Results 1 to 10 of about 201,611 (277)

Scurvy masquerading as IgA vasculitis. [PDF]

Pediatr Rheumatol Online J
Abstract Background 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, autism spectrum disorder, and physical ...
Kassa HL, Singh S, Douglas-Jones M, Schermbrucker G, De Lange J, Phoya F, Butters C, Hlela C, Coetzee A, Banderker E, Webb K.   +10 more
europepmc   +5 more sources

IgA nephropathy with leucocytoclastic vasculitis [PDF]

Journal of International Medical Research, 2018
Leucocytoclastic vasculitis is a rare type of allergic disease caused by immune complexes. IgA nephropathy is a glomerulopathy characterized by recurrent episodes of gross haematuria or microscopic haematuria and IgA deposition in the glomerular mesangial region. IgA nephropathy complicating leucocytoclastic vasculitis is rare documented. We present a
Lin-Yan Wei, Ya-Li Zhang, Chao Liu, Guoliang Li   +3 more
openaire   +3 more sources

Food-induced IgA Vasculitis (Henoch-Schönlein Purpura) [PDF]

European Journal of Case Reports in Internal Medicine, 2017
Immunoglobulin A (IgA) vasculitis is a rare entity in adults. It can be triggered by allergens such as drugs, food, or insect bites. We present a case of an adult male with a cutaneous IgA vasculitis of palpable purpura after eating canned ...
Acebes Repiso, Gonzalo, Bautista Alonso, Rosa Eva, García Bruñén, José Miguel, Martínez González, Ana, Moreno Díaz, Javier   +4 more
core   +14 more sources

Intermittent abdominal pain in IgA vasculitis [PDF]

Revista Paulista de Pediatria, 2022
ABSTRACT Objective: To assess intermittent abdominal pain in IgA vasculitis patients and its relation to demographic data, clinical manifestations and treatments. Methods: A retrospective cohort study included 322 patients with IgA vasculitis (EULAR/PRINTO/PRES criteria) seen at the Pediatric Rheumatology Unit in the last 32 years.
Izabel Mantovani Buscatti, Juliana Russo Simon, Vivianne Saraiva Leitao Viana, Tamima Mohamad Abou Arabi, Vitor Cavalcanti Trindade, Ana Carolina Cortez Maia, Lara Regina Cavalcante Melo, Bianca Pires Ihara, Nadia Emi Aikawa, Clovis Artur Silva   +9 more
openaire   +7 more sources

IgA Vasculitis and IgA Nephropathy: Same Disease? [PDF]

Journal of Clinical Medicine, 2021
Many authors suggested that IgA Vasculitis (IgAV) and IgA Nephropathy (IgAN) would be two clinical manifestations of the same disease; in particular, that IgAV would be the systemic form of the IgAN. A limited number of studies have included sufficient children or adults with IgAN or IgAV (with or without nephropathy) and followed long enough to ...
É. Pillebout
openaire   +4 more sources

Fasciitis as a Complication of IgA Vasculitis. [PDF]

Cureus
Immunoglobulin A vasculitis (IgAV) is a systemic small-vessel vasculitis caused by the deposition of IgA-based immune complexes, with myalgia being a rare complication. This study reports a pediatric case of IgAV with fasciitis. A five-year-old boy with no previous medical history was admitted to the hospital with abdominal pain and repeated bilious ...
Nii K, Kondo Y, Okamoto N, Yamamoto M, Kusaka T.   +4 more
europepmc   +3 more sources

Annular Leukocytoclastic Vasculitis: A New Feature of IgA Vasculitis. [PDF]

Eur J Case Rep Intern Med
Background: Annular erythema is a rare manifestation of leukocytoclastic vasculitis. It may be associated with various drugs, infections, malignancies, or systemic diseases. Case description: A 36-year-old woman with no personal medical history presented with annular erythema with target lesions and petechial purpura.
Belfeki N, Ghriss N, Kammoun S, Zayet S, Moini C, Terrier B.   +5 more
europepmc   +4 more sources

Exploring the Diagnostic Odyssey of IgA Vasculitis. [PDF]

Cureus
IgA vasculitis is a form of small vessel vasculitis characterized by IgA immune complex deposition. Although primarily affecting children, it can also occur in adults, often with more severe manifestations and a higher risk of chronic kidney disease (CKD). The authors present the case of a 77-year-old man with significant cardiovascular risk and atrial
Rosmaninho I, Simão-Parreira B, Leal C, Cardoso L, Almeida J.   +4 more
europepmc   +3 more sources

Renal biopsy in children with IgA vasculitis [PDF]

Brazilian Journal of Nephrology, 2022
Abstract Introduction Henoch-Schönlein purpura nephritis (HSN) is defined as Henoch-Schönlein purpura with kidney involvement, including hematuria and/or proteinuria. The aim of this study was to evaluate the data of HSN patients who underwent renal biopsy, and compare the main clinical and laboratory parameters that may affect renal biopsy findings ...
Mehtap Akbalik Kara, Beltinge Demircioğlu Kiliç, Mithat Büyükçelik, Ayşe Balat   +3 more
openaire   +6 more sources

A Case of Henoch-Schonlein Purpura Associated with Rotavirus Infection in an Elderly Asian Male and Review of the Literature. [PDF]

, 2017
BACKGROUND Henoch-Schönlein purpura (HSP), a small vessel vasculitis mediated by deposition of immune-complexes containing IgA in the skin, gut, and glomeruli, often presents with abdominal pain, purpuric rash in the lower extremities and buttocks, joint
Adderley, Adderley, Bender, Epstein, Homberg, Kim, Mongillo, Page, Raja Beharelle, Ridding, Saur, Szaflarski, Wade, Zaccolo   +13 more
core   +2 more sources