Results 11 to 20 of about 220,566 (226)
Scurvy masquerading as IgA vasculitis
Vitamin C deficiency, or scurvy, is rare but poses risks for children with poor diets, limited resources, or malabsorption issues. It may also be common in children with restrictive or selective dietary habits in children with global developmental delay,
H. L. Kassa +11 more
semanticscholar +4 more sources
Navigating the initial diagnosis and management of adult IgA vasculitis: A reviewCapsule Summary
Background: IgA vasculitis in adults has not been thoroughly studied. This has left a practice gap related to the management and follow-up of a population that is at an increased risk of comorbidities and potentially poor outcomes. For this reason, it is
Brenna G. Kelly, BA +5 more
doaj +2 more sources
IgA vasculitis associated with chronic myelomonocytic leukemia [PDF]
IgA vasculitis is a predominantly pediatric autoimmune disease characterized by IgA deposit in small vessels. Chronic myelomonocytic leukemia (CMML) is a rare hematological malignancy classified within myelodysplastic syndromes.
Bénédicte Rouvière +6 more
doaj +2 more sources
Annular Leukocytoclastic Vasculitis: A New Feature of IgA Vasculitis
Background Annular erythema is a rare manifestation of leukocytoclastic vasculitis. It may be associated with various drugs, infections, malignancies, or systemic diseases.
N. Belfeki +5 more
semanticscholar +4 more sources
Immunoglobulin A vasculitis induced by atypical pneumonia infection with Chlamydophila pneumonia
Infections are a common trigger for IgA vasculitis. Among the bacteria that cause atypical pneumonia, Mycoplasma pneumoniae infection has strongly been associated with IgA vasculitis, with Chlamydophila pneumoniae reported with IgA vasculitis in only one
Seung Ah Kang +2 more
doaj +1 more source
Background Immunoglobulin A vasculitis (IgA vasculitis) is one of the most common forms of vasculitis in children. It rarely occurs in adults. It is a systemic vasculitis with IgA deposition and is characterized by the classical tetrad of purpura ...
Hanui Park, Miji Lee, Jin Seon Jeong
doaj +1 more source
Treatment of refractory IgA vasculitis with dapsone: a systematic review [PDF]
IgA vasculitis, formerly known as Henoch-Schönlein purpura, is a systemic IgA-mediated vasculitis of the small vessels commonly seen in children. The natural history of IgA vasculitis is generally self-limiting; however, one-third of patients experience ...
Keum Hwa Lee +11 more
doaj +1 more source
A Child with Immunoglobulin A Vasculitis and Hemorrhagic Shock: An Unusual Presentation
Immunoglobulin A (IgA) vasculitis, formerly known as Henoch–Schonlein purpura, is the most common vasculitis in children affecting small-sized vessels. Although IgA vasculitis is a self-limiting disease, a small number of patients can present with severe
Shahad Alansari, Alhanouf Alsaleem
doaj +1 more source
Cutaneous IgA vasculitis triggered by acetaminophen. [PDF]
Gaspar de Alba J +4 more
europepmc +4 more sources
Low Back Pain and Swelling as an Atypical Presentation of IgA Vasculitis
Introduction: Immunoglobulin A vasculitis (IgA vasculitis), formerly Henoch-Schonlein purpura, is the most common vasculitis in children. Case Report: A 6-year-old female presented with low back pain and swelling, difficulty ambulating, and rash two ...
Clay T. Winkler +2 more
doaj +1 more source

