Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.4103/aian.aian_644_24 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Dermatomyositis Masquerading Squamous Cell Carcinoma of the Maxilla (T1F1-γ and Ro-52 Positive): A Case Report and Review of Literature.
Ann Indian Acad Neurol
January 2025
Department of Neurology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Hidden in Plain Sight: Antisynthetase Syndrome Masquerading As Acute Coronary Syndrome and Heart Failure.
Cureus
November 2024
Respiratory Medicine, Dartford and Gravesham National Health Service (NHS) Trust, Dartford, GBR.
Article Synopsis
- * High-resolution CT scans showed ground-glass opacities and indicated a potential overlap of nonspecific interstitial pneumonia and organizing pneumonia, while ruling out pulmonary embolism.
- * Treatment with pulse-dose methylprednisolone and tacrolimus resulted in significant clinical improvement, emphasizing the need for prompt diagnosis and team-based management in conditions like antisynthetase syndrome.
Interferonopathies masquerading as non-Mendelian autoimmune diseases: pattern recognition for early diagnosis.
Front Pediatr
August 2023
Division of Pediatric Rheumatology, Nationwide Children's Hospital, Columbus, OH, United States.
Type I interferonopathies are a broad category of conditions associated with increased type I interferon gene expression and include monogenic autoinflammatory diseases and non-Mendelian autoimmune diseases such as dermatomyositis and systemic lupus erythematosus. While a wide range of clinical presentations among type I interferonopathies exists, these conditions often share several clinical manifestations and implications for treatment. Presenting symptoms may mimic non-Mendelian autoimmune diseases, including vasculitis and systemic lupus erythematosus, leading to delayed or missed diagnosis.
View Article and Find Full Text PDFMuscular Weakness with Calcinosis Cutis_A Case of Juvenile Dermatomyositis in a South Asian Male.
Clin Med Insights Case Rep
June 2023
Mercer School of Medicine, Macon, GA, USA.
Background: Juvenile dermatomyositis (JDM) is an autoimmune connective tissue disorder characterized by an inflammation of proximal muscles of both upper and lower limbs in children below the age of 18 years. The condition mainly involves the proximal muscles and skin but extra-muscular involvement such as the gastrointestinal tract, lungs, and heart are also common.
Case Presentation: We present a case of a 12-year-old south Asian male who developed weakness and muscular pain in all 4 extremities at 3 years of age.
Dermatomyositis Masquerading As Generalized Body Swelling: A Case Report.
Cureus
May 2023
Internal Medicine, All India Institute of Medical Sciences, Rishikesh, IND.
Dermatomyositis (DM) is a systemic autoimmune disease that primarily affects the skin and muscles. The hallmark skin manifestation is a violaceous rash on the face, neck, shoulders, upper chest, and extensor surfaces of the arms and legs, which is often accompanied by edema and can be exacerbated by exposure to sunlight. Generalized limb edema and dysphagia are rare presentations of dermatomyositis.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!