Evidence map›Paper›PMID 42608735›Full record

SynthesisGenes, chromosomes & cancer2026

Hematologic Manifestations of Constitutional Trisomy 8 Mosaicism: Two Cases and a Systematic Review of Cytogenetically Confirmed Patients.

Andrea Magni, Riccardo Pagani, Antonio Maria Alviano, Lucia Pia Bruno, Rebecca Fumagalli, Grazia Fazio, Marta Galbiati, Federica Mottadelli, Andrea Biondi, Vincenzo L'Imperio and 3 more

Abstract readCase ReportsSystematic Review
In one paragraph

Synthesis in Genes, chromosomes & cancer, 2026. 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
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.

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

13 authors.

Andrea MagniSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0009-0008-7374-5579
Riccardo PaganiSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0000-0003-4109-5395
Antonio Maria AlvianoSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0009-0002-0686-6203
Lucia Pia BrunoSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0009-0008-0490-8637
Rebecca FumagalliSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0009-0001-8419-1566
Grazia FazioSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0000-0001-7077-8422
Marta GalbiatiS.C. Genetica Medica, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.
Federica MottadelliLaboratorio Ultraspecialistico di Patologia Clinica-Ematologia, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.
Andrea BiondiCentro Tettamanti, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.
Vincenzo L'ImperioSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0000-0002-9284-2998
Adriana Cristina BalduzziSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID https://orcid.org/0000-0002-5879-0610
Francesca VendeminiDepartment of Pediatrics, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.
Francesco SaettiniCentro Tettamanti, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.ORCID https://orcid.org/0000-0003-0767-3905

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Constitutional trisomy 8 mosaicism (CT8M) is a rare chromosomal disorder associated with congenital anomalies and hematologic malignancies, although its hematologic spectrum remains poorly defined. We report two institutional cases and performed a systematic review restricted to patients with trisomy 8 confirmed in both hematopoietic and non-hematopoietic tissues. Among 61 patients, hematologic abnormalities ranged from macrocytosis and cytopenias to dysplastic bone marrow changes and malignancies. No clear age-dependent peak of transformation emerged. Our findings suggest that CT8M represents a lifelong state of mosaic hematopoiesis with variable hematologic manifestations and uncertain malignant potential.

Indexed as

Hematologic NeoplasmsTrisomyUniparental DisomyAdultChromosomes, Human, Pair 8CytopeniaFemaleHumansMaleMosaicismbone marrow dysplasiaclonal evolutionconstitutional trisomy 8 mosaicismmyeloid neoplasmssomatic variants

Identifiers

PMID42608735
PMCPMC13481818

What OpenQuestion 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 OpenQuestion graph.