Evidence map›Paper›PMID 41058781›Full record

ArticleCureus2025

Genomic Sequencing Insights Into a Rare Case of High-Risk Diffuse Large B-cell Lymphoma (DLBCL) Associated With Rubinstein-Taybi Syndrome.

Sreeja Ponnam, Prathima Guntipalli, Supriya Koya

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

3 authors.

Sreeja PonnamMedicine, University of Missouri-Kansas City (UMKC) School of Medicine, Kansas City, USA.
Prathima GuntipalliPreventive Medicine, Larkin Community Hospital, Miami, USA.
Supriya KoyaHematology and Oncology, OU Health Stephenson Cancer Center, Oklahoma City, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a rare case of a Rubinstein-Taybi syndrome (RSTS) patient who developed diffuse large B-cell lymphoma (DLBCL). RSTS is a very rare, genetic, developmental disease. RSTS patients have been reported to have some predilection for certain cancers. The patient had both germline and somatic mutations in the

Indexed as

braf (v-raf murine sarcoma viral oncogene homolog b1)crebbp (cyclic-amp-regulated enhancer-binding protein)diffuse large b-cell lymphoma (dlbcl)double hit lymphomaimmunostainingmyc (avian myelocytomatosis viral oncogene homolog)r-epochrubinstein-taybi syndrome (rsts)

Identifiers

PMID41058781
PMCPMC12498179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.