ArticleCureus2026
A Case of Henoch-Schönlein Purpura in a Returning Traveler.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
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Who cites it
0 citing papers in PubMed.
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
IgA vasculitis, formerly known as Henoch-Schönlein purpura, is an immune complex-mediated small-vessel vasculitis that primarily affects children but may occur in adults, where it carries a higher risk of systemic complications, particularly renal involvement. Adult-onset disease is frequently underrecognized and may lack classic features, instead mimicking infectious, autoimmune, or drug-related conditions, thereby delaying diagnosis. In patients with persistent purpura and an unrevealing initial workup, vasculitis should remain in the differential diagnosis. We present the case of a patient diagnosed with IgA vasculitis following recent international travel, highlighting the diagnostic challenges and clinical reasoning that ultimately led to the diagnosis.
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Registered trials
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.