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Long-term oncological outcomes of follicular thyroid cancer in adolescents and young adults: A nationwide population-based study.
van de Berg, Daniël J; Mooij, Christiaan F; van Trotsenburg, A S Paul; van Santen, Hanneke M; Terwisscha van Scheltinga, Sheila C E J; Vriens, Menno R; Kruijff, Schelto; Nieveen van Dijkum, Els J M; Engelsman, Anton F; Derikx, Joep P M.
Afiliação
  • van de Berg DJ; Department of Pediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Mooij CF; Department of Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • van Trotsenburg ASP; Department of Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • van Santen HM; Department of Pediatric Endocrinology, Wilhelmina Children's Hospital, Utrecht University Medical Center, University of Utrecht, Utrecht, The Netherlands.
  • Terwisscha van Scheltinga SCEJ; Department of Pediatric Oncology, Princess Máxima Center, Utrecht, The Netherlands.
  • Vriens MR; Department of Pediatric Surgical Oncology, Princess Máxima Center, Utrecht University Medical Center, University of Utrecht, Utrecht, The Netherlands.
  • Kruijff S; Department of Surgery, University Medical Center Utrecht, University of Utrecht, Utrecht, The Netherlands.
  • Nieveen van Dijkum EJM; Department of Surgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Engelsman AF; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Derikx JPM; Department of Surgery, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
World J Surg ; 2024 Jul 07.
Article em En | MEDLINE | ID: mdl-38972979
ABSTRACT

BACKGROUND:

Follicular thyroid carcinoma (FTC) in adolescents and young adults (AYAs) is rare and data on long-term oncological outcomes are scarce. This study aimed to describe the long-term recurrence and survival rates of AYAs with FTC, and identify risk factors for recurrence.

METHODS:

This is a retrospective cohort study combining two national databases, including all patients aged 15-39 years, diagnosed with FTC in The Netherlands between 2000 and 2016. Age, sex, tumor size, focality, positive margins, angioinvasion, pT-stage, and pN-stage were included in a Cox proportional hazard model to identify risk factors for recurrence.

RESULTS:

We included 192 patients. Median age was 31.0 years (IQR 24.7-36.3) and the male to female ratio was 14.1. Most patients presented with a minimally invasive FTC (MI-FTC) (95%). Five patients presented with synchronous metastases (2.6%), including two with locoregional metastases (1%) and three with distant metastases (1.6%). During a median follow-up of 12.0 years, three patients developed a recurrence (1.6%), of which one patient developed a local recurrence (33%), and two patients a distant recurrence (67%). Five patients died during follow-up (2.6%). Cause of death was not captured. A Cox proportional hazard model could not be performed due to the low number of recurrences.

CONCLUSIONS:

FTC in AYAs is generally characterized as a low-risk tumor, as it exhibits a very low recurrence rate, a high overall survival, and it typically presents as MI-FTC without synchronous metastases. These findings underscore the favorable long-term oncological prognosis of FTC in AYAs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article