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Cutaneous polyarteritis nodosa [PDF]
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 +10 more sources
Polyarteritis Nodosa: Old Disease, New Etiologies. [PDF]
Polyarteritis nodosa (PAN), also known as panarteritis nodosa, represents a form of necrotizing vasculitis that predominantly affects medium-sized vessels, although it is not restricted to them and can also involve smaller vessels.
Wolff L+4 more
europepmc +2 more sources
Case Report: A case of cutaneous polyarteritis nodosa in a child following a streptococcal infection [PDF]
BackgroundPolyarteritis nodosa is a rare systemic necrotizing vasculitis that is often overlooked and misdiagnosed in clinical practice. Patients may exhibit fever, rash, myalgia, and further symptoms; in severe instances, this may result in damage to ...
Wei Cheng, Wei Yin, Fan Liu, Wen Yin
doaj +2 more sources
Polyarteritis nodosa presenting with severe upper gastrointestinal bleeding: a case report [PDF]
Background Polyarteritis nodosa is a relatively uncommon type of systemic necrotizing vasculitis that primarily affects medium-sized arteries. While gastrointestinal involvement is known in polyarteritis nodosa, heavy gastrointestinal bleeding due to ...
Xin-Yue Xiao+7 more
doaj +2 more sources
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 +2 more sources
Pericarditis of Polyarteritis Nodosa. [PDF]
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. Its highest incidence is in the fifth-sixth decade of life, with a slight male-to-female predilection.
Ambrogetti R+4 more
europepmc +3 more sources
Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
BACKGROUND Polyarteritis nodosa is a systemic necrotizing vasculitis with a pathogenesis that is poorly understood. We identified six families with multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive ...
Yackov Berkun+2 more
exaly +2 more sources
Polyarteritis nodosa of the spleen
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 +6 more sources
Misdiagnosed for 14 Years: Adenosine Deaminase 2 (ADA2) Deficiency in a Teen Mimicking Polyarteritis Nodosa [PDF]
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disorder caused by loss of function mutations in the ADA2 gene (previously the CECR1 gene) on chromosome 22q11.
Mohammadkian Zarafshani+7 more
doaj +2 more sources
The retinopathy in polyarteritis nodosa. [PDF]
E. Rosen
openalex +5 more sources