Evidence map›Paper›PMID 42078112›Full record

ArticleTurkish journal of surgery2026

Neuroblastoma treatment in children: Single-center case series and review of the literature.

Asmir Jonuzi, Ilhana Tinjak, Benjamin Kulovac, Predrag Ilic, Zlatan Zvizdic

Abstract read
In one paragraph

Article in Turkish journal of surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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.

Asmir JonuziDepartment of Pediatric Surgery, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.ORCID 0000-0002-5637-9510
Ilhana TinjakUniversity in Sarajevo Faculty of Medicine, Sarajevo, Bosnia and Herzegovina.ORCID 0009-0004-9070-5588
Benjamin KulovacDepartment of Urology, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.ORCID 0000-0002-0748-5971
Predrag IlicDepartment of Pediatric Urology, Institute for Mother and Child Health Care of Republic Serbia, Belgrade, Serbia.ORCID 0000-0002-2066-6796
Zlatan ZvizdicDepartment of Pediatric Surgery, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.ORCID 0000-0003-1238-880X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Description of the clinical presentation and tumor behavior, its general and pathological characteristics, diagnostic and therapeutic approaches, as well as treatment outcomes in children with neuroblastoma (NB) at a single-center. Special focus was placed on the duration of the diagnostic process and the correlation between disease stage, presence of metastases, and treatment outcomes. Given the small cohort, this report is presented as a descriptive case series complemented by a focused review of the literature NB. Material and Methods: A retrospective study was conducted for the time period from January 1 Results: The median age at diagnosis was 44 months. The largest number of patients were in the age group of 2-4 years, and most presented with stage four disease (according to International Neuroblastoma Staging System classification). The tumor was located in the adrenal gland in 92.3% of cases. The median survival time was 36 months. Patients had elevated serum neuron-specific enolase, urinary vanillylmandelic acid, as well as blood ferritin and lactate dehydrogenase levels. The most common symptoms were loss of appetite, presence of a palpable mass, and abdominal pain. Metastases were present in 76.9% of patients, and stage four was associated with aggressive metastatic dissemination. A multimodal approach was used in treatment. The median time from symptom onset to primary care physician consultation was 12 days, and the median time from physician consultation to diagnosis was 14 days. Relapse occurred in 46.2% of cases, most frequently in patients with stage four disease. A total of 7 patients (46.2%) survived. Conclusion: Advanced-stage disease at diagnosis, metastatic burden, and unfavorable outcomes, are dominating factors in our single-center experience. When compared with larger published cohorts, our findings align with global patterns. Due to inherent sample size limitations, these observations are hypothesis-generating and the need for larger, multicenter studies remains.

Indexed as

childcombined modality therapyneoplasm metastasisneoplasm stagingNeuroblastoma

Identifiers

PMID42078112
PMCPMC13237509

What Socratic 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 Socratic graph.