Results 121 to 130 of about 2,648 (158)
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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
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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Reappraisal of histopathology of cutaneous polyarteritis nodosa
Journal of Cutaneous Pathology, 2016BackgroundThere is controversy on whether lymphocytic thrombophilic arteritis (LTA) and macular arteritis (MA) are a different entity from cutaneous polyarteritis nodosa (C‐PAN).ObjectiveTo evaluate the controversy on LTA/MA by examining the morphologic changes during the dynamic inflammatory process.Materials and methodsA clinical and ...
Ari Morimoto, Ko-Ron Chen
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Myasthenia gravis with cutaneous polyarteritis nodosa
Clinical and Experimental Dermatology, 2006Cutaneous polyarteritis nodosa presents with typical cutaneous lesions of polyarteritis nodosa without visceral involvement at the time of diagnosis. We report a 32-year-old woman with a 12-year history of myasthenia gravis under immunosuppressive treatment, who presented with tender, erythematous nodules 20 mm in diameter on her shins.
F, El Sayed +4 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 FORM OF POLYARTERITIS NODOSA
A.M.A. Archives of Dermatology and Syphilology, 1951KUSSMAUL and Maier 1 in 1866 first described the disease which is now called polyarteritis or periarteritis nodosa. The term of periarteritis is an obvious misnomer, for the essential pathologic picture is that of a panarteritis. The disease is a form of inflammatory, necrotizing and obliterative panarteritis of small arteries, arterioles and ...
W N, SLINGER, V, STARCK
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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: a comprehensive review
International Journal of Dermatology, 2010AbstractCutaneous polyarteritis nodosa is a rare form of vasculitis relating to small‐to‐medium‐sized arteries. Its etiology is unknown. Clinical manifestations include tender subcutaneous nodules, livedo reticularis, cutaneous ulcers and necrosis. Although it is distinct from systemic polyarteritris nodosa in that it lacks significant internal organ ...
Aaron Joseph, Morgan, Robert A, Schwartz
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Cutaneous polyarteritis nodosa and Crohn's disease
Clinical Rheumatology, 1991We report a case of a 57-year-old woman who presented simultaneously cutaneous polyarteritis nodosa and Crohn's disease of the colon. Although similar pathogenic hypotheses have been reported, the association of both diseases is exceptional.
J, Graña Gil +5 more
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Cutaneous Polyarteritis Nodosa
Archives of Dermatology, 1977To the Editor.— Cutaneous polyarteritis nodosa is a benign disease that involves the deeper dermis and subcutis, muscle, and nerves, with only rare cases developing systemic involvement. 1 Remissions occur spontaneously2 or following steroid therapy.
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