Evidence map›Paper›PMID 27581232›Full record

ArticleBMJ case reports2016

Eosinophilia and multiple lymphadenopathy: Kimura disease, a rare, but benign condition.

Rafael García Carretero, Marta Romero Brugera, Noelia Rebollo-Aparicio, Oscar Vazquez-Gomez

Abstract readCase Reports
In one paragraph

Article in BMJ case reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Rafael García CarreteroDepartment of Internal Medicine, Hospital Universitario de Mostoles, Mostoles, Madrid, Spain.ORCID http://orcid.org/0000-0001-7532-4585
Marta Romero BrugeraDepartment of Emergency Medicine, Hospital Universitario de Mostoles, Mostoles, Madrid, Spain.
Noelia Rebollo-AparicioDepartment of Internal Medicine, Hospital Universitario de Mostoles, Mostoles, Madrid, Spain.
Oscar Vazquez-GomezDepartment of Infectious Diseases, Hospital Universitario de Mostoles, Mostoles, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kimura disease is a benign rare chronic inflammatory disorder of unknown aetiology. This disease is mainly endemic in Asia, although cases have also been reported in Europe and America. We describe a case in a 34-year-old Chinese man presenting with severe eosinophilia and multiple lymphadenopathy. Since our initial aim was to rule out the diagnosis of lymphoma, and given the limitations of our laboratory, we decided to perform an excision of one of the cervical lymph nodes. The histological diagnosis was consistent with Kimura disease. We review the epidemiology, the aetiology and clinical features of this entity.

Indexed as

AdultAngiolymphoid Hyperplasia with EosinophiliaAnti-Inflammatory AgentsDiagnosis, DifferentialHumansLymph NodesMalePrednisoneRare DiseasesTomography, X-Ray ComputedAnti-Inflammatory AgentsPrednisone

Identifiers

PMID27581232
PMCPMC5015188

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.