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Molecular Profile and Clinical-Pathologic Features of the Follicular Variant of Papillary Thyroid Carcinoma: An Unusually High Prevalence of ras Mutations

American Journal of Clinical Pathology · 2003 · Vol. 120(1) · pp. 71–77
Zhaowen ZhuManoj GandhiMarina N. NikiforovaAndrew H. FischerYuri E. Nikiforov

Abstract

The follicular variant (FV) of papillary thyroid carcinoma is characterized by a follicular growth pattern and cytologic features of papillary carcinoma. ret/PTC rearrangements are common in classic papillary thyroid carcinoma (PTC) and PAX8-PPAR gamma and ras mutations in follicular thyroid carcinoma. Their prevalence in FV has not been established. We studied these genetic alterations and clinical-pathologic features in 30 FV cases and compared those with 46 non-FV papillary carcinomas. FV cases revealed 1 ret/PTC rearrangement (3%) and 13 ras mutations (43%). Non-FV cases harbored 13 ret/PTC (28%) (P = .006) and no ras mutations (P = .0002). No PAX8-PPAR gamma was found in either group. FV cases demonstrated a significantly higher prevalence of tumor encapsulation, angiovascular invasion, and poorly differentiated areas and a lower rate of lymph node metastases. These data indicate that the FV of papillary carcinoma has a distinct set of molecular alterations and is characterized by a high frequency of ras point mutations.

Thyroid Cancer Diagnosis and TreatmentCancer-related gene regulationCancer-related Molecular PathwaysThyroid carcinomaPathologyPAX8CarcinomaFollicular phaseThyroidThyroid neoplasmPoint mutationPapillary carcinomaCancer research

MeSH terms

PAX8 Transcription FactorAdultCarcinoma, PapillaryDNA-Binding ProteinsDNA, NeoplasmFemaleHumansMaleNuclear ProteinsGenes, rasThyroid NeoplasmsTranscription FactorsGene RearrangementTrans-ActivatorsPoint Mutation
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