Results 11 to 20 of about 143 (110)
Peripheral limb gangrene in a child with polyarteritis nodosa: An unusual presentation
Indian Journal of Rheumatology, 2022 Polyarteritis nodosa (PAN) is a necrotizing vasculitis predominantly affecting medium-sized muscular arteries. PAN is comparatively rarer in childhood.
Namrata Patil +5 more
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Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
Rheumatology, 2019 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 +1 more source
Cutaneous polyarteritis nodosa
British Journal of Dermatology, 2002 Classic polyarteritis nodosa (PAN) is a segmentary leucocytoclastic vasculitis that affects small- and medium-sized arteries. In 1931, Lindberg (Acta Med Scand 1931; 76: 183-225) described the existence of a cutaneous variant of PAN, without visceral involvement and with a more favourable prognosis. We present four patients diagnosed with cutaneous PAN
España, A. (Agustín) +2 more
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Dysautonomia in a cutaneous polyarteritis nodosa patient: evidence of systemic evolving? [PDF]
Beyond RheumatologyObjective: We report a case of a patient with a cutaneous polyarteritis nodosa who developed dysautonomia and review this association's literature. Case report: A 75-year-old male patient was admitted with a recent history of recurrent ulcers on his ...
J. de Carvalho +2 more
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Polyarteritis nodosa cutanea: a case report
Reumatismo, 2003 Cutaneous vasculitides continue to be difficult to diagnose and treat because of the complexity of these disorders. Current classification schemes are based on clinical findings and histopathologic criteria, so biopsy of an early evolving lesion is the ...
P. Bravi, P. Martini
doaj +1 more source
Journal of Clinical Rheumatology and Immunology, 2023 Polyarteritis nodosa (PAN) is a medium-sized vessel vasculitis often presenting report as both stenotic and aneurysmal lesions. Association with antiphospholipid antibody (aPL) has also been described.
Cheryl Chun Man Ng
doaj +1 more source
Cutaneous polyarteritis nodosa
Wiadomosci lekarskie (Warsaw, Poland : 1960), 2018 Cutaneous polyarteritis nodosa is a rare disease that affects vessels of the deep skin and the subcutaneous tissue. Its etiopathology remains unknown. It predominantly affects skin, and the main cutaneous symptoms are subcutaneous nodules, livedo reticularis, and ulcerations that are mainly located on legs. Cutaneous polyarteritis nodosa can also cause
Cindy E. Owen, Jeffrey P. Callen
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Cutaneous polyarteritis nodosa treated with pentoxifylline and clobetasol propionate: A case report
Saudi Journal of Medicine and Medical Sciences, 2018 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 +1 more source
Cutaneous polyarteritis nodosa: A case report with a brief review of literature
Medical Journal of Dr. D.Y. Patil University, 2013 Polyarteritis nodosa (PAN) is a rare vasculitis with multisystem involvement. The definition, diagnostic criteria and validity of cutaneous polyarteritis nodosa (c-PAN) as a variant of classic PAN limited to skin have continued to remain disputed.
Yugal K Sharma +3 more
doaj +1 more source
Cutaneous Polyarteritis Nodosa Presenting Atypically with Severe Pharyngeal Ulceration
Case Reports in Rheumatology, 2019 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 +1 more source