Results 1 to 10 of about 16,344 (265)
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 +3 more sources
Techniques in Vascular and Interventional Radiology, 2014 The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a pathologist at the University of Vienna. The initial report describes a 23-year-old man who had a 5-day history of fever and diarrhea. Since then, the definition of PAN has evolved.
Travis Howard +3 more
+5 more sources
Cutaneous polyarteritis nodosa [PDF]
Anais Brasileiros de Dermatologia, 2015 Polyarteritis nodosa is a rare vasculitis in children characterized by necrotizing inflammation in small and medium size arteries. It is classified into systemic and cutaneous PAN according to the presence of systemic symptoms or visceral involvement. We
María Alejandra Matteoda +5 more
doaj +7 more sources
Renal infarction due to polyarteritis nodosa in a patient with angioimmunoblastic T-cell lymphoma: a case report and a brief review of the literature [PDF]
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 +7 more
doaj +4 more sources
Cutaneous polyarteritis nodosa [PDF]
British Journal of Dermatology, 2002 Classic polyarteritis nodosa (PAN) is a segmentary leucocytoclastic vasculitis that affects small- and medium-sized arteries. In 1931, Lindberg (Acta Med Scand 1931; 76: 183-225) described the existence of a cutaneous variant of PAN, without visceral ...
Bauza, A. (Ana) +2 more
core +4 more sources
Case Report: A case of cutaneous polyarteritis nodosa in a child following a streptococcal infection [PDF]
Frontiers in PediatricsBackgroundPolyarteritis nodosa is a rare systemic necrotizing vasculitis that is often overlooked and misdiagnosed in clinical practice. Patients may exhibit fever, rash, myalgia, and further symptoms; in severe instances, this may result in damage to ...
Wei Cheng, Wei Yin, Fan Liu, Wen Yin
doaj +2 more sources
Polyarteritis nodosa presenting with severe upper gastrointestinal bleeding: a case report [PDF]
Journal of Medical Case ReportsBackground Polyarteritis nodosa is a relatively uncommon type of systemic necrotizing vasculitis that primarily affects medium-sized arteries. While gastrointestinal involvement is known in polyarteritis nodosa, heavy gastrointestinal bleeding due to ...
Xin-Yue Xiao +7 more
doaj +2 more sources
Polyarteritis nodosa cutanea: a case report
Reumatismo, 2003 Cutaneous vasculitides continue to be difficult to diagnose and treat because of the complexity of these disorders. Current classification schemes are based on clinical findings and histopathologic criteria, so biopsy of an early evolving lesion is the ...
P. Bravi, P. Martini
doaj +3 more sources
Misdiagnosed for 14 Years: Adenosine Deaminase 2 (ADA2) Deficiency in a Teen Mimicking Polyarteritis Nodosa [PDF]
Clinical Case ReportsThe 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 +7 more
doaj +2 more sources