Evidence map›Paper›PMID 32779733›Full record

ArticleThe British journal of dermatology2021

The differing pathophysiologies that underlie COVID-19-associated perniosis and thrombotic retiform purpura: a case series.

C M Magro, J J Mulvey, J Laurence, S Sanders, A N Crowson, M Grossman, J Harp, G Nuovo

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The British journal of dermatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
14.8field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 105 citations in OpenAlex.

  1. Pooled it
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  11. Part II: Cutaneous manifestations of peripheral vascular disease.Journal of the American Academy of Dermatology · 2023
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  20. Insights into urticaria in pediatric and adult populations and its management with fexofenadine hydrochloride.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 1 country.

C M MagroDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
J J MulveyDepartment of Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
J LaurenceDepartment of Medicine, Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY, USA.
S SandersSanders Dermatology, New City, NY, USA.
A N CrowsonRegional Medical Laboratories, Pathology Laboratory Associates and University of Oklahoma, Tulsa, OK, USA.
M GrossmanDepartment of Dermatology, Yale University, New Haven, CT and Hofstra/Northwell, New Hyde, NY, USA.
J HarpDepartment of Dermatology, Weill Cornell Medicine, New York, NY, USA.
G NuovoThe Ohio State University Comprehensive Cancer Center, Columbus Ohio and Discovery Life Sciences, Powell, OH, USA.
Cornell University · USMemorial Sloan Kettering Cancer Center · USThe Ohio State University · USUniversity of Oklahoma · USWeill Cornell Medicine · USYale University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundThere are two distinctive acral manifestations of COVID-19 embodying disparate clinical phenotypes. One is perniosis occurring in mildly symptomatic patients, typically children and young adults; the second is the thrombotic retiform purpura of critically ill adults with COVID-19.

objectivesTo compare the clinical and pathological profiles of these two different cutaneous manifestations of COVID-19.

methodsWe compared the light microscopic, phenotypic, cytokine and SARS-CoV-2 protein and RNA profiles of COVID-19-associated perniosis with that of thrombotic retiform purpura in critical patients with COVID-19.

resultsBiopsies of COVID-19-associated perniosis exhibited vasocentric and eccrinotropic T-cell- and monocyte-derived CD11c

conclusionsCOVID-19-associated perniosis represents a virally triggered exaggerated immune reaction with significant type I interferon signaling. This is important to SARS-CoV-2 eradication and has implications in regards to a more generalized highly inflammatory response. We hypothesize that in the thrombotic retiform purpura of critically ill patients with COVID-19, the vascular thrombosis in the skin and other organ systems is associated with a minimal interferon response. This allows excessive viral replication with release of viral proteins that localize to extrapulmonary endothelium and trigger extensive complement activation.

Indexed as

AdolescentAgedAge FactorsBiopsyCaspase 3ChilblainsCOVID-19Diagnosis, DifferentialFemaleFootHandHumansInterferon Type IInterleukin-6Livedo ReticularisMaleCASP3 protein, humanCaspase 3IL6 protein, humanInterferon Type IInterleukin-6MX1 protein, humanMyxovirus Resistance ProteinsRNA, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID32779733
PMCPMC7405151
OpenAlexW3044513554

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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.