The spectrum of cutaneous polyarteritis nodosa. A case report of two contrasting cases and review of the literature [PDF]
Cutaneous polyarteritis nodosa is a rare neutrophilic vasculitis. We present two cases that reflect the gamut of this disorder including one case whose delayed diagnosis led to permanent nerve deficit and scarring.
Ian Liang +3 more
doaj +2 more sources
Cutaneous polyarteritis nodosa and concurrent pseudoxanthoma elasticum–like phenotype: A case report [PDF]
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 +2 more sources
Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis [PDF]
Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies.
Izabela Dybowska-Gołota +2 more
doaj +2 more sources
Catastrophic Cutaneous Polyarteritis Nodosa Exacerbated by Emotional Stress [PDF]
Fatima Bawany,1 Gayin Lee,2 Yasmine Nousari,3 Christopher Ritchlin,2 Partik Singh,4 Francisco Tausk2,4 1Department of Dermatology, New York University, New York, NY, USA; 2Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA;
Bawany F +5 more
doaj +2 more sources
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 +2 more sources
Cutaneous Polyarteritis Nodosa Presenting Atypically with Severe Pharyngeal Ulceration [PDF]
Polyarteritis nodosa (PAN) is a multisystem, necrotising vasculitis of small- and medium-sized arteries with a predilection for the visceral vessels. Cutaneous PAN is a rare variant with symptomatic vasculitis limited to the skin, typically presenting as
Bayanne Olabi +2 more
doaj +2 more sources
Cutaneous polyarteritis nodosa treated with pentoxifylline and clobetasol propionate: A case report [PDF]
Cutaneous polyarteritis nodosa (cPAN) is a rare type of cutaneous vasculitis. It affects the small- and medium-sized arteries of the dermis and subcutaneous tissue without extracutaneous involvement.
Nada Abdulaziz A. Alquorain +2 more
doaj +2 more sources
Vasculitis in an Infant Born to a Mother With Longstanding Cutaneous Polyarteritis Nodosa: A Case Report and Review of Literature. [PDF]
ABSTRACT We present a neonate born to a mother with a known diagnosis of cutaneous polyarteritis nodosa (cPAN) who presented with acrocyanosis on the first day of life, which progressed to livedo reticularis and eventual digital necrosis and autoamputation.
Melloy MP, Maguiness S.
europepmc +2 more sources
Cutaneous polyarteritis nodosa causing refractory skin deformation and pigmentation as sequel [PDF]
: A 39-year-old woman presented with prominent and painful livedo reticularis lesions spreading on her upper and lower extremities. Histopathologically, the small-to medium-sized arteries in the deep dermis and subcutis showed necrotizing vasculitis with
Karin Okada +3 more
doaj +3 more sources
Cutaneous polyarteritis nodosa is a rare subtype of polyarteritis nodosa that lacks significant internal organ involvement. It has a relapsing remitting nature and usually is less responsive to conventional treatments.
Ibrahim A Al-Homood
exaly +3 more sources

