Dermatomyositis diagnostic criteria In order for your doctor to make an official dermatomyositis diagnosis, you have to meet certain criteria. Except for amyopathic dermatomyositis, which is ...

Patients with idiopathic inflammatory myopathies, particularly polymyositis, show a high prevalence of atherosclerotic cardiovascular disease.

AI has shown promise by analysing data from patient records to recognise complex patterns within large datasets, which can aid in the ...

Systemic Symptoms: In addition to skin and muscle involvement, dermatomyositis can also affect other organs and systems in the body, leading to symptoms such as fever, weight loss, and fatigue.

classic dermatomyositis rash, or biopsy indicating amyopathic disease were eligible for inclusion. Each patient underwent at least 1 CA-125 or PET/CT cancer screening test within 5 years of IIM ...

Meanwhile, an uncle has ptosis but no diagnosis yet, and a daughter has dermatomyositis. Like MG, dermatomyositis is an autoimmune disease that causes muscle weakness. The patient, who’s CTLA4 ...

Expansion of Phase 1 CALiPSO-1 trial of CNTY-101 in autoimmune disease to include diffuse cutaneous systemic sclerosis and idiopathic ...

Furthermore, patients with radiographic patterns of NSIP+OP or diffuse alveolar damage (DAD) had more risk factors for poor prognosis, with 12-month mortality rates of 45.9% and 100%, respectively.

A diagnosis of anti-MDA5 amyopathic dermatomyositis was made. Treatment with a combination of oral prednisolone (30 mg per day for 2 weeks, tapered over 2 months), mycophenolate mofetil (2 g per day), ...

The revised diagnosis was dermatomyositis. The patient was admitted to hospital for observation and the dose of oral prednisolone increased to 60 mg/day. Azathioprine was started at 50 mg/day. On the ...