Results 61 to 70 of about 143 (110)
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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
2021Cutaneous involvement of medium vessel vasculitis most commonly presents with features of inflammatory subcutaneous nodules, purpura, livedo reticularis, and ulceration. The clinical and histopathologic features of isolated cutaneous polyarteritis nodosa (c-PAN) are indistinguishable from the cutaneous involvement of systemic polyarteritis nodosa ...
Matthew J. Koster +1 more
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CUTANEOUS POLYARTERITIS NODOSA
British Journal of Dermatology, 1972Summary.— The case histories of 102 consecutive patients suffering from polyarteritis nodosa were reviewed. The 17 patients with skin lesions were personally examined and investigated. Thirteen were found to have polyarteritis affecting the skin. In one of these cutaneous involvement occurred only 4 days before death and 5 weeks after the onset of the ...
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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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Minocycline-Induced Cutaneous Polyarteritis Nodosa
JCR: Journal of Clinical Rheumatology, 2007Minocycline is a tetracycline derivative with multiple clinical uses including the treatment of various infections, acne vulgaris, and rosacea. Numerous adverse events have been reported ranging from minor complaints such as nausea, to serious life-threatening toxicities such as acute renal failure, hepatotoxicity, and systemic lupus erythematosus.
Rodney, Tehrani +4 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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Cutaneous Polyarteritis Nodosa
Archives of Dermatology, 1983† A patient had cutaneous polyarteritis nodosa associated with Crohn's disease. Immunopathologic studies disclosed evidence of circulating immune complexes as measured by C1q binding. Immunofluorescent microscopy of lesional skin showed C3 and fibrin deposition.
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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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