Results 31 to 40 of about 143 (110)

An Atypical Case of Vasculitis: When ‘Occult’ 18FDG-PET Scan Findings Create a Classification Dilemma

European Journal of Case Reports in Internal Medicine, 2019
We describe a 66-year old patient with a recurrent ulcer on her right ankle. Biopsy revealed medium-vessel vasculitis consistent with cutaneous polyarteritis nodosa.
Elena Lopez-Francos, Sammy Place, Daphnee Delplace, Frédéric Vandergheynst   +3 more
doaj   +1 more source

Catastrophic Cutaneous Polyarteritis Nodosa Exacerbated by Emotional Stress

Clinical, Cosmetic and Investigational Dermatology, 2022
Fatima Bawany,1 Gayin Lee,2 Yasmine Nousari,3 Christopher Ritchlin,2 Partik Singh,4 Francisco Tausk2,4 1Department of Dermatology, New York University, New York, NY, USA; 2Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA;
Bawany F, Lee G, Nousari Y, Ritchlin C, Singh P, Tausk F   +5 more
doaj  

Inflammatory bowel disease and immune-mediated inflammatory diseases: looking at the less frequent associations

Therapeutic Advances in Gastroenterology, 2022
Patients with inflammatory bowel disease (IBD) often have other immune-mediated inflammatory diseases (IMIDs), and the prevalence of any IMID is higher in IBD patients than in the general population.
Cristina Bezzio, Cristina Della Corte, Marta Vernero, Imma Di Luna, Gianpiero Manes, Simone Saibeni   +5 more
doaj   +1 more source

Poliarterite nodosa cutânea na infância com gangrena digital e possível associação com o estreptococo beta-hemolítico do grupo a: relato de caso e revisão de literatura Cutaneous polyarteritis nodosa in children presenting with digital gangrene and possible association with group a beta hemolytic streptococcus infection

Revista Brasileira de Reumatologia, 2008
A poliarterite nodosa cutânea (PAN cutânea) é uma forma particular de vasculite envolvendo artérias de pequeno e médio calibres. A doença pode ser diferenciada da poliarterite nodosa sistêmica pela sua limitação à pele e ausência de envolvimento visceral.
Karina Silva Marins, Ronaldo Baptista, Vladimir Nentzinsky, Mário Newton Leitão de Azevedo, Blanca Elena Rios Gomes Bica   +4 more
doaj   +1 more source

Misdiagnosed for 14 Years: Adenosine Deaminase 2 (ADA2) Deficiency in a Teen Mimicking Polyarteritis Nodosa

Clinical Case Reports
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disorder caused by loss of function mutations in the ADA2 gene (previously the CECR1 gene) on chromosome 22q11.
Mohammadkian Zarafshani, Masoume Avateffazeli, Seyed Masoud Moeini Taba, Reihaneh Faghihi, Sara Beikmohamadi Hezaveh, Vahid Ziaee, Fatemeh Tahghighi, Maryam Loghman   +7 more
doaj   +1 more source

Classic polyarteritis nodosa presenting initially as a case of cutaneous polyarteritis nodosa: A case report

Asian Journal of Medical Sciences
Classic polyarteritis nodosa (PAN) is an uncommon form of aggressive systemic vasculitis involving small-to-medium sized arteries usually of renal vasculature and other visceral organs but characteristically sparing the lung vasculature. Cutaneous PAN (c-
Sabina Adhikari
doaj   +1 more source

A Unique Case of Systemic Lupus Erythematosus Pelvic Vasculitis

Case Reports in Rheumatology, 2016
The clinical presentation of Systemic Lupus Erythematosus (SLE) is diverse and vasculitis can be a potential manifestation. Cutaneous lesions involving small vessels are the most frequent presentation.
Pamela Traisak, Shristi Basnyat, Hala Eid, Patrick Cronin, Halyna Kuzyshyn, David Feinstein   +5 more
doaj   +1 more source

Poliarterite nodosa due to anti elastase antibody

Microbiologia Medica, 2008
The Authors related one case of polyarteritis nodosa occurred to a men forty eight years old.The clinical was characterized by mesenteric and femoral arteries occlusion and chronic cutaneous ulcers to legs.
Caterina Defendenti, Aldo Cereda, Mariella Saudelli, Maurizio Picca   +3 more
doaj   +1 more source

Classic polyarteritis nodosa in childhood

Indian Journal of Dermatology, 2007
Polyarteritis nodosa (PAN) is a medium-sized vessel vasculitis that usually occurs in 40-60 years of age. It is a rare multisystemic disease that is frequently associated with cutaneous manifestation. It rarely occurs in childhood.
Roy Alok, Nandi Mousomi, Ghosh Sanat, Maiti Arunasis   +3 more
doaj  

Successful treatment of cutaneous polyarteritis nodosa with baricitinib

Journal of Dermatological Treatment
The purpose of the article: Polyarteritis nodosa (PAN) is a rare systemic necrotizing vasculitis preferentially targeting medium-sized arteries. PAN has two clinical entities: systemic PAN (sPAN) and cutaneous PAN (cPAN).
Shihui Zhou, Zhen Zhang, Zhirong Yao, Yifeng Guo   +3 more
doaj   +1 more source