Results 71 to 80 of about 27,299 (305)
대한영상의학회지, 2017 Multiple intrahepatic arterial aneurysms and spontaneous aneurysmal rupture associated with polyarteritis nodosa leading to hemoperitoneum are extremely rare occurrences, but the conditions can be life-threatening if left untreated because of the risk of
Myung Jin Seol +3 more
doaj +1 more source
Uma causa rara de perfuração intestinal: poliarterite nodosa. [PDF]
, 1981 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Faria, Márcia Helena Aparecida de
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Clonal hematopoiesis of indeterminate potential and the risk of autoimmune diseases
Journal of Internal Medicine, Volume 297, Issue 6, Page 642-656, June 2025.Abstract Background Clonal hematopoiesis of indeterminate potential (CHIP), characterized by the age‐related expansion of blood cells carrying preleukemic mutations, is associated with immune aging. This study aimed to investigate the association between CHIP and established autoimmune diseases. Methods We analyzed baseline data from 456,692 UK Biobank
Hanzhang Wu +4 more
wiley +1 more source
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
A case of polyarteritis nodosa limited to the right calf muscles, fascia, and skin: a case report [PDF]
, 2011 Introduction Limited polyarteritis nodosa is a rare benign disease that usually responds well to systemic corticosteroid treatment. We report a case limited to calf muscles, fascia, and skin treated with local corticosteroid therapy directed to the ...
A Balbir-Gurman +16 more
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Fulminant Wegener's granulomatosis: A case report [PDF]
, 2013 Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž. +3 more
core +1 more source
Association between hypertensive disorders of pregnancy and placenta accreta spectrum
Pregnancy, Volume 1, Issue 3, May 2025.Abstract Introduction Placenta accreta spectrum and hypertensive disorders of pregnancy are two significant contributors to severe maternal morbidity and fetal prematurity that may have related but opposite uteroplacental vascular origins. However, the relationship between these conditions is uncertain.
Matthew Givens +6 more
wiley +1 more source
Clinical and Experimental Neuroimmunology, Volume 16, Issue 2, Page 98-107, May 2025.Abstract Objectives Reports of real‐world data concerning chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) are limited in Japan. This study aimed to investigate the diagnostic testing and treatment performed in patients diagnosed with CIDP in Japan. Methods Using a Japanese commercial medical information database, we analyzed diagnostic
Motoi Kuwahara +5 more
wiley +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
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