Evidence map›Paper›PMID 33891138›Full record

ArticleWorld journal of surgery2021

Familial Non-Medullary Thyroid Carcinoma in Pediatric Age: Our Surgical Experience.

Claudio Spinelli, Irene Piccolotti, Alessia Bertocchini, Riccardo Morganti, Gabriele Materazzi, Massimo Tonacchera, Silvia Strambi

Open access · hybridAbstract read
In one paragraph

Article in World journal of surgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Observational
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  4. Observational
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Claudio SpinelliPediatric and Adolescent Surgery Division, Department of Pathology Surgery, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy. c.spinelli@dc.med.unipi.it.
Irene PiccolottiPediatric and Adolescent Surgery Division, Department of Pathology Surgery, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
Alessia BertocchiniPediatric and Adolescent Surgery Division, Department of Pathology Surgery, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
Riccardo MorgantiSection of Statistics, Department of Clinical and Experimental Medicine, University of Pisa, Via Paradisa 2, 56124, PisaPisa, Italy.
Gabriele MaterazziEndocrine Surgery Division, Department of Surgical Pathology, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
Massimo TonaccheraEndocrinology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
Silvia StrambiPediatric and Adolescent Surgery Division, Department of Pathology Surgery, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
University of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of the article was to evaluate the existence of significant clinical, pathological and prognostic differences between familial and sporadic form of pediatric non-medullary thyroid carcinoma, in order to tailor the therapeutic strategy to be adopted for patients with family history.

methodsWe analyzed the records of 76 pediatric patients that underwent surgery for differentiated thyroid cancer from 2014 to 2019 at the Surgical Pathology Department of the University of Pisa, Italy. Among these, 20 (26,3%) had positive family history (familial non-medullary thyroid carcinoma-FNMTC group) while 56 (73.7%) were affected by sporadic forms (sporadic non-medullary thyroid carcinoma-SNMTC group).

resultsIn our study, the correlation between the FNMTC and the SNMTC group showed no difference in terms of tumor features like multifocality, bilaterality, capsular/extracapsular invasion and the presence of vascular emboli. A statistical significance, on the other hand, was revealed by observation of clinical outcomes, such as distant metastasis (p = 0,022), persistence of disease (p = 0,054) and necessity of radioiodine sessions (p = 0,005).

conclusionsThese findings suggest that family history may have an independent role on the outcome, expressing its action through an intrinsic more aggressive biological behavior. Therefore, familial non-medullary thyroid carcinoma in children represents a nosological entity that requires an accurate pre-operative evaluation, an adequate surgical strategy and a careful follow up.

Indexed as

Iodine RadioisotopesThyroid NeoplasmsChildHumansRetrospective StudiesThyroid Cancer, PapillaryThyroidectomyIodine Radioisotopes

Identifiers

PMID33891138
PMCPMC8236051
OpenAlexW3154785503

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.