Results 81 to 90 of about 22,409 (253)

Polyarteritis Nodosa – eine verschwindende Erkrankung dank Identifikation der Hauptursache

, 2008
The polyarteritis nodosa is a vasculitis for which the main cause had been identified as hepatitis B, a chronic infectious disease inducing an overshooting immune reaction.
Frey, Felix Julius
core  

Polyarteritis nodosa: decreasing incidence in Poland

Archives of medical science : AMS, 2017
Introduction There are many studies on the epidemiology of the orphan disease polyarteritis nodosa (PAN) in European countries. The use of a hospital morbidity database is an important element of epidemiological analysis.
K. Kanecki, A. Nitsch-Osuch, P. Goryński, W. Wierzba, Patryk Tarka, P. Tyszko   +5 more
semanticscholar   +1 more source

When Fever Defies Diagnosis: Wissler–Fanconi Syndrome as an Atypical Presentation of Adult‐Onset Still's Disease

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Adult‐onset Still's disease should be considered in young adults presenting with fever of unknown origin and inflammatory arthritis, even in the absence of rash or sore throat. Recognition of the Wissler–Fanconi variant and early ferritin testing can prevent diagnostic delay and enable prompt, effective immunosuppressive therapy.
Attaina Najeeb, Kamran Taj, Aqsa Abdul Qader, Salar Sultan, Khadija Waleed, Rahmat Gul Omarzai   +5 more
wiley   +1 more source

Dysautonomia in a cutaneous polyarteritis nodosa patient: evidence of systemic evolving? [PDF]

Beyond Rheumatology
Objective: We report a case of a patient with a cutaneous polyarteritis nodosa who developed dysautonomia and review this association's literature. Case report: A 75-year-old male patient was admitted with a recent history of recurrent ulcers on his ...
J. de Carvalho, T. Larocca Skare, Y. Shoenfeld   +2 more
doaj   +1 more source

Association of autoimmune diseases with biologic agents targeting type 2 immunity: An observational study using a claims database

Rheumatology &Autoimmunity, Volume 6, Issue 1, Page 39-50, March 2026.
This observational study assessed the association between anti‐type 2 biologic agents and the occurrence of autoimmune diseases using a large real‐world claims database. Anti‐IL‐5 and anti‐IgE therapies were associated with an increased occurrence of autoimmune diseases, including rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE ...
Shoichiro Inokuchi
wiley   +1 more source

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, Demolin, G., Delwaide, Jean, Van Severen, M., Demolin, H., Cornet, G.   +5 more
core  

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, Parildar, M, Yunten, N, Oran, I   +3 more
core   +1 more source

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, Gokhan Atis, Ozgur Arikan, Omer Faruk Memis, Hasan Samet Güngör, Turhan Caskurlu   +5 more
core   +1 more source

Bilateral renal subcapsular hematoma caused by polyarteritis nodosa: a case report

CEN Case Reports, 2022
Yui Kambayashi, Ken Iseri, Y. Yamamoto, M. Abe, Y. Wada, R. Yanai, H. Honda   +6 more
semanticscholar   +1 more source

Renal infarction due to polyarteritis nodosa in a patient with angioimmunoblastic T-cell lymphoma: a case report and a brief review of the literature

Diagnostic Pathology, 2012
Angioimmunoblastic T-cell lymphoma is one of the most common subtypes of peripheral T-cell lymphoma (15-20% of all cases), accounting for approximately 1-2% of all non-Hodgkin lymphomas.
Ambrosio Maria, Rocca Bruno, Ginori Alessandro, Onorati Monica, Fabbri Alberto, Carmellini Mario, Lazzi Stefano, Tripodi Sergio   +7 more
doaj   +1 more source