Results 101 to 110 of about 123,589 (210)

IgA Vasculitis Presenting as Hemopericardium

CJC Open, 2023
Belfeki, Nabil, Moini, Cyrus, El Hdhili, Faten, Monchi, Mehran, Zayet, Souheil   +4 more
openaire   +2 more sources

Correlation between antiphospholipid antibodies and renal involvement in children with Henoch-Schönlein purpura: A cross-sectional study [PDF]

Caspian Journal of Internal Medicine
Background: Renal involvement is the most damaging long-term complication of Immunoglobulin-A (IgA) vasculitis. In the lack of a definite predictive biomarker for renal involvement, antiphospholipid antibodies (aPL) have been proposed in recent years ...
Mehrnoush Hassas Yeganeh, Reza Sinaei, Aye Yaraghi, Khosro Rahmani, Vadood Javadi Parvaneh, Reza Shiari, Hamid Hosseinzadeh   +6 more
doaj  

IgA Vasculitis involving four systems

, 2022
Henoch-Schonlein Purpura (HSP) is a systemic vasculitis now called IgA vasculitis, that infrequently occurs in adults. While rheumatological and gastrointestinal complications are common, lung involvement is a rare complication.
Coelho, Carolina, Lencastre Monteiro, Rita, Ghiletchi, Ângela, Diogo, Joana   +3 more
core  

Palbociclib-induced IgA vasculitis

Dermatology Online Journal, 2022
Patel, Payal M, Kelm, Ryan C, Amber, Kyle T   +2 more
openaire   +4 more sources

Vasculitis por IgA con compromiso gastrointestinal en un adolescente: Reporte de un caso y revisión de la literatura

Revista Reumatología al Día
La vasculitis por IgA es la vasculitis sistémica más frecuente en la edad pediátrica y adolescencia, caracterizada por depósito de inmunocomplejos de IgA en vasos de pequeño calibre.
Kerly Janina Cruz Mayor, José Franco Litardo   +1 more
doaj   +1 more source

Annular and Purpuric Plaques with Systemic Symptoms: A Unique Presentation of Immunoglobulin A Vasculitis

Journal of Dermatology and Dermatologic Surgery
A male in his 20s presented to the hospital with a rash, abdominal pain, blood in the stool, and fatigue. The rash, originally diagnosed as urticarial vasculitis, developed 4 months prior and had been treated with several courses of low-dose steroids ...
Rachel V. Goff, Eliana F. Zamora, Cindy Owen   +2 more
doaj   +1 more source

A Pathway to High Quality Clinical Trials in IgA Vasculitis Nephritis: Meeting Proceedings From a Multiprofessional International Collaborative Workshop [PDF]

IgA vasculitis (IgAV) is an autoimmune disease that affects the small vessels of the skin, joints, gastrointestinal (GI) tract, and kidneys. In the long term, IgAV associated with nephritis (IgAV-N) can progress to kidney failure. Evidence-based clinical
Audemard-Verger, A, Renson, Thomas, Jayne, David, King, Charlotte, Appenzeller, Simone, Bakry, R, Ozen, S, Ding, W, Wason, James, Salama, Alan, Barnes, E, Davies, Elin, Brix, Silke, Harper, L, Wade, Joshua, Trivioli, G, Smith, EMD, Pillebout, Evangéline, Jelusic, M, Bansal, Tarun, Lindsay, L, Cheung, C, Willcocks, L, Hardwick, Hayley, Williams, C, Vaglio, A, Williams, Chloe, Cheung, Chee, Pillebout, E, Beldie, MA, Keat, Karuna, Smith, R, Keat, K, Bogos, R, Peipert, J, Ding, Wen, Davies, E, Sunderkötter, Cord, Demir, Selcan, Barratt, Jonathan, O'Shaughnessy, Michelle, Sanchez-Manubens, J, Beldie, Madalina Andreea, Sanchez-Manubens, Judith, Marlais, M, Barratt, J, Bajema, I, Oni, Louise, Morgan, Henry, Alladin, A, Jayne, D, Haas, Mark, Brix, S, Hardwick, H, Hamilton, P, Marks, SD, Demir, S, Ozen, Seza, Bogos, Roxana, Appenzeller, S, Vaglio, Augusto, Gkargkoula, Panagoula, Gkargkoula, P, Jones, Caroline, Wason, J, Lindsay, Lowena, Marks, Stephen David, Trivioli, Giorgio, Pain, Clare, Chetwynd, A, Platt, C, Hafkin, Jeffrey, Jones, C, Haas, M, Alladin, Areefa, Barnes, Emily, Peipert, John, Oni, L, Chetwynd, Andrew, Willcocks, Lisa, Anastasa, Zoi, Vernon, Kelly, Brogan, P, Brogan, Paul, Sunderkötter, C, Eleftheriou, D, Bansal, T, Jelusic, Marija, Eleftheriou, Despina, Anastasa, Z, Salama, A, Audemard-Verger, Alexandra, King, C, Marlais, Matko, Bajema, Ingeborg, Pain, C, Smith, Rona, Bakry, Reima, Hafkin, J, Renson, T, Vernon, K, Hamilton, Patrick, Wade, J, Morgan, H, O'Shaughnessy, M, Platt, Caroline, Harper, Lorraine   +106 more
core   +1 more source

Glucocorticoids in IgA vasculitis

Acta Medica
IgA vasculitis (IgAV) is an immune complex vasculitis affecting small vessels characterized by IgA1 immune deposits. IgA vasculitis typically resolves spontaneously in most cases, especially in pediatric cases but may have more severe outcomes in adults and the optimal treatment for IgAV remains controversial.
openaire   +1 more source

Ultraviolet Purpura in IgA Vasculitis [PDF]

Mayo Clinic Proceedings, 2018
Daisuke, Tsukui, Hajime, Kono
openaire   +2 more sources

A Rare Case of Adult Onset IgA Vasculitis

Background: IgA vasculitis, formerly known as Henoch – Schoenlein Purpura (HSP), is vasculitis of small vessels, which is a rare and life threatening condition in adults.
Kumar, Kiran, Choudhury, Mahaswetha, Fernandes, Nathaniel, Philip, Tom   +3 more
core