Muscle vasculitis has a distinct clinical and histopathologic profile when compared with IIM, often presenting with distal symptoms and elevated CRP levels.

This story revisits the decades-long enigma of hepatitis—once a silent, misunderstood killer—tracing its medical ...

Unfortunately, I am not familiar with internal specialist in your area and I suggest that you contact your nearest hospital for details. Step into a world where the truth shines bright, and every ...

Relapse is common among patients with systemic polyarteritis nodosa, with mycophenolate performing similarly to cyclophosphamide.

In the next in our series on rare conditions that GPs might only encounter once in a career, Dr James Chambers discusses this rare syndrome and how it should be diagnosed and managed. Eosinophilic ...

They included individuals diagnosed with ANCA-associated vasculitis or polyarteritis nodosa between 1st Jan 2011 and 31st Dec 2020, residing in NR1-NR30. Patients were classified using the European ...

Polyarteritis nodosa is a rare vasculitis in children characterized by necrotizing inflammation in small and medium size arteries. It is classified into systemic and cutaneous PAN according to the ...

According to a new systematic review, skeletal muscle involvement, assessed via MRI, is an early and important clinical feature in PAN and AAV.

ABSTRACT: Polyarteritis nodosa (PAN) affects mostly medium-sized arteries and sometimes small ones as well. The primary methods used to make the diagnosis are through physical examinations, biopsies ...

Read more about AAV treatment As mentioned, the combination of AAV and HIV is exceedingly rare, estimated to be present in less than 1% of individuals with HIV. However, rheumatic disorders are still ...