A case of cutaneous polyarteritis nodosa in autoimmune hepatitis.
نویسندگان
چکیده
© 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 of a patient with autoimmune hepatitis (AIH) who presented with CPAN.
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Polyarteritis nodosa is a rare vasculitis in children characterized by necrotizing inflammation in small and medium size arteries. It is classified into systemic and cutaneous PAN according to the presence of systemic symptoms or visceral involvement. We describe the case of a 14-year-old girl with cutaneous Polyarteritis nodosa with an atypical clinical presentation.
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Cutaneous polyarteritis nodosa (CPN) is an uncommon form of vasculitis. It exists as a separate entity, though bearing similar name with polyarteritis nodosa (PAN) which is an aggressive systemic vasculitis with multi-organ involvement. CPN runs a chronic but benign course. Its aetiology is unknown and it usually presents with painful nodules on the legs with mild constitutional symptoms, and e...
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ورودعنوان ژورنال:
- Acta dermato-venereologica
دوره 89 4 شماره
صفحات -
تاریخ انتشار 2009