Results 1 to 10 of about 143 (110)

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   +9 more sources

Cutaneous polyarteritis nodosa: A rare isolated cutaneous vasculitis

open access: yesIndian Dermatology Online Journal, 2012
Cutaneous polyarteritis nodosa (CPAN) is a rare form of cutaneous vasculitis that involves small and medium sized arteries of the dermis and subcutaneous tissue without systemic involvement. It presents with tender subcutaneous nodules, digital gangrene,
Praveen Kumar A Subbanna   +2 more
doaj   +3 more sources

Cutaneous polyarteritis nodosa causing refractory skin deformation and pigmentation as sequel [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2017
: 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   +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

The spectrum of cutaneous polyarteritis nodosa. A case report of two contrasting cases and review of the literature

open access: yesClinical Case Reports, 2022
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   +1 more source

Is macular lymphocytic arteritis limited to the skin? Long-term follow-up of seven patients, [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2020
Background: Macular lymphocytic arteritis most commonly presents as hyperpigmented macules on the lower limbs. The pathogenesis of this disease is still unclear and there is an ongoing debate regarding whether it represents a new form of cutaneous ...
Thâmara Cristiane Alves Batista Morita   +2 more
doaj   +1 more source

Successful use of combined corticosteroids and rituximab in a patient with refractory cutaneous polyarteritis nodosa

open access: yesJournal of Dermatology and Dermatologic Surgery, 2017
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   +1 more
doaj   +1 more source

CUTANEOUS POLYARTERITIS NODOSA: A REPORT OF TWO CASES [PDF]

open access: yesActa Medica Iranica, 1998
Polyarteritis nodosa is a multisystem necrotizing vasculitis of small and medium size muscular arteries in which involvement of the renal and viserat arteries is characteristic.
Z . Nowroozi
doaj   +1 more source

Cutaneous arteritis with compartment syndrome: Case report and review of published works

open access: yesJournal of Cutaneous Immunology and Allergy, 2021
Cutaneous arteritis (CA) is a rare limited form of polyarteritis nodosa (PAN), which usually has a benign prognosis and requires less aggressive therapy.
Satoshi Yoshida   +5 more
doaj   +1 more source

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   +1 more source

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