Results 31 to 40 of about 14,024 (212)

Leg muscle involvement in polyarteritis nodosa (limited form)—A rare case report

Radiology Case Reports, 2023
Polyarteritis nodosa is a necrotizing arteritis involving small and medium vessels. Polyarteritis nodosa can have variable presentations depending upon the organ involved.
Rishabh Pratap, MBBS, Gaurav Raj, MD
doaj   +1 more source

Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis

Rheumatology, 2019
Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies.
Izabela Dybowska-Gołota, Magdalena Krajewska-Włodarczyk, Zbigniew Żuber   +2 more
doaj   +1 more source

Cutaneous polyarteritis nodosa causing refractory skin deformation and pigmentation as sequel [PDF]

Anais Brasileiros de Dermatologia, 2017
: A 39-year-old woman presented with prominent and painful livedo reticularis lesions spreading on her upper and lower extremities. Histopathologically, the small-to medium-sized arteries in the deep dermis and subcutis showed necrotizing vasculitis with
Karin Okada, Rina Nakamori, Hitoshi Mizutani, Keiichi Yamanaka   +3 more
doaj   +2 more sources

The challenge of managing patients with polyarteritis nodosa

, 2007
Purpose of review In this short review we focus on the problems faced by clinicians caused by the changing definitions of polyarteritis nodosa. Recent findings the term polyarteritis nodosa has been used for more than 100 years as a diagnostic term for ...
Selga, Daina,, Lund University., Segelmark, Mårten,   +2 more
core   +2 more sources

Familial polyarteritis nodosa [PDF]

Arthritis & Rheumatism, 1994
AbstractFamilial polyarteritis nodosa (PAN) is rare. We describe here two siblings who developed PAN 8 years apart. HLA typing showed that the affected family members shared a common haplotype with their unaffected mother. Further study of the family history suggested the possibility of an inherited disorder of connective tissue predisposing to ...
J C, Mason, M R, Cowie, K A, Davies, J B, Schofield, J, Cambridge, J, Jackson, A, So, S A, Allard, M J, Walport   +8 more
openaire   +2 more sources

Associations between selected immune-mediated diseases and tuberculosis: record-linkage studies. [PDF]

, 2013
BACKGROUND: Previous studies have suggested that there may be an association between some immune-mediated diseases and risk of tuberculosis (TB). METHODS: We analyzed a database of linked statistical records of hospital admissions and death certificates ...
Michael J Goldacre, Goldacre, R, Sreeram V Ramagopalan, Conlon, C, Raph Goldacre, Andrew Skingsley, Ramagopalan, SV, Skingsley, A, Goldacre, MJ, Goldacre, Michael, Chris Conlon   +10 more
core   +2 more sources

Identifying Systemic Lupus Erythematosus From Serum Proteomic Profiles Using Machine Learning and Genetic Risk Stratification

Arthritis &Rheumatology, EarlyView.
Objective Proteome‐wide risk models for lupus remain underexplored. We developed classification models to identify lupus from serum proteomic profiles. Methods Patients with lupus and individuals with other autoimmune diseases in the UK Biobank were included.
Mehmet Hocaoǧlu, Jishnu Das, Amr H. Sawalha   +2 more
wiley   +1 more source

Uma causa rara de perfuração intestinal: poliarterite nodosa. [PDF]

, 1981
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Faria, Márcia Helena Aparecida de
core  

Polyarteritis Nodosa with Cytomegalovirus Enteritis and Jejunoileal Perforation: Report of a Case with a Literature Review

, 2022
Jariya Waisayarat,1 Chayakamon Niyasom,2 Soamarat Vilaiyuk,2 Sani Molagool3 1Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand; 2Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital ...
Niyasom C, Vilaiyuk S, Waisayarat J, Molagool S   +3 more
core  

Effective Performance of the 2022 American College of Rheumatology/EULAR Classification Criteria for Antineutrophil Cytoplasmic Antibody–Associated Vasculitis in Pediatric Patients: An ARChiVe Study

Arthritis &Rheumatology, EarlyView.
Objective To assess the 2022 American College of Rheumatology (ACR)/EULAR classification criteria for antineutrophil cytoplasmic antibody–associated vasculitis (AAV) in children with chronic small‐to‐medium vessel vasculitis. Methods A cohort of 574 patients, identified by physician's diagnosis (MD‐diagnosis) in A Registry of Childhood Vasculitis, was ...
David A. Cabral, Else S. Bosman, Nick McPhate, Simranpreet K. Mann, Kirandeep K. Toor, Kimberly A. Morishita, Raashid Luqmani, Michael W. Beresford, James Bistolarides, Sarah Campillo, Sirirat Charuvanij, Kathryn Cook, Paul Dancey, Marietta de Guzman, Samundeeswari Deepak, Barbara Eberhard, Melissa Elder, Samuel Gagne, Katie Harrison, Adam Huber, Archana Khan, Susan Kim, Marisa S. Klein‐Gitelman, Tzielan C. Lee, Suzanne C. Li, Neil Martin, Flora McErlane, L. Nandini Moorthy, Alvaro H. Orjuela, Jonathan Park, Phil Riley, Alan M. Rosenberg, Susan Shenoi, Vidya Sivaraman, Sodality Sutnga, Tamara Tanner, Stacey E. Tarvin, Marinka Twilt, Linda Wagner‐Weiner, Rae S. M. Yeung, Kelly L. Brown, for the ARChiVe Investigators Network within the PedVas Initiative   +41 more
wiley   +1 more source