2013
DOI: 10.1111/cyt.12093
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Hürthle cell presence alters the distribution and outcome of categories in the Bethesda system for reporting thyroid cytopathology

Abstract: We found that the rates of AUS/FLUS and FN/SFN categories in the Bethesda system were higher when Hürthle cells were present. After surgery, neoplastic and malignant outcomes were significantly higher in the Hürthle cell group.

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Cited by 22 publications
(45 citation statements)
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References 9 publications
(10 reference statements)
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“…This difference obviously resulted in an increased risk of malignancy for their HCN cases. Sometimes, it can be difficult to distinguish HCN from PTC with squamoid or Hürthle cell-like cytoplasm [6]. It was not surprising that high PTC percentages among malignant cases in the HCN category were also reported in other studies [4,6,7] although PMCs were excluded.…”
Section: Discussionmentioning
confidence: 99%
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“…This difference obviously resulted in an increased risk of malignancy for their HCN cases. Sometimes, it can be difficult to distinguish HCN from PTC with squamoid or Hürthle cell-like cytoplasm [6]. It was not surprising that high PTC percentages among malignant cases in the HCN category were also reported in other studies [4,6,7] although PMCs were excluded.…”
Section: Discussionmentioning
confidence: 99%
“…Another study demonstrated an even higher follow-up malignancy rate for cases diagnosed as FN/SFN with Hürthle cell (6/11, 54.5%) compared to those without Hürthle cell change (7/32, 18.8%) by excluding PMC [6]. However, our results revealed FNA cases diagnosed as AUS-H and HCN carried a malignancy risk of 7 and 24%, respectively, which is within the range of malignancy suggested by the BSRTC for the AUS and FN diagnostic categories.…”
Section: Discussionmentioning
confidence: 99%
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“…On the contrary, follicular carcinoma was the final histological diagnosis in only 21.1% of AUS/FLUS cases with architectural atypia [45]. The presence of oncocytes increases both the cytological diagnosis of AUS/FLUS and FNs as well as a final histological diagnosis of malignancy [46]. On the other hand, Wu et al [19] reported AUS/FLUS cases with a lower risk of malignancy (0 vs. 7%), but with a significantly higher risk of neoplasm (89 vs. 33%).…”
Section: Aus/flus Subclassification or Diminishment?mentioning
confidence: 99%
“…Some authors indicate that the frequency of cancer is higher in oxyphilic type of FLUS [47]. Others do not support such observations [13][14].…”
Section: Prace Oryginalnementioning
confidence: 94%