Results 111 to 120 of about 2,648 (158)
Rapidly progressive purpuric plaques in an infant. [PDF]
JAAD Case RepDebruyne J +3 more
europepmc +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
A Bauza, M Idoate
exaly +4 more sources
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Polyarteritis Nodosa and Cutaneous Polyarteritis Nodosa
SKINmed: Dermatology for the Clinician, 2003Cutaneous vasculitis can present with a variety of lesions and associated symptoms. It is important for the clinician to be able to recognize vasculitis lesions and know when to pursue further laboratory studies that will determine the extent of the disease process in a patient.
Courtney R, Herbert, Glenn G, Russo
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Cutaneous Polyarteritis Nodosa
Seminars in Cutaneous Medicine and Surgery, 2007The term polyarteritis nodosa (PAN) presently includes classic systemic PAN, cutaneous PAN, and microscopic PAN (microscopic polyangeiitis). Cutaneous PAN involves the deep dermis and the panniculus, with anatomopathological findings diagnostic for arteritis.
José L, Díaz-Pérez +3 more
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Cutaneous Polyarteritis Nodosa Sine Nodosa
Journal of Cutaneous Medicine and Surgery, 2014Background and Objective: Cutaneous polyarteritis nodosa, a form of vasculitis affecting the small to medium sized arteries, most commonly presents as tender subcutaneous nodules over the lower legs and feet. Other features include livedo reticularis, skin ulcers and tender indurated plaques.
Erica, Merman +4 more
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Cutaneous polyarteritis nodosa in a child.
Pediatric Dermatology, 1998Abstract: Cutaneous polyarteritis nodosa (CPAN) is a benign form of vasculitis of small and medium‐size arteries with a recurrent but benign course without systemic involvement. This entity is very rare in children, with about 45 cases described in the literature we reviewed. Herein we report a 10‐year‐old girl with typical CPAN.
M, Ginarte, M, Pereiro, J, Toribio
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Cutaneous polyarteritis nodosa in children
Journal of the American Academy of Dermatology, 2005The purpose of this study was to present the clinical courses and histologic findings of 4 children with cutaneous vasculitis characterized by tender cutaneous nodules and fever in the absence of major organ involvement. We conducted a retrospective chart review of 4 patients with cutaneous vasculitis followed up for a mean of 68 months (range, 12-114 ...
Basil M, Fathalla +3 more
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Cutaneous polyarteritis nodosa of childhood
Journal of the American Academy of Dermatology, 1994The clinical presentation of childhood polyarteritis nodosa (PAN) can range from isolated cutaneous findings to widespread multisystem involvement. Both the systemic and cutaneous forms are known to occur after streptococcal infection.Our purpose was to emphasize the frequent association of childhood cutaneous PAN with antecedent streptococcal ...
A P, Sheth, J C, Olson, N B, Esterly
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