IgA vasculitis after COVID-19: a case-based review.

IgA vasculitis after COVID-19: a case-based review.

Publication date: Jul 01, 2024

IgA-associated vasculitis (IgAV) known as Henoch – SchcF6nlein purpura (HSP) disease is an inflammatory disorder of small blood vessels. It’s the most common type of systemic vasculitis in children which can be associated with the inflammatory process following infections. IgA vasculitis is a rare and poorly understood systemic vasculitis in adults. Coronavirus disease 2019 (COVID-19) has been associated with HSP in both adults and children. A 58-year-old woman was diagnosed with HSP, fulfilling the clinical criteria: palpable purpura, arthritis, hematuria. The disclosure of the HSP disease was preceded by a infection of the respiratory tract. COVID-19 infection was confirmed via the presence of IgM and IgG antibodies. This case indicates the possible role of SARS-CoV-2 in the development of HSP. The clinical course of IgAV in adults appears to be different from pediatric IgAV, especially due to higher risk of renal complications. Symptoms of the disease quickly resolved with low-dose of steroids.

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Concepts Keywords
Antibodies COVID-19
Coronavirus COVID-19
Old Female
Pediatric Henoch-Schönlein purpura
Woman Humans
IgA Vasculitis
IgA vasculitis
Immunoglobulin A
Immunoglobulin A
Middle Aged
Palpable purpura
Prognosis
SARS-CoV-2

Semantics

Type Source Name
disease MESH IgA vasculitis
disease MESH COVID-19
disease MESH vasculitis
disease MESH purpura
disease MESH systemic vasculitis
disease IDO process
disease MESH infections
disease MESH arthritis
disease MESH hematuria
disease IDO infection
disease MESH clinical course
disease MESH complications
disease VO dose

Original Article

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