Evidence map›Paper›PMID 35655625›Full record

ArticleJournal of medical cases2022

A One-Year-Old Girl With Human Parvovirus B19 Infection and Hypocomplementemia Mimicking Incomplete Kawasaki Disease.

Kazumi Oura, Shinichi Ishikawa, Haruki Shiraishi, Yuji Maruo, Norio Sato, Takashi Suganuma, Makoto Mikawa, Tomonobu Sato

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

Article in Journal of medical cases, 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 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, 2 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

8 authors at 3 institutions in 3 countries.

Kazumi OuraDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Shinichi IshikawaDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Haruki ShiraishiDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Yuji MaruoDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Norio SatoDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Takashi SuganumaDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Makoto MikawaDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Tomonobu SatoDepartment of Pediatrics, Kitami Red Cross Hospital, Kitami, Hokkaido 090-8666, Japan.
Japanese Red Cross Hokkaido College of Nursing · JPKrankenhaus vom Roten Kreuz · DERed Cross Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human parvovirus B19 (B19) is a single-stranded DNA virus that targets erythroid progenitor cells in the bone marrow. B19 causes erythema infectiosum in children, transient aplastic anemia, pure red cell aplasia, hydrops fetalis, and contributes to other illnesses. An association between B19 infection and hypocomplementemia and rheumatoid arthritis has been reported, but the underlying mechanisms remain unclear. We report the case of a 1-year-old Japanese girl with persistent fever, skin rash, transient edema of the extremities, hypoalbuminemia, and hypocomplementemia associated with B19 infection. We considered Kawasaki disease (KD) and collagen diseases, particularly systemic lupus erythematosus, in our differential diagnosis. B19 infection might be associated with serological features that suggest systemic lupus erythematosus and may present with clinical symptoms seen in KD. Especially during erythema infectiosum epidemics, we must consider B19 infection in the differential diagnosis of KD patients who demonstrate atypical clinical symptoms and unexplained laboratory findings.

Indexed as

Erythema infectiosumHuman parvovirus B19HypocomplementemiaKawasaki diseaseSystemic lupus erythematosus

Identifiers

PMID35655625
PMCPMC9119372
OpenAlexW4229334328

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.