Evidence map›Paper›PMID 36451640›Full record

ArticleCureus2022

Kikuchi-Fujimoto Disease: A Rare Cause of Pyrexia of Unknown Origin and Cervical Lymphadenopathy.

Abdalla Fadul, Eihab A Subahi, Elrazi A Ali, Habeeb Awadalkareem, Gihan Mohamed, Mohamed Elawad, Mohammad Sharaf Eldean, Adel Albozom

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2022. 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
0.2field-weighted citation impact, top 44% 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, 2 citations in OpenAlex.

  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

8 authors at 3 institutions in 2 countries.

Abdalla FadulInternal Medicine, Hamad Medical Corporation, Doha, QAT.
Eihab A SubahiInternal Medicine, Hamad Medical Corporation, Doha, QAT.
Elrazi A AliInternal Medicine, One Brooklyn Health/Interfaith Medical Center, Brooklyn, USA.
Habeeb AwadalkareemPediatrics, Hamad Medical Corporation, Doha, QAT.
Gihan MohamedInternal Medicine, Hamad Medical Corporation, Doha, QAT.
Mohamed ElawadRadiology, Hamad General Hospital, Doha, QAT.
Mohammad Sharaf EldeanHistopathology, Hamad Medical Corporation, Doha, QAT.
Adel AlbozomInternal Medicine, Hamad Medical Corporation, Doha, QAT.
Interfaith Medical Center · USHamad Medical Corporation · QAHamad General Hospital · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kikuchi-Fujimoto disease (KFD) is a benign disorder characterized by regional cervical lymphadenopathy with tenderness. Associated symptoms of KFD include low-grade fever, night sweats, weight loss, nausea, and sore throat. The disease is a sporadic disease known to have a worldwide distribution with a higher prevalence among Asian communities. Although the clinical and histopathological features point to a viral etiology, this hypothesis has not been proven yet. Generally, the diagnosis is made based on a lymph node excisional biopsy. Its recognition is crucial mainly because this disease can be mistaken for other disorders, including systemic lupus erythematosus or malignant lymphoma. Supportive treatment includes antipyretics, non-steroidal anti-inflammatory drugs, and corticosteroids. Spontaneous recovery occurs within a few weeks. Patients should be followed up for years to survey because there is a possibility of developing systemic lupus erythematosus. In this article, we report the case of a patient who presented with a fever of unknown origin and lymphadenopathy, treated with multiple antibiotic courses with no improvement. Workup including computed tomography of the neck with contrast and lymph node biopsy confirmed the diagnosis of KFD. His condition improved after administering analgesics and multivitamins, and he was advised to rest at home.

Indexed as

cervical lymphadenopathykikuchi-fujimoto diseasenecrotizing granulomatous lymphadenitispuo (pyrexia of unknown origin)unexplained fever

Identifiers

PMID36451640
PMCPMC9703205
OpenAlexW4307804379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.