Evidence map›Paper›PMID 41479738›Full record

ArticleWorld journal of clinical cases2025

Systemic and dermatological findings of immunoglobulin A vasculitis in a black child: A case report.

Khulud Mahmood Nurani, Gloria Natalia, Najib Kadernani, Khalid Kadernani

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Article in World journal of clinical cases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Khulud Mahmood NuraniSchool of Medicine, University of Nairobi, Nairobi 30197-00100, Nairobi City, Kenya.
Gloria NataliaSchool of Medicine, University of Nairobi, Nairobi 30197-00100, Nairobi City, Kenya.
Najib KadernaniSchool of Medicine, University of Nairobi, Nairobi 30197-00100, Nairobi City, Kenya. najib.ayub14@gmail.com.
Khalid KadernaniDepartment of Medicine, Nairobi West Hospital, Nairobi 19676 - 00100, Nairobi City, Kenya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunoglobulin A (IgA) vasculitis, formerly known as Henoch-Schönlein purpura, is a small vessel vasculitis predominantly affecting children. It commonly presents with a triad of purpuric rash, arthralgia, and abdominal pain. However, dermatologic manifestations of IgA vasculitis in black-skinned individuals are poorly documented in literature. CASE SUMMARY: This case report describes an 11-year-old black girl with acute onset of rash, joint pain, and abdominal pain, subsequently diagnosed with IgA vasculitis.

conclusionThe case highlights the importance of early recognition and supportive management in ensuring a favorable outcome, particularly in dark-skinned populations.

Indexed as

Abdominal painArthralgiaBlack-skinnedCase reportDermatologic findingsHenoch-Schönlein purpuraImmunoglobulin A vasculitisPediatric vasculitisPurpura

Identifiers

PMID41479738
PMCPMC12754126

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