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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

Case Report: A case of cutaneous polyarteritis nodosa in a child following a streptococcal infection [PDF]

open access: yesFrontiers in Pediatrics
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]

open access: yesJournal of Medical Case Reports
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

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. 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

Misdiagnosed for 14 Years: Adenosine Deaminase 2 (ADA2) Deficiency in a Teen Mimicking Polyarteritis Nodosa [PDF]

open access: yesClinical Case Reports
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

Polyarteritis Nodosa [PDF]

open access: yesThe Journal of Rheumatology, 2013
Polyarteritis nodosa (PAN) is a systemic illness that most often involves the peripheral nervous system, skin, kidneys, and gastrointestinal tract. In this chapter, we review the diagnostic criteria for PAN, its most common neurological manifestations affecting the peripheral nervous system as well as central nervous system presentations, and discuss ...
Andreas P, Diamantopoulos   +1 more
openaire   +3 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 has evolved.
Howard, Travis   +3 more
openaire   +2 more sources

Cutaneous polyarteritis nodosa and concurrent pseudoxanthoma elasticum–like phenotype: A case report

open access: yesSAGE Open Medical Case Reports, 2020
We report a unique case of a patient presenting with histologically confirmed pseudoxanthoma elasticum–like phenotype and cutaneous polyarteritis nodosa. Cardiac, gastroenterological, and ophthalmologic evaluations were within normal limits.
Roxana Mititelu   +2 more
doaj   +1 more source

Salmonella infection as a trigger for Polyarteritis Nodosa

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2020
Polyarteritis nodosa is a systemic necrotizing vasculitis that typically affects medium-sized muscular arteries, with occasional involvement of small muscular arteries. Most cases of polyarteritis nodosa are idiopathic but multiple infectious agents have
Pedro Neves Tavares   +6 more
doaj   +1 more source

Case report: Polyarteritis nodosa as a substrate for a massive myocardial infarction

open access: yesFrontiers in Cardiovascular Medicine, 2023
This report describes a rare case of a global myocardial infarction caused by severe vasospasm of the coronary arteries secondary to the administration of pyridostigmine in a patient with polyarteritis nodosa (PAN).
Fabio Solis-Jimenez   +12 more
doaj   +1 more source

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