2016
DOI: 10.1002/cncy.21802
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Young Investigator Challenge: Molecular testing in noninvasive follicular thyroid neoplasm with papillary‐like nuclear features

Abstract: The current results indicate that NIFTP is a rare tumor if defined by strict criteria, that both the GEC and UPMC methods indicate abnormalities in NIFTP, and further independent study will be needed to better characterize the molecular and clinical characteristics of NIFTP. Cancer Cytopathol 2016;124:893-900. © 2016 American Cancer Society.

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Cited by 69 publications
(86 citation statements)
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“…Although lymph node metastasis in NIFTP is reported to be rare, we identified two such NIFTP cases. In both cases, the metastasis was to a single central lymph node, and the size of the metastatic focus was <2 mm.…”
Section: Methodsmentioning
confidence: 99%
“…Although lymph node metastasis in NIFTP is reported to be rare, we identified two such NIFTP cases. In both cases, the metastasis was to a single central lymph node, and the size of the metastatic focus was <2 mm.…”
Section: Methodsmentioning
confidence: 99%
“…These studies will also allow a reevaluation of the reproducibility and robustness of the diagnostic criteria for NIFTP. This need is highlighted by 2 recent studies reporting single cases diagnosed as NIFTP with regional lymph node metastasis 21, 23. The NIFTP diagnostic errors may occur in both follicular and papillary lineage directions.…”
Section: Introductionmentioning
confidence: 99%
“…Current data indicate the presence of mainly RAS mutations, along with PPARγ and THADA fusions [68]. However, some papers reported NIFTPs with the BRAF V600E mutation [69] or a coexistence of TERT promoter and RAS mutations [70]. Simultaneously, another paper emphasised the importance of tightening the classification criteria, since the BRAF V600E mutation has not been present in NIFTP cases, in which papillary structures were absent [69].…”
Section: Phenotypic and Molecular Heterogeneity Of Tc Subtypesmentioning
confidence: 99%