Evidence map›Paper›PMID 36451638›Full record

ArticleCureus2022

A Rare Case of a Child Diagnosed With Multisystem Inflammatory Syndrome After COVID-19 Presenting With Renal Infarctions and Transient Blast Cells: A Case Report and Literature Review.

Mohammed A Almatrafi, Abdulrahman F Kabli, Yara Subahi, Esraa Yaseen, Nouf Alsahaf, Dhuha Alidrisi, Hanan A Ahmed, Hassan M Masmali, Ossamah Alahmad, Mohammad N Khan and 1 more

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, 1 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

11 authors at 3 institutions in 1 country.

Mohammed A AlmatrafiDepartment of Pediatrics, Umm Al-Qura University, Makkah, SAU.
Abdulrahman F KabliDepartment of Medicine, Umm Al-Qura University, Makkah, SAU.
Yara SubahiDepartment of Pediatrics, Security Forces Hospital, Makkah, SAU.
Esraa YaseenDepartment of Medicine, Umm Al-Qura University, Makkah, SAU.
Nouf AlsahafDepartment of Pediatrics, Umm Al-Qura University, Makkah, SAU.
Dhuha AlidrisiDepartment of Pediatrics, Security Forces Hospital, Makkah, SAU.
Hanan A AhmedDepartment of Pediatrics, Security Forces Hospital, Makkah, SAU.
Hassan M MasmaliDepartment of Pediatrics, Maternity and Children Hospital, Makkah, SAU.
Ossamah AlahmadDepartment of Pediatrics, Security Forces Hospital, Makkah, SAU.
Mohammad N KhanDepartment of Pediatrics, Umm Al-Qura University, Makkah, SAU.
Faisal MinshawiDepartment of Laboratory Medicine, Umm Al-Qura University, Makkah, SAU.
Maternity and Children's Hospital · SASecurity Forces Hospital · SAUmm al-Qura University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multisystem inflammatory syndrome in children (MIS-C) can develop weeks after the Coronavirus disease 2019 (COVID-19). The disease's clinical spectrum includes persistent febrile illness, features resembling Kawasaki disease, and cytokine storm symptoms. In severe cases, multisystem organ failure and death may result if not treated promptly. This report discusses a rare case of a 13-year-old girl presenting with fever and acute kidney injury (AKI) eight weeks after recovering from COVID-19 who was diagnosed with MIS-C. A 13-year-old female presented with a fever and abdominal pain following a recent COVID-19. A physical examination revealed a febrile, ill-looking child with abdominal tenderness. Pancytopenia, transaminitis, AKI, and a hyperinflammatory state were noted in the initial laboratory workup. Furthermore, blast cells were seen on the peripheral blood smear. Despite appropriate empiric antibiotic therapy for sepsis, she did not show signs of clinical improvement. An abdominal computed tomography (CT) scan revealed multiple focal areas of hypoattenuating lesions involving both kidneys, suggestive of bilateral renal infarction. Since she met the criteria of the Centers for Disease Control and Prevention (CDC) for MIS-C diagnosis, a high dose of intravenous immunoglobulin (IVIG) led to a dramatic improvement in the patient's condition and complete recovery from her illness. This case report describes a rare clinical presentation of MIS-C in a child who presented with AKI due to presumably thrombotic events and transient blast cells in blood film secondary to a severe inflammatory process. Further studies are needed to determine the prevalence of thrombotic AKI associated with MIS-C.

Indexed as

acute renal injuryblast cellcovid-19 virus infectionpediatric inflammatory multisystem syndromesars-cov-2 infection

Identifiers

PMID36451638
PMCPMC9703834
OpenAlexW4307532162

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.