Evidence map›Paper›PMID 41993159›Full record

ArticleFrontiers in immunology2026

Behçet's syndrome-like features revealing myelodysplastic syndrome with

Andrej Pesic, Jelena Ljubicic, Milena Todorovic Balint, Kristel Klaassen, Marina Andjelkovic, Sonja Pavlovic, Maja Stojanovic

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in immunology, 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

7 authors.

Andrej Pesic *Clinic of Hematology, University Clinical Center of Serbia, Belgrade, Serbia.
Jelena Ljubicic *Clinic of Allergy and Immunology, University Clinical Center of Serbia, Belgrade, Serbia.
Milena Todorovic BalintClinic of Hematology, University Clinical Center of Serbia, Belgrade, Serbia.
Kristel KlaassenInstitute of Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Marina AndjelkovicInstitute of Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Sonja PavlovicInstitute of Molecular Genetics and Genetical Engineering, University of Belgrade, Belgrade, Serbia.
Maja StojanovicClinic of Allergy and Immunology, University Clinical Center of Serbia, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coexistence of Behçet's syndrome (BS) and myelodysplastic neoplasm (MDS) is increasingly recognized and is often referred to as MDS with BS-like features. These patients demonstrate a distinctive profile characterized by a high prevalence of trisomy 8 and limited response to conventional immunosuppressive therapy. However, the mutational profile of this rare entity remains almost entirely unexplored. Here, we report a 36-year-old female presenting with painful oral and genital ulcers who is subsequently diagnosed with an atypical form of BS. Nonetheless, whole-exome sequencing identified monoallelic

Indexed as

Behcet SyndromeMutationMyelodysplastic SyndromesTumor Suppressor Protein p53AdultExome SequencingFemaleHumansPhosphoproteinsRNA Splicing FactorsPhosphoproteinsRNA Splicing FactorsSF3B1 protein, humanTP53 protein, humanTumor Suppressor Protein p53Behçet’s syndromecase reportmyelodysplastic syndromeSF3B1TP53whole-exome sequencing

Identifiers

PMID41993159
PMCPMC13079325

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.