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Papillary thyroid carcinoma tall cell subtype (PTC-TC) and high-grade differentiated thyroid carcinoma tall cell phenotype (HGDTC-TC) have different clinical behaviour: a retrospective study of 1456 patients.
Ghossein, Ronald; Katabi, Nora; Dogan, Snjezana; Shaha, Ashok R; Tuttle, R Michael; Fagin, James A; Ganly, Ian; Xu, Bin.
Afiliação
  • Ghossein R; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Katabi N; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Dogan S; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Shaha AR; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Tuttle RM; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Fagin JA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Ganly I; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Xu B; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Histopathology ; 84(7): 1130-1138, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38528726
ABSTRACT

AIMS:

Papillary thyroid carcinoma, tall cell subtype (PTC-TC) is a potentially aggressive histotype. The latest World Health Organisation (WHO) classification introduced a novel class of tumours; namely, high-grade differentiated thyroid carcinoma (HGDTC), characterised by elevated mitotic count and/or necrosis, which can exhibit a tall cell phenotype (HGDTC-TC). METHODS AND

RESULTS:

We analysed the clinical outcomes in a large retrospective cohort of 1456 consecutive thyroid carcinomas with a tall cell phenotype, including PTC-TC and HGDTC-TC. HGDTC-TC is uncommon, accounting for 5.3% (77 of 1379) of carcinomas with tall cell morphology. HGDTC-TC was associated with significantly older age, larger tumour size, angioinvasion, gross extrathyroidal extension, higher AJCC pT stage, positive resection margin and nodal metastasis (P < 0.05). Compared with PTC-TC, HGDTC was associated with a significantly decreased DSS, LRDFS and distant metastasis-free survival (DMFS; P < 0.001). The 10-year DSS was 72 and 99%, the 10-year LRDFS was 61 and 92% and the 10-year DMFS was 53 and 97%, respectively, for HGDTC-TC and PTC-TC. On multivariate analysis, the classification (HGDTC-TC versus PTC-TC) was an independent adverse prognostic factor for DSS, LRDF, and DMFS when adjusted for sex, age, angioinvasion, margin status, AJCC pT and pN stage.

CONCLUSIONS:

Compared with PTC-TC, HGDTC-TC is associated with adverse clinicopathological features, a higher frequency of TERT promoter mutations (59% in HGDTC-TC versus 34% in PTC-TC) and incurs a significantly worse prognosis. HGDTC-TC is an independent prognostic factor for carcinoma with tall cell morphology. This validates the concept of HGDTC and the importance of tumour necrosis and high mitotic count for accurate diagnosis and prognosis of differentiated thyroid carcinomas.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Neoplasias da Glândula Tireoide / Câncer Papilífero da Tireoide Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Neoplasias da Glândula Tireoide / Câncer Papilífero da Tireoide Idioma: En Ano de publicação: 2024 Tipo de documento: Article