Evidence map›Paper›PMID 31036733›Full record

ArticleBMJ case reports2019

Hypereosinophilia and severe bone disease in an African child: an unexpected diagnosis.

Sofia Bota, Pedro Alves, Claudia Constantino, Raquel Maia

Open access · bronzeAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in BMJ case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

4 authors at 1 institution in 1 country.

Sofia BotaWomen, Child and Adolescents Department, Hospital Dona Estefania, Lisboa, Portugal.ORCID http://orcid.org/0000-0003-4776-1053
Pedro AlvesRadiology Department, Hospital Dona Estefania, Lisboa, Portugal.
Claudia ConstantinoPediatric Oncology Department, Instituto Portugues de Oncologia de Lisboa Francisco Gentil EPE, Lisboa, Portugal.
Raquel MaiaWomen, Child and Adolescents Department, Hospital Dona Estefania, Lisboa, Portugal.
Hospital de Dona Estefânia · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypereosinophilic syndromes are rare in children. Sporadic, mild-severity FIP1L1-platelet-derived growth factor receptor α (PDGFRα) rearrangement cases have been reported, mainly in boys. We present the case of a 5-year-old girl referred from her African country of birth, due to severe constitutional symptoms, multifocal bone pain, headache, gastrointestinal complaints, cardiomyopathy and unexplained hypereosinophilia. She presented multiple end-organ diseases and striking bone involvement. Although she had a positive serology for

Indexed as

Adrenal Cortex HormonesAfricaAlbendazoleAnimalsAnthelminticsAntiparasitic AgentsBone DiseasesChild, PreschoolDrug CombinationsFemaleHumansHypereosinophilic SyndromeImatinib MesylateIvermectinmRNA Cleavage and Polyadenylation FactorsOncogene Proteins, FusionAdrenal Cortex HormonesAlbendazoleAnthelminticsAntiparasitic AgentsDrug CombinationsFIP1L1-PDGFRA fusion protein, humanImatinib MesylateIvermectinmRNA Cleavage and Polyadenylation FactorsOncogene Proteins, FusionProtein Kinase InhibitorsReceptor, Platelet-Derived Growth Factor alphapaediatric oncologyradiologytropical medicine (infectious disease)

Identifiers

PMID31036733
PMCPMC6506024
OpenAlexW2943350947

What OpenQuestion holds

Textmetadata
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.