Evidence map›Paper›PMID 40026936›Full record

ArticleCureus2025

Hypocomplementemic Urticarial Vasculitis Syndrome: A Rare Form of Vasculitis.

Saurabh Kumar Singh, Mohit Gupta, Shilpi Rani, Pratap Singh

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Saurabh Kumar SinghCardiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, IND.
Mohit GuptaCardiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, IND.
Shilpi RaniInternal Medicine, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, IND.
Pratap SinghInternal Medicine, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare autoimmune disorder characterized by recurrent urticarial lesions and acquired hypocomplementemia with systemic manifestations. Systemic involvement can either be present at the onset of disease or develop later. Here, we present a rare case of a 22-year-old female, who initially presented with generalized rash and was eventually diagnosed with HUVS. She responded well to dapsone. This article emphasizes the importance of a comprehensive review of systemic manifestations accompanying urticaria.

Indexed as

dapsonehypocomplementemic urticarial vasculitis syndromeurticariavasculitisyoung female patient

Identifiers

PMID40026936
PMCPMC11871547

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.