Results 21 to 30 of about 2,648 (158)
Cutaneous polyarteritis nodosa: Diagnosis lies skin deep
Indian 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
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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
doaj +1 more source
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: 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
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Cutaneous arteritis: Clinicopathological study of 21 cases
Journal of Cutaneous Immunology and Allergy, 2023 Objectives We conducted this study to clarify the progress of cutaneous arteritis. Methods We examined 21 cases of cutaneous arteritis that were diagnosed at our hospital between 2005 and 2020.
Tomoko Hiraiwa +2 more
doaj +1 more source
Acta Dermato-Venereologica, 2020 Formation of neutrophil extracellular traps has been implicated in autoimmunity. However, the presence and clinical relevance of neutrophil extracellular traps in immune-complex-mediated cutaneous small and medium vessel vasculitides has not been ...
Christina Bergqvist +5 more
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
openaire +3 more sources
Cutaneous polyarteritis nodosa: A rare isolated cutaneous vasculitis
Indian 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 +1 more source