Evidence map›Paper›PMID 30723294›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2019

Angiosarcoma and anaplastic carcinoma of the thyroid are two distinct entities: a morphologic, immunohistochemical, and genetic study.

Elisabetta Kuhn, Moira Ragazzi, Alessia Ciarrocchi, Federica Torricelli, Dario de Biase, Eleonora Zanetti, Alessandra Bisagni, Stefania Corrado, Silvia Uccella, Stefano La Rosa and 3 more

Open access · bronzeAbstract read
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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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  19. IGF2BP1 is the first positive marker for anaplastic thyroid carcinoma diagnosis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
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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

13 authors at 6 institutions in 2 countries.

Elisabetta KuhnPathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Moira RagazziPathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Alessia CiarrocchiLaboratory of Translational Research, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Federica TorricelliLaboratory of Translational Research, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Dario de BiaseDepartment of Pharmacy and Biotechnology (Dipartimento di Farmacia e Biotecnologie) - Molecular Pathology Unit, Azienda USL di Bologna, University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0002-0609-8817
Eleonora ZanettiPathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Alessandra BisagniPathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.
Stefania CorradoDepartment of Anatomic Pathology, Azienda Ospedaliero-Universitaria, Modena, Italy.
Silvia UccellaDepartment of Medicine and Surgery, University of Insumbria, Varese, Italy.
Stefano La RosaService of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland.
Massimo BongiovanniService of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland.ORCID http://orcid.org/0000-0001-9846-6682
Simona LositoNational Cancer Institute G. Pascale, Naples, Italy.
Simonetta PianaPathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy. simonetta.piana@ausl.re.it.ORCID http://orcid.org/0000-0003-4875-6977
Ospedale Santa Maria · ITUniversity of Lausanne · CHAzienda Ospedaliero-Universitaria di Modena · ITAzienda USL di Bologna · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Insubria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiosarcoma and anaplastic carcinoma are the most lethal neoplasms of the thyroid worldwide and share some similarities, which have led to a longstanding controversy on their etiopathological relationship. Thyroid angiosarcomas are characterized by vessel formation and an immunophenotype common to endothelial cells, while anaplastic carcinomas are partially or wholly composed of mesenchymal-like cells that have lost the morphologic and functional features of normal thyroid follicular cells. To investigate whether angiosarcomas represent the endothelial extreme of the differentiation spectrum of carcinomas or they are bona fide vascular neoplasms, we studied the clinico-morphologic and genetic characteristics of a series of 10 angiosarcomas and 22 anaplastic carcinomas. Immunohistochemically, among the endothelial markers, CD31 and ERG were the most consistently expressed in angiosarcomas. Among the markers of thyroid origin, PAX8 was the most reliable in anaplastic carcinomas, while TTF-1 reactivity was found in only 5% of anaplastic carcinomas and thyroglobulin was always negative. Pankeratin reacted with most angiosarcomas and anaplastic carcinomas and is therefore not useful in the differential diagnosis. Interestingly a mutated pattern of p53 immunostaining prompted a diagnosis of anaplastic carcinoma. To compare the genetic profile, we used the NGS approach to sequence hotspot regions within a panel of 57 genes. As a result, only a few mutations were found in angiosarcomas and all of them were single events (no TP53 or TERT mutation). On the other hand, anaplastic carcinomas were characterized by a higher number of mutations, and TP53 and TERT promoter mutations were the most frequent genetic alterations. The lack in angiosarcomas of the common mutations identified in anaplastic carcinomas supports a different genetic origin and strongly suggests that, in spite of a shared sarcomatous morphology and a similar clinical aggressiveness, angiosarcomas and anaplastic carcinomas rely on a completely different set of genetic alterations during their evolution.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinomaFemaleHemangiosarcomaHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryMaleMiddle AgedThyroid NeoplasmsBiomarkers, Tumor

Identifiers

PMID30723294
OpenAlexW2912503167

What Socratic holds

Textmetadata
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 Socratic graph.