Evidence map›Paper›PMID 36445270›Full record

ArticleJournal of cutaneous pathology2022

The mixed spongiotic and interface reaction pattern: A study of clinical and histopathologic findings.

Madison Ernst, Mia Lundgren, Michael D Evans, Daniel Miller, Alessio Giubellino

Open access · hybridAbstract read
In one paragraph

Article in Journal of cutaneous pathology, 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
0.9field-weighted citation impact, top 27% 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. Review
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  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 1 institution in 1 country.

Madison ErnstDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.ORCID https://orcid.org/0000-0002-8480-6436
Mia LundgrenDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.
Michael D EvansClinical and Translational Science Institute, University of Minnesota, Minneapolis, Minnesota, USA.
Daniel MillerDepartment of Dermatology, University of Minnesota, Minneapolis, Minnesota, USA.ORCID https://orcid.org/0000-0002-4931-9528
Alessio GiubellinoDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.ORCID https://orcid.org/0000-0002-5352-0662
University of Minnesota · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
National Institutes of Health's National Center for Advancing Translational Sciences UL1TR002494NCATS NIH HHS UL1 TR002494
6 · The paper itself

Abstract

backgroundCategorization of biopsy specimens into inflammatory reaction patterns is central to dermatopathologic assessment. Mixed inflammatory patterns are poorly characterized and may represent clinicopathologic challenges. The purpose of this study was to identify clinical and histopathologic findings associated with the mixed spongiotic-interface dermatitis (SID) histopathologic pattern.

methodsFifty-one institutional biopsy specimens of SID were identified over a 2-year period by retrospective natural language search. Histopathologic and clinical features were identified.

resultsThe most common histopathologic features associated with SID were mild spongiosis (51%), focal vacuolar interface change (72%), lymphocytic exocytosis (92%), and superficial-dermal lymphocytic infiltrate (94%) with variable eosinophils (61%). Clinically, 80% of subjects presented with a symmetric morbilliform eruption. Polypharmacy (94%), immunosuppression (47%), and history of malignancy (47%) were common. The most common diagnoses were drug reaction (37%), possible drug reaction (12%), and viral exanthem (12%). Drug reaction with eosinophilia and systemic symptoms represented 25% of all confirmed cutaneous adverse drug reactions (CADR). Average time from drug initiation to symptom initiation was 20 days (SD: 22.3, range: 0-90); median disease duration was 25.5 days. Spongiotic vesicles and Langerhans cells were less common in patients with a strong clinicopathologic diagnosis of drug reaction compared to non-drug eruptions (p = 0.04).

conclusionsThe mixed SID pattern is commonly encountered in CADR but may represent a more subacute course, implying consideration for inciting medication(s) started before the typical 7- to 14-day window.

Indexed as

EczemaDrug-Related Side Effects and Adverse ReactionsHumansInflammationRetrospective Studiesdermatopathologydrug eruptionsdrug reaction with eosinophilia and systemic symptomsinterfacemaculopapular eruptionspongiotic

Identifiers

PMID36445270
PMCPMC9709294
OpenAlexW4289731724

What OpenQuestion holds

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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.