Evidence map›Paper›PMID 35212317›Full record

ReviewPathologica2022

New insights in gastrointestinal "pediatric" neoplasms in adult patients: pancreatoblastoma, hepatoblastoma and embryonal sarcoma of the liver. A practical approach by GIPPI-GIPAD Groups.

Vassilena Tsvetkova, Gaetano Magro, Giuseppe Broggi, Claudio Luchini, Filippo Cappello, Chiara Caporalini, Anna Maria Buccoliero, Luisa Santoro

Open access · diamondAbstract readReview
In one paragraph

Review in Pathologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Blastomas of the digestive system in adults: A review.World journal of gastrointestinal surgery · 2024
    Review
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  7. Review
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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

8 authors at 3 institutions in 1 country.

Vassilena TsvetkovaDepartment of Diagnostics and Public Health, Section of Pathology, Verona University and Hospital Trust; Verona, Italy.
Gaetano MagroDepartment of Medical and Surgical Sciences and Advanced Technologies "G. F. Ingrassia", Anatomic Pathology, University of Catania, 95123 Catania, Italy.
Giuseppe BroggiDepartment of Medical and Surgical Sciences and Advanced Technologies "G. F. Ingrassia", Anatomic Pathology, University of Catania, 95123 Catania, Italy.
Claudio LuchiniDepartment of Diagnostics and Public Health, Section of Pathology, Verona University and Hospital Trust; Verona, Italy.
Filippo CappelloDepartment of Pathology, Azienda Ospedaliera Universitaria di Padova, Padova, Italy.
Chiara CaporaliniPathology Unit, Meyer Children Hospital, Florence, Italy.
Anna Maria BuccolieroPathology Unit, Meyer Children Hospital, Florence, Italy.
Luisa SantoroDepartment of Pathology, Azienda Ospedaliera Universitaria di Padova, Padova, Italy.
Azienda Ospedaliera di Padova · ITMeyer Children's Hospital · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric solid neoplasms are rare and very different from those observed in adults. The majority of them are referred to as embryonal because they arise as a result of alterations in the processes of organogenesis or normal growth and are characterized by proliferation of primitive cells, reproducing the corresponding tissue at various stages of embryonic development. This review will focus on embryonal gastrointestinal pediatric neoplasms in adult patients, including pancreatoblastoma, hepatoblastoma, and embryonal sarcoma of the liver. Although they are classically considered pediatric neoplasms, they may (rarely) occur in adult patients. Hepatoblastoma represents the most frequent liver neoplasm in the pediatric population, followed by hepatocellular carcinoma and embryonal sarcoma of the liver; while pancreatoblastoma is the most common malignant pancreatic tumor in childhood. Both in children and adults, the mainstay of treatment is complete surgical resection, either up front or following neoadjuvant chemotherapy. Unresectable and/or metastatic neoplasms may be amenable to complete delayed surgery after neoadjuvant chemotherapy. However, these neoplasms display a more aggressive behavior and overall poorer prognosis in adults than in children, probably because they are diagnosed in later stages of diseases.

Indexed as

HepatoblastomaLiver NeoplasmsPancreatic NeoplasmsSarcomaChildFemaleHumansPregnancygastro-intestinal tumorshepatic embryonal sarcomahepatoblastomapancreatoblastomapediatric tumors

Identifiers

PMID35212317
PMCPMC9040550
OpenAlexW4214715000

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.