Evidence map›Paper›PMID 32507920›Full record

ArticleVirchows Archiv : an international journal of pathology2020

Malignant teratoid tumor of the thyroid gland: an aggressive primitive multiphenotypic malignancy showing organotypical elements and frequent DICER1 alterations-is the term "thyroblastoma" more appropriate?

Abbas Agaimy, Leora Witkowski, Robert Stoehr, Joseph Christopher Castillo Cuenca, Carlos Alberto González-Muller, Alfred Brütting, Markus Bährle, Konstantinos Mantsopoulos, Randa M S Amin, Arndt Hartmann and 5 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Poorly differentiated thyroid carcinomas: conceptual controversy and clinical impact.Virchows Archiv : an international journal of pathology · 2024
    Pooled it
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  10. Spindle lesions in the thyroid: a cytological and histological review.Virchows Archiv : an international journal of pathology · 2025
    Review
  11. Teratocarcinosarcoma of the nasal cavity: challenges in the clinico-pathologic perspectives.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2025
    Review
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  20. Virchows Archiv (The European Journal of Pathology): Past and future.Virchows Archiv : an international journal of pathology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 4 countries.

Abbas AgaimyInstitute of Pathology, University Hospital Erlangen, Erlangen, Germany. abbas.agaimy@uk-erlangen.de.ORCID http://orcid.org/0000-0002-0445-8161
Leora WitkowskiDepartments of Human Genetics, McGill University, Montreal, Quebec, Canada.
Robert StoehrInstitute of Pathology, University Hospital Erlangen, Erlangen, Germany.
Joseph Christopher Castillo CuencaInstituto de Anatomía Patológica Arias Stella, Lima, Peru.
Carlos Alberto González-MullerInstituto de Anatomía Patológica Arias Stella, Lima, Peru.
Alfred BrüttingDepartment of Surgery, Malteser Waldkrankenhaus, Erlangen, Germany.
Markus BährleDepartment of Surgery, Malteser Waldkrankenhaus, Erlangen, Germany.
Konstantinos MantsopoulosDepartment of Otorhinolaryngology, Head and Neck Surgery, University of Erlangen-Nuremberg, Erlangen, Germany.
Randa M S AminDepartment of Pathology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Arndt HartmannInstitute of Pathology, University Hospital Erlangen, Erlangen, Germany.
Markus MetzlerDepartment of Pediatrics, University Hospital Erlangen, Erlangen, Germany.
Samir S AmrDepartment of Pathology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
William D FoulkesDepartments of Human Genetics, McGill University, Montreal, Quebec, Canada.
Manuel Sobrinho-SimõesInstituto de Investigação e Inovação em Saúde, Porto, Portugal.
Catarina EloyInstituto de Investigação e Inovação em Saúde, Porto, Portugal.
Universitätsklinikum Erlangen · DEKing Fahad Specialist Hospital · SAMalteser Waldkrankenhaus Erlangen · DEUniversidade do Porto · PTFriedrich-Alexander-Universität Erlangen-Nürnberg · DEMcGill University · CAMcGill University Health Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary thyroid teratomas are exceedingly rare. Mature and immature variants recapitulate their gonadal counterparts (predilection for infants/children, triphasic germ layer differentiation, and favorable outcome). On the other hand, the so-called malignant teratomas affect predominantly adults and elderly, are highly aggressive, and, according to a few published cases, harbor DICER1 mutations. We describe three highly aggressive sporadic malignant teratoid thyroid tumors in 2 females (17 and 45 years) and one male (17 years). Histology showed triphasic neoplasms composed of solid nests of small primitive monomorphic cells embedded in a cellular stroma with primitive immature rhabdomyosarcoma-like (2) or pleomorphic sarcoma-like (1) phenotype. The third component was represented by TTF1+/PAX8+ primitive teratoid epithelial tubules reminiscent of primitive thyroid follicles and/or Wilms tumor, admixed with scattered respiratory- or enteric-type tubules, neuroepithelial rosettes, and fetal-type squamoid nests. Foci of cartilage were seen in two cases, but none contained mature organoid adult-type tissue or skin adnexa. SALL4 was expressed in the small cell (2) and stromal (1) component. Other germ cell markers were negative. Molecular testing revealed a known "hotspot" pathogenic DICER1 mutation in two cases. In addition, case 1 had a missense TP53 variant. This type of thyroid malignancy is distinct from genuine teratomas. The immunoprofile suggests primitive thyroid- or branchial cleft-like differentiation. Given that "blastoma" is a well-accepted terminology in the spectrum of DICER1-associated malignancies, the term "thyroblastoma" might be more convenient for these malignant teratoid tumors of the thyroid gland. Relationship of thyroblastoma to the DICER1 syndrome remains to be addressed.

Indexed as

AdolescentAgedDEAD-box RNA HelicasesFemaleHumansMaleMiddle AgedMutationRibonuclease IIITeratomaTerminology as TopicThyroid NeoplasmsDEAD-box RNA HelicasesDICER1 protein, humanRibonuclease IIIDICER1Germ cell tumorHead and neckMalignant teratomaRhabdomyosarcomaTeratocarcinosarcomaThyroblastomaThyroid

Identifiers

PMID32507920
PMCPMC7683491
OpenAlexW3033663897

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.