نتایج جستجو برای: cutaneous polyarteritis nodosa
تعداد نتایج: 56164 فیلتر نتایج به سال:
PURPOSE To alert ophthalmologists to ocular manifestations that could indicate polyarteritis nodosa. CASE A 71-year-old man exhibited unilateral episcleritis as the primary clinical manifestation of polyarteritis nodosa. OBSERVATIONS The patient's ocular symptoms did not respond well to either topical betamethasone eye drops or low-dose oral prednisone. Five months after the onset of ocular...
Polyarteritis nodosa is a form of vasculitis that affects several organs. Gastrointestinal involvement is frequent, but cases in which the gastrointestinal tract is the only site of disease are rare. In this paper, we report a case of a 40 -yearold patient with polyarteritis nodosa restricted to small part of the small intestine, which underwent resection and anastomosis. Laparotomy was perform...
Background Cutaneous polyarteritis nodosa (c-PAN) is a necrotizing vasculitis of small and medium-sized vessels limited to the skin, characterized by the presence of subcutaneous nodular, painful, non purpuric lesions with or without livedo reticularis occurring predominantly in the lower extremities, with no systemic involvement. The cause of c-PAN is unknown: infectious agents in childhood an...
© 2009 The Authors. doi: 10.2340/00015555-0659 Journal Compilation © 2009 Acta Dermato-Venereologica. ISSN 0001-5555 Sir, Cutaneous polyarteritis nodosa (CPAN) is a necrotizing vasculitis involving smalland medium-sized arteries. It has a benign and chronic course without systemic involvement. Its pathogenesis is thought to involve immunecomplex-mediated reactions (1). We describe here the case...
A 73-year-old man developed refractory multiple hemorrhagic gastric ulcers. Emergent gastrectomy was performed, and the diagnosis of polyarteritis nodosa was made by histologic evaluation of the resected stomach. Although gastric ulceration is a relatively rare complication of polyarteritis nodosa, it should be considered in the differential diagnosis of refractory hemorrhagic gastric ulcers. E...
OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN) E Levy-Lahad, P Elkan-Navon, R Segel, SB Pierce, T Walsh, J Barash, S Padeh, A Zlotogorski, YY Berkun, JJ Press, M Mukamel, PJ Hashkes, LL Harel, M Tekin, F Yalcinkaya, O Kasapcopur, EF Emirogullari, MK Lee, RE Klevit, PF Renbaum, A Weinberg-Shukron, S Zeligson, ...
case presentation a ten-year-old iranian boy was referred to our department with history of recurrent abdominal pain followed by fever, chills, arthralgia and scrotal edema. he suffered from hematuria and gastrointestinal bleeding. his physical exam revealed fever (axillary temperature: 38.7°c), hypertension (150/90 mmhg), hepatomegaly (liver span: 13 cm), orchitis and subcutaneous painful nodu...
Pediatric polyarteritis nodosa is rare systemic necrotizing arteritis involving small- and medium-sized muscular arteries characterized by aneurysmal dilatations involving the vessel wall. Aneurysms associated with polyarteritis nodosa are common in visceral arteries; however intracranial aneurysms have also been reported and can be associated with central nervous system symptoms, significant m...
Cutaneous polyarteritis nodosa (PAN) was first described by Lindberg in 1931. This initial description was followed by many case reports and series, including those of Díaz-Pérez and Winkelmann, who used a strict definition based on cutaneous involvement, and Chen and Daoud who classified the condition into three well differentiated groups. The cutaneous form of PAN is distinct from the systemi...
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