Results 21 to 30 of about 27,510 (305)

Endovascular Biopsy of Vertebrobasilar Aneurysm in Patient With Polyarteritis Nodosa

Frontiers in Neurology, 2021
Background and Purpose: The management of unruptured intracranial aneurysms remains controversial. The decisions to treat are heavily informed by estimated risk of bleeding.
K. Narsinh, K. Narsinh, D. McCoy, Zhengda Sun, Cathra Halabi, K. Meisel, T. Tihan, K. Chaganti, M. Amans, V. Halbach, R. Higashida, S. Hetts, C. Dowd, E. Winkler, A. Abla, T. Nowakowski, D. Cooke   +16 more
semanticscholar   +1 more source

Salmonella infection as a trigger for Polyarteritis Nodosa

European Journal of Case Reports in Internal Medicine, 2020
Polyarteritis nodosa is a systemic necrotizing vasculitis that typically affects medium-sized muscular arteries, with occasional involvement of small muscular arteries. Most cases of polyarteritis nodosa are idiopathic but multiple infectious agents have
Pedro Neves Tavares, Patricia Alves, Rita Lizardo Grácio, Paula Gonçalves Costa, Carla Falcão, Catarina Duarte Santos, Filipa Amado   +6 more
doaj   +1 more source

Cutaneous polyarteritis nodosa and concurrent pseudoxanthoma elasticum–like phenotype: A case report

SAGE Open Medical Case Reports, 2020
We report a unique case of a patient presenting with histologically confirmed pseudoxanthoma elasticum–like phenotype and cutaneous polyarteritis nodosa. Cardiac, gastroenterological, and ophthalmologic evaluations were within normal limits.
Roxana Mititelu, Larry W Cheung, Denis Sasseville   +2 more
doaj   +1 more source

Case report: Polyarteritis nodosa as a substrate for a massive myocardial infarction

Frontiers in Cardiovascular Medicine, 2023
This report describes a rare case of a global myocardial infarction caused by severe vasospasm of the coronary arteries secondary to the administration of pyridostigmine in a patient with polyarteritis nodosa (PAN).
Fabio Solis-Jimenez, Araceli Gonzalez-Ortiz, Juan H. Larios-Lara, Carlos A. Castro-Garcia, Eduardo I. Arteaga-Chan, Fernando Velazquez-Sanchez, Jorge L. Vargas-Estrada, Erika Y. Ramirez-Marcano, Diego Araiza Garaygordobil, Jose L. Briseño De La Cruz, Rodrigo Gopar-Nieto, Daniel Sierra-Lara Martinez, Alexandra Arias-Mendoza   +12 more
doaj   +1 more source

French recommendations for the management of systemic necrotizing vasculitides (polyarteritis nodosa and ANCA-associated vasculitides)

Orphanet Journal of Rare Diseases, 2020
Systemic necrotizing vasculitis comprises a group of diseases resembling polyarteritis nodosa and anti-neutrophil cytoplasmic antibody-associated vasculitis (ANCA): granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis, and ...
B. Terrier, R. Darbon, C. Durel, E. Hachulla, A. Karras, H. Maillard, T. Papo, X. Puéchal, G. Pugnet, T. Quéméneur, M. Samson, C. Taillé, L. Guillevin, Vincent Olivier Karine Patrice Pascal Dominique Olivier La Audard Aumaitre Briot Cacoub Cathebras Chauveau Ch, V. Audard, O. Aumaître, K. Briot, P. Cacoub, P. Cathébras, D. Chauveau, O. Chosidow, L. Chouchana, V. Cottin, D. Cornec, E. Daugas, E. Diot, N. Dupin, K. Karoui, O. Fain, P. Gobert, P. Guilpain, M. Hamidou, A. Hummel, M. Jachiet, S. Jouneau, Noémie Jourde Chiche, C. Landron, C. Le Jeunne, J. Lega, X. Mariette, N. Morel, C. Pagnoux, P. Rémy, F. Vandergheynst   +43 more
semanticscholar   +1 more source

Successful use of combined corticosteroids and rituximab in a patient with refractory cutaneous polyarteritis nodosa

Journal of Dermatology and Dermatologic Surgery, 2017
Cutaneous polyarteritis nodosa is a rare subtype of polyarteritis nodosa that lacks significant internal organ involvement. It has a relapsing remitting nature and usually is less responsive to conventional treatments.
Ibrahim A. Al-Homood, Mohammad A. Aljahlan   +1 more
doaj   +1 more source

Sequence‐Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2

Arthritis & Rheumatology, 2020
Deficiency of adenosine deaminase 2 (DADA2) is a monogenic form of vasculitis that can resemble polyarteritis nodosa (PAN). This study was undertaken to identify potential disease‐causing sequence variants in ADA2 in patients with idiopathic PAN ...
O. Schnappauf, Natalia Sampaio Moura, I. Aksentijevich, M. Stoffels, A. Ombrello, P. Hoffmann, K. Barron, E. Remmers, M. Hershfield, S. Kelly, D. Cuthbertson, S. Carette, Sharon A. Chung, Lindsy J. Forbess, N. Khalidi, C. Koening, C. Langford, Carol A. McAlear, P. Monach, L. Moreland, C. Pagnoux, P. Seo, J. Springer, A. Sreih, K. Warrington, S. Ytterberg, D. Kastner, P. Grayson, P. Merkel   +28 more
semanticscholar   +1 more source

Audio-vestibular symptoms in systemic autoimmune diseases [PDF]

, 2018
Immune-mediated inner ear disease can be primary, when the autoimmune response is against the inner ear, or secondary. The latter is characterized by the involvement of the ear in the presence of systemic autoimmune conditions. Sensorineural hearing loss
Adelchi, Croce, D'AGUANNO, VITTORIO, DE VINCENTIIS, Marco, DE VIRGILIO, ARMANDO, DI STADIO, Arianna, GRECO, Antonio, LONGO, Lucia, RALLI, MASSIMO   +7 more
core   +1 more source

Classic polyarteritis nodosa associated with hepatitis C virus infection: a case report

Journal of Medical Case Reports, 2012
Introduction Hepatitis C virus has been under-recognized as an etiologic factor for polyarteritis nodosa and the presence of hepatitis C antigenemia in patients with polyarteritis nodosa has been reported as insignificant.
Rodrigo Damith, Perera Ruwan, de Silva Janaka   +2 more
doaj   +1 more source

CUTANEOUS POLYARTERITIS NODOSA: A REPORT OF TWO CASES [PDF]

Acta Medica Iranica, 1998
Polyarteritis nodosa is a multisystem necrotizing vasculitis of small and medium size muscular arteries in which involvement of the renal and viserat arteries is characteristic.
Z . Nowroozi
doaj   +1 more source