Results 71 to 80 of about 10,225 (248)

Hemorrhagic Intestinal Henoch-Schonlein Purpura Complicated by Cytomegalovirus Infection

Canadian Journal of Gastroenterology, 1998
A 54-year-old man on hemodialysis for acute chronic renal failure and on corticosteroids for Henoch-Schonlein purpura developed massive hematochezia. After extensive clinical investigation, an ileal bleeding site was identified and surgically removed ...
Phong Nguyen-Ho, Laurence D Jewell, Alan BR Thomson   +2 more
doaj   +1 more source

Essential Thrombocythemia's Role in the Complex Landscape of Vasculitis: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Peripheral gangrenes have been sporadically documented as the initial presentation of essential thrombocythemia (ET), as exemplified in the preceding case reports. Nevertheless, the prevalence of vasculitis‐induced skin problems as the primary indication of ET has not been extensively examined.
Mohammad Reza Jafari Nakhjavani, Seyedeh‐Tarlan Mirzohreh, Sousan Kolahi, Mehrzad Hajialilo, Mehdi Jafarpour, Arezou Ghassembaglou, Mir Ali Sattary Oskouie, Tala Pourlak, Sepideh Tahsini Tekantapeh   +8 more
wiley   +1 more source

EFEKTIFITAS PENERAPAN TERAPI MUROTTAL PADA PASIEN HENOCH SCHUELEIN PURPURA NEFRITIS (HSPN) DENGAN MASALAH KEPERAWATAN NYERI AKUT DI RUANG MELATI RSI JEMURSARI SURABAYA [PDF]

, 2016
Henoch Schonlein Purpura Nefritis (HSPN) merupakan suatu vaskulitis sistemik yang terjadi melalui mekanisme imunologik dengan salah satu gejalanya adalah nyeri persendian dan nyeri abdomen.
LUKITANINGSIH, WIDIYA
core  

The Association of RNase L, Cytokines, and Chemokines With Severity of Multisystem Inflammatory Syndrome in Children

Journal of Medical Virology, Volume 97, Issue 10, October 2025.
ABSTRACT The 2′,5′‐oligoadenylate synthetase (OAS)‐ribonuclease L (RNase L) system, induced by type I interferons, defends against RNA viruses. Inborn errors in this pathway may trigger inflammatory cytokines, contributing to SARS‐CoV‐2‐related multisystem inflammatory syndrome in children (MIS‐C).
Ting‐Yu Yen, Chia‐Lang Hsu, Chun‐Yi Lu, Ni‐Chung Lee, Ming‐Tai Lin, Kuan‐Ying Arthur Huang, Boon Fatt Tan, Tu‐Hsuan Chang, Chun‐Min Kang, Wei‐Shiung Yang, Bor‐Luen Chiang, Li‐Min Huang, Hsin‐Hui Yu, Luan‐Yin Chang   +13 more
wiley   +1 more source

Koebner phenomenon in leukocytoclastic vasculitis: A case report and an updated review of the literature

SAGE Open Medical Case Reports, 2019
Leukocytoclastic vasculitis is the most common form of cutaneous vasculitis. It is a neutrophilic small vessel vasculitis resulting from the deposition of circulating immune complexes.
Farah Kassam, Sabrina Nurmohamed, Richard M Haber   +2 more
doaj   +1 more source

IgA Vasculitis Across the Ages: Is It Time for a Precision Medicine Approach?

ACR Open Rheumatology, Volume 7, Issue 9, September 2025.
IgA vasculitis (IgAV; formerly Henoch‐Schönlein purpura) is a systemic small vessel vasculitis most commonly affecting the skin, gut, joints, and kidneys. Nephritis is the most concerning complication for all ages because it carries the risk of progression to irreversible end‐stage kidney failure.
A. Gage, R. J. Pepper, J. Marro, A. D. Salama, L. Oni   +4 more
wiley   +1 more source

Henoch-Schönlein purpura in an older man presenting as rectal bleeding and IgA mesangioproliferative glomerulonephritis: a case report

Journal of Medical Case Reports, 2011
Introduction Henoch-Schönlein purpura is the most common systemic vasculitis in children. Typical presentations are palpable purpura, abdominal pain, arthritis, and hematuria.
Howarth Charles B, Jirajariyavej Teeranun, Cheungpasitporn Wisit, Rosen Raquel M   +3 more
doaj   +1 more source

Acute compartment syndrome of the hand in Henoch-Schonlein Purpura [PDF]

, 2007
An eight year old boy with Henoch-Schonlein Purpura (HSP) presented with acute compartment syndrome (ACS) of his left hand following arterial cannulation of his radial artery in intensive care unit.
C Martin, D Lawes, Eng-Seng Ng, Guntur E Luis, J Ronkainen, J Sandell, JA Mills, NN Al-Harbi, RN Ma'luf, T Imai, TT Wu   +10 more
core   +3 more sources

Acute Post‐Streptococcal Glomerulonephritis in a 22‐Month‐Old Toddler: A Rare and Uncustomary Age of Onset

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Acute post‐streptococcal glomerulonephritis (APSGN) is an important immunological complication that follows Group A Streptococcus (GAS) infections. It usually affects children between 5 and 15 years of age and is rarely seen in children younger than 3 years, likely because their immature immune systems limit the exaggerated immune response ...
Abrham Bire Akeberegn, Amanuel Anegagregn Bizuneh   +1 more
wiley   +1 more source

Henoch-Schönlein Purpura Nephritis in Childhood [PDF]

, 2011
An Update on Glomerulopathies - Clinical and Treatment Aspects is a systemic overview of recent advances in clinical aspects and therapeutic options in major syndromes of glomerular pathology.
Marco Zaffanello
core   +2 more sources