Results 11 to 20 of about 10,688 (221)

Vasculitis in an Infant Born to a Mother With Longstanding Cutaneous Polyarteritis Nodosa: A Case Report and Review of Literature. [PDF]

Pediatr Dermatol
ABSTRACT We present a neonate born to a mother with a known diagnosis of cutaneous polyarteritis nodosa (cPAN) who presented with acrocyanosis on the first day of life, which progressed to livedo reticularis and eventual digital necrosis and autoamputation.
Melloy MP, Maguiness S.
europepmc   +2 more sources

Successful use of combined corticosteroids and rituximab in a patient with refractory cutaneous polyarteritis nodosa

Journal of Dermatology and Dermatologic Surgery, 2017
Cutaneous polyarteritis nodosa is a rare subtype of polyarteritis nodosa that lacks significant internal organ involvement. It has a relapsing remitting nature and usually is less responsive to conventional treatments.
Ibrahim A. Al-Homood, Mohammad A. Aljahlan   +1 more
doaj   +1 more source

Classic polyarteritis nodosa associated with hepatitis C virus infection: a case report

Journal of Medical Case Reports, 2012
Introduction Hepatitis C virus has been under-recognized as an etiologic factor for polyarteritis nodosa and the presence of hepatitis C antigenemia in patients with polyarteritis nodosa has been reported as insignificant.
Rodrigo Damith, Perera Ruwan, de Silva Janaka   +2 more
doaj   +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

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

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

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

A Case of Polyarteritis Nodosa Associated with Vertebral Artery Vasculitis Treated Successfully with Tocilizumab and Cyclophosphamide

Case Reports in Pediatrics, 2016
Pediatric polyarteritis nodosa is rare systemic necrotizing arteritis involving small- and medium-sized muscular arteries characterized by aneurysmal dilatations involving the vessel wall.
Kae Watanabe, Dhanashree A. Rajderkar, Renee F. Modica   +2 more
doaj   +1 more source

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