Evidence map›Paper›PMID 40353679›Full record

ArticleTurkish archives of pediatrics2025

Evaluation of the Etiology of Granulomatous Lymphadenopathy in Children Admitted to a Tertiary Pediatric Infectious Clinic.

Fatma Tugba Cetin, Ümmühan Çay, Özlem Özgür Gündeslioğlu, Derya Alabaz, Nazlı Totik, Aysun Hatice Uğuz

Abstract read
In one paragraph

Article in Turkish archives of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Fatma Tugba CetinDepartment of Pediatric Infection, Çukurova University Faculty of Medicine, Adana, Türkiye.
Ümmühan ÇayDepartment of Pediatric Infection, Çukurova University Faculty of Medicine, Adana, Türkiye.
Özlem Özgür GündeslioğluDepartment of Pediatric Infection, Çukurova University Faculty of Medicine, Adana, Türkiye.
Derya AlabazDepartment of Pediatric Infection, Çukurova University Faculty of Medicine, Adana, Türkiye.
Nazlı TotikDepartment of Biostatistics, Çukurova University Faculty of Medicine, Adana, Türkiye.
Aysun Hatice UğuzDepartment of Medical Pathology, Çukurova University Faculty of Medicine, Adana, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Pediatric patients with histopathologically confirmed granulomatous lymphade- nopathy were evaluated etiologically. Materials and Methods: In this study, patients who presented to the tertiary pediatric infec- tious disease clinic with histopathologically confirmed granulomatous lymphadenopathy were retrospectively reviewed, and the etiological evaluation of granulomatous inflammation based on patient history, clinical findings, and additional tests were presented. Results: The study included 91 patients. In the study, 48 (52.7%) patients underwent biopsy from the cervical region, 21 (23.1%) patients underwent biopsy from the axillary region, 13 (14.3%) patients underwent biopsy from the submandibular and 9 (9.9%) patients underwent biopsy from lymph node sites other than these regions. Cervical lymphadenopathy was more common in patients over the age of 10, while axillary lymphadenopathy was more common in patients under the age of 5. A statistically significant difference was found between the age groups in the biopsy sites (P=.007). When the etiology of the patients was examined, it was found that 78 (85.7%) patients had infectious and 3 (3.3%) patients had non-infectious causes. The cause could not be determined for 10 (11%). There was a difference in etiology frequency according to the lymphadenopathy locations (P=.001). Conclusion: In this study, the most common etiology of granulomatous lymphadenopathy was shown to be infections, especially mycobacteria. Less common were toxoplasmosis, aspergil- lus, and cat scratches. Among non-infectious causes, chronic granulomatous disease should be kept in mind.

Identifiers

PMID40353679
PMCPMC12093400

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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.