Results 11 to 20 of about 22,409 (253)

A Case of Polyarteritis Nodosa Associated with Vertebral Artery Vasculitis Treated Successfully with Tocilizumab and Cyclophosphamide

open access: yesCase Reports in Pediatrics, 2016
Pediatric polyarteritis nodosa is rare systemic necrotizing arteritis involving small- and medium-sized muscular arteries characterized by aneurysmal dilatations involving the vessel wall.
Kae Watanabe   +2 more
doaj   +3 more sources

Polyarteritis Nodosa

open access: yesCurrent Opinion in Pediatrics, 2022
Dr.
Andrew G. Lee, MD
core   +3 more sources

Pericarditis of Polyarteritis Nodosa. [PDF]

open access: yesCureus, 2023
Polyarteritis nodosa (PAN) is a rare systemic vasculitis characterised by necrotising inflammation of medium-sized arteries. PAN can affect patients of any age, gender, or ethnic background.
Ambrogetti R   +4 more
europepmc   +4 more sources

Polyarteritis Nodosa [PDF]

open access: yesTechniques in Vascular and Interventional Radiology, 2014
The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a pathologist at the University of Vienna. The initial report describes a 23-year-old man who had a 5-day history of fever and diarrhea. Since then, the definition of PAN
Misra, Sanjay   +3 more
core   +3 more sources

Cutaneous polyarteritis nodosa [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
Polyarteritis nodosa is a rare vasculitis in children characterized by necrotizing inflammation in small and medium size arteries. It is classified into systemic and cutaneous PAN according to the presence of systemic symptoms or visceral involvement. We
María Alejandra Matteoda   +5 more
doaj   +5 more sources

Cutaneous polyarteritis nodosa: Diagnosis lies skin deep

open access: yesIndian Journal of Paediatric Dermatology, 2018
Cutaneous polyarteritis nodosa (CPAN) is an uncommon form of cutaneous vasculitis. Definitive diagnosis is based on skin biopsy. We present a rare case of CPAN in a 2-year-old male child who presented with a history of fever, cutaneous ulcers, and ...
Raghavendraswami Amoghimath   +3 more
doaj   +2 more sources

Systematic review of childhood-onset polyarteritis nodosa and DADA2

open access: yesSeminars in Arthritis & Rheumatism, 2021
Background: Diagnosis of childhood polyarteritis nodosa (PAN) has become challenging after the definition of deficiency of adenosine deaminase 2 (DADA2).
Sag, Erdal   +10 more
core   +2 more sources

Rituximab Efficacy during a Refractory Polyarteritis Nodosa Flare

open access: yesCase Reports in Medicine, 2009
Polyarteritis nodosa (PAN) is a systemic vasculitis whose severe forms are treated with glucocorticoids and cyclophosphamide. Refractory patients are exposed to many complications, notably accelerated atherosclerosis.
Emmanuel Ribeiro   +7 more
doaj   +2 more sources

Spontaneous kidney rupture in a patient with polyarteritis nodosa

open access: yesJournal of Research in Medical Sciences, 2006
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-sized arteries. It involves the renal arterioles in approximately 80% of cases, but spontaneous retroperitoneal hemorrhage is a rare complication of ...
Ahmad Mohammadi   +2 more
doaj   +1 more source

Polyarteritis nodosa of the spleen

open access: yesJournal of the Belgian Society of Radiology, 2010
Background: A 64-year-old male presented with pain in his right lower leg and progressive swelling of the right ankle, without history of previous trauma. Further anamnesis revealed fever, anorexia and weight loss over the past few weeks.
M Smets   +3 more
doaj   +5 more sources

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