Evidence map›Paper›PMID 35444918›Full record

ArticleCureus2022

Kikuchi-Fujimoto Disease: A Rare Benign Cause of Lymphadenopathy That Mimics Malignant Lymphoma.

Israa Gism Elseed, Haitham Osman, Osman Ahmedfiqi, Fatima Najmi, Abdulqader Al-Hebshi

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

5 authors at 3 institutions in 1 country.

Israa Gism ElseedMedicine, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.
Haitham OsmanHematology, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.
Osman AhmedfiqiMedicine, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.
Fatima NajmiPathology, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.
Abdulqader Al-HebshiPediatric Hematology-Oncology, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.
National Guard Health Affairs · SAPrince Mohammed bin Abdulaziz Hospital · SAKing Saud bin Abdulaziz University for Health Sciences · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kikuchi-Fujimoto disease (KFD), also called histiocytic necrotizing lymphadenitis, is a benign self-limited disease involving lymph node enlargement with unclear causes and high fever. It was first seen in Japan and has wide array of differentials, and thus it can be confused with other causes of lymphadenitis leading to an incorrect treatment. We describe a case of a 34-year-old man with prolonged painless cervical lymphadenopathy and fever, in whom KFD, that is histiocytic necrotizing lymphadenitis, was diagnosed after the gold standard test of lymph node biopsy. Physical examination, history, and other relevant investigations were performed to rule out infectious and autoimmune causes. For management, prednisone 80mg and hydroxychloroquine were given, which lead to an uneventful full recovery. Our findings were compared to other similar studies conducted in the past. KFD is a self-limited condition that usually resolves by itself. KFD should be considered in the differential diagnosis of lymphadenopathy. An accurate diagnosis requires close collaboration between clinicians and pathologists. Early diagnosis of KFD allows reducing stress caused by alarming symptoms and avoiding unnecessary treatment.

Indexed as

histiocytic necrotizing lymphadenitishistopathologykikuchi-fujimoto diseaselymph node.lymphoma

Identifiers

PMID35444918
PMCPMC9009272
OpenAlexW4221073604

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.