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- Title
IgA vasculitis.
- Authors
Tadokoro, T; Abe, T; Nakano, T; Kimura, Y; Higaki, K; Hayashidani, S; Tashiro, H
- Abstract
Complement component 3 (C3) and IgA depositions were observed in the vessel walls (Figure 1d and e), confirming IgA vasculitis. Therefore, clinicians should consider IgA vasculitis even in adults if they notice palpable purpura and abdominal pain. Also has a high recurrence rate of 32%, despite typically having a good prognosis.[2] If is generalized as a childhood disease, it may be overlooked during differential diagnosis.
- Subjects
IMMUNOGLOBULIN A; COMPLEMENT (Immunology); SCHOENLEIN-Henoch purpura; VASCULITIS
- Publication
QJM: An International Journal of Medicine, 2023, Vol 116, Issue 7, p538
- ISSN
1460-2725
- Publication type
Article
- DOI
10.1093/qjmed/hcad038