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Clinical behaviour of papillary thyroid cancer oncocytic variant: stage-matched comparison versus classical and tall cell variant papillary thyroid cancer.

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Revista espanola de medicina nuclear e imagen molecular 📖 저널 OA 2.6% 2023: 0/5 OA 2024: 0/5 OA 2025: 0/8 OA 2026: 1/19 OA 2023~2026 2023 Vol.42(2) p. 100-105
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출처

Okuyucu K, Ince S, Cinar A, San H, Samsum M, Dizdar N

📝 환자 설명용 한 줄

[OBJECTIVE] Papillary thyroid cancer (PTC) has many variants and most of them are mild tumors.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p=0.023
  • p-value p=0.03
  • 연구 설계 cohort study

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↓ .bib ↓ .ris
APA Okuyucu K, Ince S, et al. (2023). Clinical behaviour of papillary thyroid cancer oncocytic variant: stage-matched comparison versus classical and tall cell variant papillary thyroid cancer.. Revista espanola de medicina nuclear e imagen molecular, 42(2), 100-105. https://doi.org/10.1016/j.remnie.2022.09.007
MLA Okuyucu K, et al.. "Clinical behaviour of papillary thyroid cancer oncocytic variant: stage-matched comparison versus classical and tall cell variant papillary thyroid cancer.." Revista espanola de medicina nuclear e imagen molecular, vol. 42, no. 2, 2023, pp. 100-105.
PMID 36155103 ↗

Abstract

[OBJECTIVE] Papillary thyroid cancer (PTC) has many variants and most of them are mild tumors. Oncocytic variant (OV) is a rare subtype of PTC. There are controversial results about its prognosis in the literature. We investigated its aggressivity and clinical course by comparing it with classical variant (CV) and tall cell variant (TV) of PTC over a stage-matched design.

[MATERIAL AND METHODS] Pure 100 OV, 71TV and 1219 CV were included in this retrospective cohort study. OV was compared with CV and TV according to independent prognostic parameters. OV was also compared stage by stage with CV and TV for recurrence.

[RESULTS] Mean age was 46,8 years and male/female ratio 25/75 for OV. The recurrence rates in our study were 16% in OV, 13,5% in CV and 56% in TV. There is a statistically significant difference according to recurrence between stage I and stage IV OV and CV (p=0.023, p=0.03, respectively). There is also a statistically significant difference between stage I and stage IV OV and TV according to recurrence (p=0.001, p=0.024, respectively). OV can be supposed to behave between CV and TV, but very closer to CV.

[CONCLUSIONS] OV seems to be slightly more aggressive than CV. Despite an inadequate sample size for stage II and III, our findings imply an increased recurrence risk for OV than CV at the advanced stages (stage III and IV) and CV has an unfavorable prognosis than OV at early stages (stage I and II) according to stage-matched model.

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