Results 191 to 200 of about 375,685 (295)

Possible Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections (PANDAS) Presenting in Late Adolescence and Early Adulthood: A Case Series

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT PANDAS‐like syndromes may rarely occur beyond childhood. Although these patients may meet criteria for PANS, recognizing a possible streptococcal‐triggered subgroup remains important for diagnosis, future biomarker discovery, and refinement of disease classification.
Tariq A. Madani   +3 more
wiley   +1 more source

Clinical characteristics and predictors of adverse outcomes in children with acute rheumatic fever from a high-endemic region of Brazil. [PDF]

open access: yesFront Cardiovasc Med
Mendoza RF   +10 more
europepmc   +1 more source

Unexplained Optic Neuritis and New Heart Block: A Diagnostically Challenging Case of Probable Sarcoidosis

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Sarcoidosis is a systemic inflammatory disease of unknown etiology and manifests in multiple forms. It can affect several organs within the body; however, the lungs and intra‐thoracic lymph nodes are involved in the majority of cases. Diagnosis can be challenging due to the diversity of presentation and similarities to other systemic diseases.
Chetan Kamath   +4 more
wiley   +1 more source

Rapidly Progressing Interstitial Fibrosis and Glomerulonephritis due to Granulomatosis With Polyangiitis Presenting With Calf Pain

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT We describe a 51‐year‐old male presenting with bilateral calf pain and found to have rapidly progressing pulmonary‐renal syndrome due to GPA vasculitis, despite completing an empiric course of steroids for a gout flare. This case underscores the heterogeneous nature of GPA and the importance of early strong immunosuppressive therapy.
Lily Gupta (Allison)   +2 more
wiley   +1 more source

Diagnostic Pitfall: Mixed Connective Tissue Disease‐Associated Pulmonary Hypertension Presenting With Postpartum Right‐Sided Heart Failure in a 21‐Year‐Old—Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Mixed connective tissue disease is a multisystem autoimmune condition characterized by overlapping clinical and serological features related to anti‐U1‐RNP antibodies of at least two connective tissue diseases. It may present with myocarditis, pericarditis, pulmonary arterial hypertension, and, less commonly, heart failure.
Sai Santhosha Mrudula Alla   +10 more
wiley   +1 more source

Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis in a Child With Coronary Artery Dilation and SARS‐CoV‐2 Positivity: Diagnostic Overlap With MIS‐C. A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT Macrophage activation syndrome (MAS) can complicate systemic juvenile idiopathic arthritis (sJIA) evolving over weeks. With SARS‐CoV‐2 positivity and coronary dilation, MIS‐C cannot be excluded, and here the timeline and serology do not establish SARS‐CoV‐2 as the trigger.
Ayham Slimi   +3 more
wiley   +1 more source

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