Results 71 to 80 of about 143 (110)
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Myasthenia gravis with cutaneous polyarteritis nodosa

Clinical and Experimental Dermatology, 2006
Cutaneous 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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Cutaneous polyarteritis nodosa: a comprehensive review

International Journal of Dermatology, 2010
AbstractCutaneous 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

Archives of Dermatology, 1977
To 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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Cutaneous polyarteritis nodosa and Crohn's disease

Clinical Rheumatology, 1991
We 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.

VASA. Zeitschrift fur Gefasskrankheiten, 1998
Here we present two characteristic cases of cutaneous polyarteritis nodosa (cutaneous PAN). Cutaneous PAN is characterized by a chronic relapsing benign course over many years. In its mild form it presents with live-do and multiple painful nodular skin lesions mainly of the legs.
D, Kleeman, W, Kempf, G, Burg, J, Hafner
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Benign Cutaneous Polyarteritis Nodosa

Archives of Dermatology, 1991
Benign cutaneous polyarteritis nodosa has been described as having a benign course in contrast to that of systemic classic polyarteritis nodosa. We tested the hypothesis that this histologic distinction is false by reviewing nine consecutive cases with the histologic diagnosis of benign cutaneous polyarteritis nodosa.
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Reappraisal of histopathology of cutaneous polyarteritis nodosa

Journal of Cutaneous Pathology, 2016
BackgroundThere 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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Relapsing polychondritis presenting as cutaneous polyarteritis nodosa

The Clinical Investigator, 1993
Relapsing polychondritis is an infrequently diagnosed, though not necessarily uncommon, systemic disorder characterized by recurrent and potentially destructive inflammation of cartilaginous structures, the eye, and the audiovestibular and cardiovascular systems.
G, Rauh   +3 more
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Cutaneous polyarteritis nodosa

Wadia Journal of Women and Child Health, 2022
Ruturaj Shivajirao Patil   +3 more
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Chronic Cutaneous Polyarteritis Nodosa: A Distinct Subset of Polyarteritis Nodosa?

Archives of Internal Medicine, 1981
To the Editor. —A cutaneous form of polyarteritis nodosa (PN) seems to be a distinct clinical entity, although its distinction has been debated in dermatology journals by a number of writers. 1-6 The patient to be described in this report had chronic PN localized in the right foot.
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