Results 21 to 30 of about 20,949 (222)
Polyarteritis nodosa and deficiency of adenosine deaminase 2– shared genealogy, generations apart
Clinical Immunology, 2020 Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that predominantly affects medium-sized arteries. With the establishment and refinement of vasculitis nomenclature and diagnostic criteria, clinical findings of PAN and distinguishing ...
Zhengping Huang +3 more
semanticscholar +1 more source
CUTANEOUS POLYARTERITIS NODOSA: A REPORT OF TWO CASES [PDF]
Acta Medica Iranica, 1998 Polyarteritis nodosa is a multisystem necrotizing vasculitis of small and medium size muscular arteries in which involvement of the renal and viserat arteries is characteristic.
Z . Nowroozi
doaj +1 more source
Manifestations, clinical course and prognostic markers in cutaneous polyarteritis nodosa
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2020 Cutaneous polyarteritis nodosa (CPAN) is a comparatively rare form of vasculitis that affects small arteries and arterioles in the panniculus and dermo‐subcutaneous junction.
M. Munera‐Campos +5 more
semanticscholar +1 more source
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 +1 more source
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
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 +7 more
doaj +1 more source
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 +7 more
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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 +8 more
openaire +2 more sources
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