Results 81 to 90 of about 14,024 (212)
Polyarteritis nodosa related to hepatitis B virus infection [PDF]
, 1999 peer reviewedA 66-year-old man was hospitalized for asthenia, weight loss, fever and chills. A polyarteritis nodosa associated with hepatitis B virus infection in a replicative phase was diagnosed.
Belaiche, Jacques +5 more
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Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
, 2014 BackgroundPolyarteritis nodosa is a systemic necrotizing vasculitis with a pathogenesis that is poorly understood. We identified six families with multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive ...
Elkan, PN;Pierce, SB;Segel, R;Walsh, T;Barash, J;Padeh, S;Zlotogorski, A;Berkun, Y;Press, JJ;Mukamel, M;Voth, I;Hashkes, PJ;Harel, L;Hoffer, V;Ling, E;Yalcinkaya, F;Kasapcopur, O;Lee, MK;Klevit, RE;Renbaum, P;Weinberg-Shukron, A;Sener, EF;Schormair, B;Zeligson, S;Marek-Yagel, D;Strom, TM;Shohat, M;Singer, A;Rubinow, A;Pras, E;Winkelmann, J;Tekin, M;Anikster, Y;King, MC;Levy-Lahad, E
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Polyarteritis nodosa presenting with hemobilia and intestinal hemorrhage
, 1997 Polyarteritis nodosa is a multisystem disease primarily involving the small and medium-sized vessels. Prognosis depends on the presence and severity of visceral involvement.
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Multiple intracranial aneurysms in polyarteritis nodosa: MRI and angiography
, 1999 In polyarteritis nodosa involvement of the central nervous system is infrequent; small cerebral infarcts are the most common neuroradiological finding. We report a 10-year-old boy with polyarteritis nodosa and intracranial haemorrhage.
Memis, A +3 more
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A rare case of polyarteritis nodosa associated with nontuberculous mycobacterial infection
Clinical Case Reports, 2019 Clinicians should be aware that cutaneous PAN can present with significant extracutaneous and constitutional symptoms which make it hard to differentiate from systemic PAN. The condition can also rarely be associated with NTM infections.
ShengYang Bertrand Lian +2 more
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A CASE OF FULMINANT POLYARTERITIS NODOSA
Eurasian Journal of Medicine, 2019 Polyarteritis nodosa (PAN) is a systemic illness characterised by necrotising inflammation of medium-sized arteries leading to aneurysm formation. It affects the viscera and other organs.
Ali Rıza Odabaş +3 more
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Polyarteritis nodosa cutanea: a case report
Reumatismo, 2003 Cutaneous vasculitides continue to be difficult to diagnose and treat because of the complexity of these disorders. Current classification schemes are based on clinical findings and histopathologic criteria, so biopsy of an early evolving lesion is the ...
P. Bravi, P. Martini
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Testicular Polyarteritis Nodosa Mimicking Testicular Neoplasm [PDF]
, 2010 Polyarteritis nodosa (PAN) presents mostly as a systemic disease characterized by necrotizing vasculitis affecting small- and medium-sized arteries. Rarely, the inflammatory process is isolated and involves a single organ without systemic manifestations.
Yesim Saglican +5 more
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Supplementary - Tocilizumab for polyarteritis nodosa - Cottu A., et al
Supplementary - Tocilizumab for polyarteritis nodosa - Cottu A., et ...
cottu, adrien
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Cutaneous Polyarteritis Nodosa Presenting Atypically with Severe Pharyngeal Ulceration
Case Reports in Rheumatology, 2019 Polyarteritis nodosa (PAN) is a multisystem, necrotising vasculitis of small- and medium-sized arteries with a predilection for the visceral vessels. Cutaneous PAN is a rare variant with symptomatic vasculitis limited to the skin, typically presenting as
Bayanne Olabi +2 more
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