Results 51 to 60 of about 203,606 (241)

IgA (Henoch Schönlein Purpura) Vasculitis in a Pediatric Patient with COVID-19 and Strongyloidiasis

Revista de la Facultad de Medicina Humana, 2021
Vasculitis is a rare disease in children, with IgA Vasculitis being its most common presentation. One condition that has been associated with the development of vasculitis is the invasion of the vascular endothelium by Strongyloides stercoralis in cases ...
Mayron David Nakandakari Gomez, Hamilton Marín Macedo, Raúl Seminario Vilca   +2 more
doaj   +1 more source

New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]

, 1984
The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter, Kessler, C., Krause, Klaus-Henning, Reuther, R.   +3 more
core   +1 more source

New Insights and Challenges Associated With IgA Vasculitis and IgA Vasculitis With Nephritis—Is It Time to Change the Paradigm of the Most Common Systemic Vasculitis in Childhood?

Frontiers in Pediatrics, 2022
What are the challenges ahead and how have we responded so far when it comes to the non-granulomatous systemic vasculitis, characterized mainly by deposits of IgA immune complexes in the endothelium of small blood vessels—IgA vasculitis (IgAV)?
M. Jelušić, M. Šestan, T. Giani, R. Cimaz   +3 more
semanticscholar   +1 more source

Vasculitis IgA en el adulto. Informe de caso

Medisur, 2021
La vasculitis IgA, también conocida como púrpura de Schönlein-Henoch, es una vasculitis leucocitoclástica que involucra pequeños vasos con depósito de inmunocomplejos IgA. Puede abarcar piel, articulaciones, riñones y tracto gastrointestinal.
Samuel Sánchez Sánchez, Ana Laura Navarro Baldellot, Ernesto A. López Sotolongo   +2 more
doaj  

Pauci-immune glomerulonephritis in individuals with disease associated with levamisole-adulterated cocaine: a series of 4 cases. [PDF]

, 2014
Exposure to levamisole-adulterated cocaine can induce a distinct clinical syndrome characterized by retiform purpura and/or agranulocytosis accompanied by an unusual constellation of serologic abnormalities including antiphospholipid antibodies, lupus ...
Butcher, Brad, Carlson, Adam Q, Graf, Jonathan, Imboden, John B, Jen, Kuang-Yu, Sam, Ramin, Tuot, Delphine S   +6 more
core   +2 more sources

Systemic Activation of Neutrophils by Immune Complexes Is Critical to IgA Vasculitis

Journal of Immunology, 2022
In IgA vasculitis (IgAV) perivascular deposition of IgA1 immune complexes (IgA-ICs) is traditionally considered the fundamental trigger for polymorphonuclear neutrophil (PMN)–mediated damage.
Sarah Mayer-Hain, Kathleen Gebhardt, M. Neufeld, J. Ehrchen, K. Molyneux, J. Barratt, Eva Nattkemper, Dennis Gerloff, J. Roth, T. Vogl, K. I. Pappelbaum, C. Sunderkötter   +11 more
semanticscholar   +1 more source

Vasculitis and familial Mediterranean fever: Description of 22 French adults from the juvenile inflammatory rheumatism cohort

Frontiers in Medicine, 2022
ObjectiveThe frequency of vasculitis may be increased in patients with Familial Mediterranean Fever (FMF), according to several studies. Our aim was to assess the characteristics of French adult patients with both diseases.MethodsPatients with vasculitis
Salam Abbara, Jean-Benoit Monfort, Léa Savey, Philippe Moguelet, David Saadoun, Claude Bachmeyer, Olivier Fain, Benjamin Terrier, Zahir Amoura, Alexis Mathian, Laurent Gilardin, David Buob, Chantal Job-Deslandre, Jean-François Dufour, Rebecca Sberro-Soussan, Gilles Grateau, Sophie Georgin-Lavialle, Sophie Georgin-Lavialle   +17 more
doaj   +1 more source

IgA Vasculitis Followed by IgA Nephropathy Without an Identifiable Trigger: The Same Disease or a Spectrum of Related Conditions?

Cureus, 2023
IgA vasculitis and IgA nephropathy are characterized by IgA deposition in blood vessels and glomerular mesangium, respectively. The former is far more common in the pediatric population, while the latter presents more often in adulthood.
Rebecca Lapides, Juan Crespo-Quezada, Teena Thomas, Felipe Carmona Pires, Gagandeep Chera   +4 more
semanticscholar   +1 more source

Drug-Induced IgA Vasculitis in an Adult

Cureus, 2023
A 65-year-old man developed palpable purpuric papules and plaques on his lower extremities, which quickly spread to his trunk and upper extremity after being prescribed cephalexin and doxycycline in the emergency room.
Miranda Yousif, N. H. Vigil, Rui Haddad
semanticscholar   +1 more source

Acute Hemorrhagic Edema of Infancy [PDF]

, 2016
Acute Hemorrhagic Edema of Infancy is a small vessel leucocytoclastic vasculitis affecting young infants. It is characterized by large, target-like, macular to purpuric plaques predominantly affecting the face, ear lobes and extremities.
Amaro, C, Garcia, C, Sokolova, A, Torre, ML   +3 more
core   +1 more source