four cases of AUS/FLUS with available follow-up data were reviewed and assigned to one of four sub-categories: (i) AUS-N (nuclear atypia); (ii) AUS-A (architectural atypia); (iii) AUS-O (predominant oncocytic changes); and (iv) AUS-N/A (both nuclear and architectural atypia). The four sub-categories were correlated with subsequent histological or cytological follow-up data, including core needle biopsy, resection, or repeat FNA. RESULTS: Malignancy was identified in 34 of 94 cases (36.2%). The upper limit estimate for malignancy was 43.6%, and the lower limit estimate was speculated as 9.8%. The malignancy rate was highest in cases within the AUS-N sub-category (65.8%, range 16.6%-78.1%). CONCLUSIONS: The present study suggests that cases in the AUS/FLUS category have a higher risk of malignancy than previously thought. Because of the heterogeneous nature of the AUS/FLUS category, further sub-classification might be more effective in achieving appropriate risk stratification and better clinical management.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Gland / Thyroid Neoplasms / Thyroid Nodule / Cytodiagnosis Type of study: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Cytopathology Journal subject: PATOLOGIA Year: 2017 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Gland / Thyroid Neoplasms / Thyroid Nodule / Cytodiagnosis Type of study: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Cytopathology Journal subject: PATOLOGIA Year: 2017 Document type: Article Country of publication: United kingdom