Evidence map›Paper›PMID 40322419›Full record

ArticleCureus2025

Hemophagocytic Syndrome: A Serious Complication in Non-Hodgkin Lymphoma.

Samantha González Delgado, Rebeca Deyanira González García, Luis Paulo Ugarte Peláez, Diana Laura Morales Wong, Itzel Araceli Ortiz Meza

Abstract readCase Reports
PubMed Full text at PMC Publisher
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

5 authors.

Samantha González DelgadoInternal Medicine, Universidad Autónoma de Nuevo León, San Nicolás de los Garza, MEX.
Rebeca Deyanira González GarcíaInternal Medicine, Hospital Universitario de Monterrey, San Nicolás de los Garza, MEX.
Luis Paulo Ugarte PeláezHematology, Hospital Universitario de Monterrey, San Nicolás de los Garza, MEX.
Diana Laura Morales WongPathology, Hospital Universitario de Monterrey, San Nicolás de los Garza, MEX.
Itzel Araceli Ortiz MezaPathology, Hospital Universitario de Monterrey, San Nicolás de los Garza, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophagocytic syndrome (HPS) is a common complication in pediatric populations but a rare disease in adults. Also known as hemophagocytic lymphohistiocytosis (HLH), the few cases reported in adults have been primarily caused by severe infections and hematologic malignancies. We highlight the importance of considering HPS as a differential diagnosis in patients with persistent inflammatory conditions. This report describes the aggressive clinical course of a 58-year-old female patient. Prompt recognition of HPS may improve outcomes in such cases.

Indexed as

cerebral metastasishemophagocytic lymphohistiocytosis (hlh)large b cell lymphomamental status changesseverity of disease

Identifiers

PMID40322419
PMCPMC12050044

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.