Results 91 to 100 of about 22,409 (253)

Polyarteritis nodosa presenting with hemobilia and intestinal hemorrhage

open access: yes, 1997
Polyarteritis nodosa is a multisystem disease primarily involving the small and medium-sized vessels. Prognosis depends on the presence and severity of visceral involvement.

core   +1 more source

Cutaneous polyarteritis nodosa treated with pentoxifylline and clobetasol propionate: A case report

open access: yesSaudi Journal of Medicine and Medical Sciences, 2018
Cutaneous polyarteritis nodosa (cPAN) is a rare type of cutaneous vasculitis. It affects the small- and medium-sized arteries of the dermis and subcutaneous tissue without extracutaneous involvement.
Nada Abdulaziz A. Alquorain   +2 more
doaj   +1 more source

Seckel syndrome with polyarteritis nodosa

open access: yes, 2004
Seckel syndrome is a rare genetic disorder with a typical "bird-headed" appearance. It could affect many organ systems but renal involvement is uncommon. Polyarteritis nodosa is systemic vasculitic disorder which also involves kidneys.
Kutlu R., Kutlu O., Yakinci C., Alkan A.
core  

Polyarteritis nodosa developing after discoid lupus erythematosus

open access: yes, 2012
  We describe a patient with discoid lupus erythematosus whose pattern of disease evolved into a systemic vasculi - tis polyarteritis nodosa.  
H Longhurst (100361)   +3 more
core   +1 more source

Polyarteritis nodosa

open access: yesActa Médica del Centro, 2012
Polyarteritis nodosa is a rare disease whose incidence is estimated at 4 to 10 cases per million persons, and mainly affects men between 40 and 60 years of age.
Gloria Catalina Bacallao Martínez   +2 more
doaj  

Polyarteritis Nodosa with Bilateral Asynchronous Testicular Necrosis: A Case Report

open access: yesCase Reports in Urology, 2011
Polyarteritis nodosa (PAN) is a systemic vasculitis which may result in thrombosis or aneurysm formation in any organ of the body. We report a case polyarteritis nodosa (PAN) resulting in bilateral asynchronous testicular necrosis.
Nicholas J. Toepfer   +3 more
doaj   +1 more source

Polyarteritis nodosa is an unforeseen borderline paradoxical adverse reaction in a female patient with rheumatoid arthritis treated with tofacitinib

open access: yesСовременная ревматология, 2019
The paper describes the occurrence of polyarteritis nodosa in a patient with rheumatoid arthritis during treatment with tofacitinib. It considers the reasons why this condition should be regarded as an unforeseen borderline paradoxical adverse reaction.
Yu. V. Muraviev   +3 more
doaj   +1 more source

Associations between selected immune-mediated diseases and tuberculosis: record-linkage studies.

open access: yes, 2013
BACKGROUND: Previous studies have suggested that there may be an association between some immune-mediated diseases and risk of tuberculosis (TB). METHODS: We analyzed a database of linked statistical records of hospital admissions and death certificates ...
Michael J Goldacre   +10 more
core   +1 more source

A rare case of polyarteritis nodosa associated with nontuberculous mycobacterial infection

open access: yesClinical Case Reports, 2019
Clinicians should be aware that cutaneous PAN can present with significant extracutaneous and constitutional symptoms which make it hard to differentiate from systemic PAN. The condition can also rarely be associated with NTM infections.
ShengYang Bertrand Lian   +2 more
doaj   +1 more source

A CASE OF FULMINANT POLYARTERITIS NODOSA

open access: yesEurasian Journal of Medicine, 2019
Polyarteritis nodosa (PAN) is a systemic illness characterised by necrotising inflammation of medium-sized arteries leading to aneurysm formation. It affects the viscera and other organs.
Ali Rıza Odabaş   +3 more
doaj  

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