Evidence map›Paper›PMID 36582979›Full record

ArticleMediastinum (Hong Kong, China)2022

An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report.

Elisa Sicolo, Vittorio Aprile, Tommaso Ferrarello, Diana Bacchin, Maria Giovanna Mastromarino, Greta Alì, Marcello Carlo Ambrogi, Marco Lucchi, Stylianos Korasidis

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Mediastinum (Hong Kong, China), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 88% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 1 institution in 1 country.

Elisa SicoloThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Vittorio AprileThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Tommaso FerrarelloThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Diana BacchinThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Maria Giovanna MastromarinoThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Greta AlìUnit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.
Marcello Carlo AmbrogiThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Marco LucchiThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Stylianos KorasidisThoracis Surgery Division, Cardiac-Vascular and Thoracic Department, University Hospital of Pisa, Pisa, Italy.
Azienda Ospedaliera Universitaria Pisana · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mediastinal mass management may represent a real challenge for all the physicians who deal with it. Mediastinum, in fact, contains different vital structures which are often involved by growing neoplasms with increasing severity. Therefore, up to 60% of the patients with mediastinal mass are symptomatic, according to the structure involved. Different neoplasms may arise essentially from all mediastinal organs, whereas thymic epithelial tumors and lymphomas represent more than 90% of mediastinal tumors. Case Description: We report the first case described of a giant asymptomatic mediastinal mass in a 43-year-old male affected by Down syndrome (DS), turned out to be a thymoma, treated exclusively and successfully with radical surgery. Despite the absence of any symptoms, the giant thymoma infiltrated the diaphragm, the pericardium, the upper lobe of the left lung together with the left phrenic nerve resulting in the compression of heart and great vessels. Conclusions: To date, this is the first description of a thymic malignancy in a patient with DS, that usually is characterized by a low-incidence of solid tumor except for germ-cells ones. Surgery has been extremely challenging, due the clinical condition of the patient together with the tumor features; nevertheless, oncological radicality criteria were completely fulfilled. After four years from surgery, the patient is alive and still disease-free, highlighting the importance of radical surgery.

Indexed as

case reportDown syndrome (DS)Giant mediastinal massesmyasthenia gravis (MG)thymoma

Identifiers

PMID36582979
PMCPMC9792865
OpenAlexW4285186645

What Socratic holds

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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 Socratic graph.