Results 151 to 160 of about 20,949 (222)
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Current Opinion in Pediatrics, 2022
Purpose of review The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatment and outcome. Recently deficiency of adenosine deaminase-2 (ADA2), which may present as a polyarteritis nodosa-mimic, is becoming an important part of our practice.
Yelda, Bilginer, Seza, Ozen
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Purpose of review The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatment and outcome. Recently deficiency of adenosine deaminase-2 (ADA2), which may present as a polyarteritis nodosa-mimic, is becoming an important part of our practice.
Yelda, Bilginer, Seza, Ozen
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A case of refractory polyarteritis nodosa successfully treated with rituximab
Modern Rheumatology, 2017Keishi Fujio +2 more
exaly +2 more sources
Systematic review of childhood-onset polyarteritis nodosa and DADA2.
Seminars in Arthritis & Rheumatism, 2021BACKGROUND Diagnosis of childhood polyarteritis nodosa (PAN) has become challenging after the definition of deficiency of adenosine deaminase 2 (DADA2). We aimed to define the differential features of pediatric PAN and DADA2 patients in our center and in
Muserref Kasap Cuceoglu +10 more
semanticscholar +1 more source
Therapeutic options for cutaneous polyarteritis nodosa: a systematic review.
Rheumatology, 2021OBJECTIVE Cutaneous polyarteritis nodosa (CPAN) is a necrotizing vasculitis of the middle-size vessels, confined to the skin. We conducted a systematic review in order to identify studies evaluating the different treatment modalities used in CPAN ...
E. Papachristodoulou +3 more
semanticscholar +1 more source
Rheumatic Disease Clinics of North America, 2015
Abstract Polyarteritis nodosa (PAN) is a necrotizing angiitis, often associated with hepatitis B infection, that predominantly affects medium-sized arteries. Patients usually have systemic features; specific manifestations include peripheral neuropathy, mononeuritis multiplex, skin lesions (subcutaneous nodules, purpura), hypertension,
Lindsy, Forbess, Serguei, Bannykh
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Abstract Polyarteritis nodosa (PAN) is a necrotizing angiitis, often associated with hepatitis B infection, that predominantly affects medium-sized arteries. Patients usually have systemic features; specific manifestations include peripheral neuropathy, mononeuritis multiplex, skin lesions (subcutaneous nodules, purpura), hypertension,
Lindsy, Forbess, Serguei, Bannykh
+5 more sources
Polyarteritis Nodosa and Cutaneous Polyarteritis Nodosa
SKINmed: Dermatology for the Clinician, 2003Cutaneous vasculitis can present with a variety of lesions and associated symptoms. It is important for the clinician to be able to recognize vasculitis lesions and know when to pursue further laboratory studies that will determine the extent of the disease process in a patient.
Courtney R, Herbert, Glenn G, Russo
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Comprehensive Therapy, 2007
Polyarteritis nodosa, as a diagnosis, has been progressively narrowed from a collection of ill-defined vasculitides to its current definition as a systemic transmural necrotizing vasculitis that usually affects medium-sized muscular arteries and sometimes small muscular arteries, commonly within the kidneys, gastrointestinal tract, skin, nerves, joints,
H David, Pettigrew +2 more
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Polyarteritis nodosa, as a diagnosis, has been progressively narrowed from a collection of ill-defined vasculitides to its current definition as a systemic transmural necrotizing vasculitis that usually affects medium-sized muscular arteries and sometimes small muscular arteries, commonly within the kidneys, gastrointestinal tract, skin, nerves, joints,
H David, Pettigrew +2 more
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2016
Polyarteritis nodosa (PAN) is a rare vasculitis affecting middle-sized arteries. Its annual incidence in Europe is estimated to range between 0 and 1.6 cases per million, while the prevalence is about 31 cases per million. The frequency of hepatitis B virus (HBV)-related PAN has declined in developed countries since vaccination against HBV has been ...
Pipitone N., Salvarani C.
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Polyarteritis nodosa (PAN) is a rare vasculitis affecting middle-sized arteries. Its annual incidence in Europe is estimated to range between 0 and 1.6 cases per million, while the prevalence is about 31 cases per million. The frequency of hepatitis B virus (HBV)-related PAN has declined in developed countries since vaccination against HBV has been ...
Pipitone N., Salvarani C.
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Polyarteritis nodosa isolated to muscles-A case series with a review of the literature.
Seminars in Arthritis & Rheumatism, 2019Muscular polyarteritis nodosa where disease is isolated to skeletal muscle is a rare and often poorly recognised clinical entity. Patients typically present with fever and severe muscle pain limiting ability to ambulate without rise in creatine kinase ...
Luckshman Ganeshanandan +3 more
semanticscholar +1 more source
Polyarteritis nodosa of epididymis
Urology, 1983Abstract A young man with a scrotal swelling on his left side was found to have an acute necrotizing vasculitis involving epididymal arteries and veins. No systemic symptoms were present.
N R, McLean, R A, Burnett
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