Results 51 to 60 of about 20,949 (222)
Clinical Case Reports, 2022 Cutaneous polyarteritis nodosa is a rare neutrophilic vasculitis. We present two cases that reflect the gamut of this disorder including one case whose delayed diagnosis led to permanent nerve deficit and scarring.
Ian Liang +3 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Takayasu arteritis (TA) is a rare chronic granulomatous large‐vessel vasculitis predominantly affecting the aorta and its major branches, leading to stenosis, occlusion, or aneurysm formation. It typically presents in young women, though atypical cases can occur in older adults.
Chao Liu +6 more
wiley +1 more source
Metabolic myopathy presenting with polyarteritis nodosa: a case report
Journal of Medical Case Reports, 2011 Introduction To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa.
Elbalkhi Amro +3 more
doaj +1 more source
Treatment of polyarteritis nodosa with tocilizumab: a new therapeutic approach?
RMD Open, 2017 We describe the effect of interleukin 6 (IL-6) blockade using tocilizumab (TCZ) for inducing and maintaining remission of refractory polyarteritis nodosa (PAN).
A. Saunier +5 more
semanticscholar +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT The coexistence of primary phospholipase A2 receptor positive membranous nephropathy and AA amyloidosis in a patient with chronic hepatitis B is an exceedingly rare triad presenting a profound diagnostic and therapeutic challenge. A 38‐year‐old Ethiopian man with nephrotic syndrome and chronic hepatitis B had dual pathology on renal biopsy ...
Betelhem Abreham +4 more
wiley +1 more source
Chronic polyarthritis as the first manifestation of childhood systemic polyarteritis nodosa
Einstein (São Paulo)Arthritis has been reported as an acute pattern, generally evanescent with oligoarthritis, mostly affecting knees and ankles in childhood systemic polyarteritis nodosa.
Glaucia Vanessa Novak +5 more
doaj +1 more source
Cutaneous polyarteritis nodosa: A case report with a brief review of literature
Medical Journal of Dr. D.Y. Patil University, 2013 Polyarteritis nodosa (PAN) is a rare vasculitis with multisystem involvement. The definition, diagnostic criteria and validity of cutaneous polyarteritis nodosa (c-PAN) as a variant of classic PAN limited to skin have continued to remain disputed.
Yugal K Sharma +3 more
doaj +1 more source
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.Objective Gain‐of‐function variants in IDH1 and IDH2 are enriched among individuals with coexisting myeloid neoplasms and autoimmune diseases. However, the association between IDH1/IDH2 variants and rheumatic diseases independent of hematologic neoplasms remains unclear. We investigated the association between rare gain‐of‐function and loss‐of‐function
Mahmut S. Kaymakci +3 more
wiley +1 more source
Spontaneous kidney rupture in a patient with polyarteritis nodosa
Journal of Research in Medical Sciences, 2006 Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-sized arteries. It involves the renal arterioles in approximately 80% of cases, but spontaneous retroperitoneal hemorrhage is a rare complication of ...
Ahmad Mohammadi +2 more
doaj
ACR Open Rheumatology, Volume 8, Issue 4, April 2026.Objective Medium‐vessel vasculitis involving the visceral vasculature in adults is rare. Pancreatic ductal adenocarcinoma (PDAC) has been implicated in medium artery vascular thickening secondary to extravascular migratory metastasis with involvement of the celiac and superior mesenteric vessels.
Maryam Own +2 more
wiley +1 more source