Results 31 to 40 of about 27,510 (305)
Turkish Journal of Internal Medicine, 2021 Aortic diseases have high mortality and are usually late or misdiagnosed. Especially in patients with inflammatory vasculitis, diagnosis is often confused with other causes of chest pain and this causes a delay in diagnosis.
Hatice Taşkan +4 more
doaj +1 more source
Uveitis, 2020 The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a Pathologist at the University of Vienna.(1) The initial report describes a 23 year-old man who had a five-day history of fever and diarrhea.
Jordan A. Ueberroth
semanticscholar +1 more source
Systemic lupus erythematosus and hearing disorders: literature review and meta-analysis of clinical and temporal bone findings [PDF]
, 2017 Objective: This literature review and meta-analysis was performed to evaluate the correlations among hearing and vestibular clinical symptoms, temporal bone findings, and pathological mechanisms in patients with systemic lupus erythematosus (SLE).
DI STADIO, Arianna, Ralli, Massimo
core +1 more source
Annals of the Rheumatic Diseases, 2020 We read the paper by Rimar et al 1 in your journal with great interest. They reported the case with refractory polyarteritis nodosa treated with tofacitinib, a janus kinase inhibitor, successfully.
M. Akiyama, Y. Kaneko, T. Takeuchi
semanticscholar +1 more source
Muscular Polyarteritis Nodosa: A Case Series Study of 6 Patients
Annals of Internal Medicine: Clinical Cases, 2022 A subset of polyarteritis nodosa known as muscular polyarteritis nodosa (MPAN) is a disease process that remains mostly limited to the muscle. Here, we report 6 patient cases of MPAN for which we investigated the clinical features. We examined 6 patients
Fumitoshi Fukuzawa +7 more
doaj +1 more source
Arterial distensibility in children and teenagers: Normal evolution and the effect of childhood vasculitis [PDF]
, 2002 Background: Polyarteritis nodosa is a necrotising vasculitis of the medium sized and small muscular arteries. The inflammatory and subsequent reparative processes may alter the arterial mechanical properties.
Brogan, PA +4 more
core +2 more sources
Medicine Science, 2014 Polyarteritis nodosa is multisystem disease with necrotizing vasculitis of middle and small sized arteries. Takayasu arteritis is a rare nonspecific inflammatory disease with unknown cause, predominantly affecting the aorta and its main branches.
Onur Gurer, Ismail Haberal
doaj +1 more source
A rare case of Polyarteritis Nodosa associated with autoimmune hepatitis: a case report
BMC Rheumatology, 2021 Background Polyarteritis nodosa is a type of vasculitis affecting medium- and small-sized arteries that has been associated with hepatitis B but does not have an established relationship with autoimmune hepatitis.
Freda Kennedy +5 more
doaj +1 more source
Necrosis of the small intestine leading to a diagnosis of polyarteritis nodosa: a case report
Journal of Medical Case Reports, 2019 Background Polyarteritis nodosa is a disease that presents with necrotizing vasculitis in small and medium-sized arteries. It may occur in various organs, but approximately half of cases have gastrointestinal involvement.
Saori Yajima +6 more
doaj +1 more source
Spontaneous kidney rupture in polyarteritis nodosa presenting as an acute abdomen [PDF]
, 1991 CITATION: Edelstein, C. L. & Welke, H. 1991. Spontaneous kidney rupture in polyarteritis nodosa presenting as an acute abdome. South African Medical Journal, 79:52-53.The original publication is available at http://www.samj.org.zaAn acute abdomen in a ...
Edelstein, C. L., Welke, H.
core +1 more source