Evidence map›Paper›PMID 33174155›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Incidence of Horner syndrome associated with neuroblastic disease.

Katarzyna Kuchalska, Monika Barełkowska, Katarzyna Derwich, Katarzyna Jończyk-Potoczna, Anna Gotz-Więckowska

Open access · hybridAbstract read
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. 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
0.1field-weighted citation impact, top 51% of its field
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, 5 citations in OpenAlex.

  1. Review
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 at 1 institution in 1 country.

Katarzyna KuchalskaKarol Marcinkowski University of Medical Sciences, Poznań, Poland. katarzyna.kathy0@gmail.com.ORCID 0000-0003-3859-1005
Monika BarełkowskaDepartment of Oncology, Hematology and Transplantology, Karol Marcinkowski University of Medical Sciences, Poznań, Poland.
Katarzyna DerwichDepartment of Oncology, Hematology and Transplantology, Karol Marcinkowski University of Medical Sciences, Poznań, Poland.ORCID 0000-0001-7239-4035
Katarzyna Jończyk-PotocznaDepartment of Paediatric Radiology, Poznań University of Medical Sciences, Poznań, Poland.
Anna Gotz-WięckowskaDepartment of Ophthalmology, Karol Marcinkowski University of Medical Sciences, Poznań, Poland.ORCID 0000-0003-3790-4583
Poznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHorner syndrome (HS) manifests in unilateral ptosis, miosis, enophthalmos, and anhedonia. It is most commonly caused by trauma or surgical procedures, but can also occur in pediatric patients as a result of tumors, especially neuroblastoma (NBL). The objective of this study was to analyze the incidence of HS in patients diagnosed with NBL.

methodsA retrospective analysis of data collected at the Department of Pediatric Oncology, Hematology, and Transplantology from 2004 to 2019 was performed. The study group included 119 patients younger than 18 years old, with 62 girls and 57 boys. All of them were diagnosed with a neuroblastic tumor.

resultsAmong the 119 patients, eight children (6.72%) were diagnosed with HS associated with NBL. Three of these patients presented to the clinic with HS, whereas HS developed after the surgical procedure to remove the tumor in four patients. The adrenal gland was the most frequent localization of the tumor. However, HS occurred more frequently in patients with mediastinum tumors. As a presenting symptom, HS occurred in 2 of 11 cases (18.18%) with mediastinum localization. All of the patients with HS were younger than 2 years old.

conclusionInvestigation of the cause of isolated HS is crucial because it can be the first symptom of NBL. However, the surgical procedure itself increases the risk of HS as a complication of NBL treatment.

Indexed as

BlepharoptosisHorner SyndromeNeuroblastomaAdolescentChildChild, PreschoolFemaleHumansIncidenceMaleRetrospective StudiesGanglioneuroblastomaMiosisNeuroblastomaPtosis

Identifiers

PMID33174155
PMCPMC8009793
OpenAlexW3098071849

What OpenQuestion holds

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LicenceCC BY
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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.