Results 31 to 40 of about 22,409 (253)

Sequence-Based Screening of Patients With Idiopathic Polyarteritis Nodosa, Granulomatosis With Polyangiitis, and Microscopic Polyangiitis for Deleterious Genetic Variants in ADA2

Arthritis & Rheumatology, 2020
Deficiency of adenosine deaminase 2 (DADA2) is a monogenic form of vasculitis that can resemble polyarteritis nodosa (PAN). This study was undertaken to identify potential disease‐causing sequence variants in ADA2 in patients with idiopathic PAN ...
O. Schnappauf, Natalia Sampaio Moura, I. Aksentijevich, M. Stoffels, A. Ombrello, P. Hoffmann, K. Barron, E. Remmers, M. Hershfield, S. Kelly, D. Cuthbertson, S. Carette, Sharon A. Chung, Lindsy J. Forbess, N. Khalidi, C. Koening, C. Langford, Carol A. McAlear, P. Monach, L. Moreland, C. Pagnoux, P. Seo, J. Springer, A. Sreih, K. Warrington, S. Ytterberg, D. Kastner, P. Grayson, P. Merkel   +28 more
semanticscholar   +1 more source

Polyarteritis Nodosa

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

Tocilizumab for the treatment of polyarteritis nodosa: a systematic literature review. Correspondence on ‘Tofacitinib for polyarteritis nodosa: a tailored therapy’ by Rimar et al

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, Kiyoshi Shikino, Kosuke Ishizuka, Yosuke Yamauchi, Daiki Yokokawa, Akiko Ikegami, Takanori Uehara, Masatomi Ikusaka   +7 more
doaj   +1 more source

Myocarditis and intramural coronary vasculitis in polyarteritis nodosa: an unusual treatable form of heart failure

ESC Heart Failure, 2020
We describe an uncommon cardiac presentation of polyarteritis nodosa. A 68‐year‐old woman, with a history of fatigue, weight loss, and myalgia of the lower extremities, was admitted for congestive heart failure.
Cristina Chimenti, Maria Alfarano, Federica Toto, Francesca Fanisio, Romina Verardo, Nicola Galea, Luciano Agati, Andrea Frustaci   +7 more
doaj   +1 more source

Polyarteritis nodosa involving the hard palate: A case report [PDF]

, 2013
"Introduction. Polyarteritis nodosa is a rare disease resulting from blood vessel inflammation (vasculitis), causing damage to organ systems and featuring an extended range of possible symptoms. The cause of polyarteritis nodosa is unknown.
MONACO, ANNALISA, Pietropaoli D, Ortu E, MARZO, GIUSEPPE, GIANNONI, Mario, Baldi M   +5 more
core   +1 more source

Familial polyarteritis nodosa [PDF]

Arthritis & Rheumatism, 1994
AbstractFamilial polyarteritis nodosa (PAN) is rare. We describe here two siblings who developed PAN 8 years apart. HLA typing showed that the affected family members shared a common haplotype with their unaffected mother. Further study of the family history suggested the possibility of an inherited disorder of connective tissue predisposing to ...
J C, Mason, M R, Cowie, K A, Davies, J B, Schofield, J, Cambridge, J, Jackson, A, So, S A, Allard, M J, Walport   +8 more
openaire   +2 more sources

Graft Choice and Timing of Coronary Bypass Surgery in Patients with Vasculitis Syndromes: Two Cases Report

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, Rachel Kapelow, Bilge D. Kalyon, Nitzan C. Roth, Arvind Rishi, Maria-Louise Barilla-LaBarca   +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, Hiroshi Asano, Hiroyuki Fukano, Yasuhiro Ohara, Nozomi Shinozuka, Chih-Ping Li, Taketo Yamada   +6 more
doaj   +1 more source