Results 261 to 270 of about 1,552,446 (340)
Flecainide‐Induced Interstitial Lung Disease: A Case Report and Review of the Literature
ABSTRACT This case describes a rare adverse effect in which the subject developed interstitial lung disease after initiating a class IC antiarrhythmic, flecainide. There is no current treatment recommendation for flecainide‐induced interstitial lung disease.
Elizabeth Jenkins +2 more
wiley +1 more source
Graphical abstract illustrating the phenotype‐guided therapeutic approach in severe adult HLH/MAS with SPTCL‐like panniculitis, demonstrating clinical and biochemical response following sequential treatment with therapeutic plasma exchange, intravenous immunoglobulin, and cyclosporine.
Hatem Mousa Taha +2 more
wiley +1 more source
FDG PET‐CT images of giant cell arteritis with mesenteric involvement. ABSTRACT Giant cell arteritis‐associated mesenteric vasculitis is a rare manifestation and often carries significant mortality and morbidity. We present a case of GCA with mesenteric involvement that was at first diagnostically challenging, contributed to by a history of functional ...
Benjamin Rao, Ronan O'Connor
wiley +1 more source
ABSTRACT Sjogren's syndrome (SS) is an autoimmune disorder characterized by inflammation of exocrine glands, often presenting with symptoms such as dry eyes and mouth. Although less common, renal involvement can lead to serious complications like hypokalemic paralysis.
Premendra Vimal +3 more
wiley +1 more source
Coexisting Hepatic and Renal Dysfunction During Pulmonary Tuberculosis Treatment: A Case Report
ABSTRACT Anti‐tuberculosis therapy may rarely cause concurrent liver and kidney injury, with ANCA positivity suggesting immune involvement. This case highlights the importance of early recognition, treatment modification, and multidisciplinary care to prevent complications and ensure effective tuberculosis management.
Irfan Malik +7 more
wiley +1 more source
From Nerves to Vessels: Unmasking Churg‐Strauss Behind Polyneuropathy
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA), formerly Churg‐Strauss vasculitis, is a rare systemic autoimmune disease. Neurological involvement is a significant complication. This report details a case of EGPA with severe, progressive polyneuropathy and atypical serological findings, highlighting diagnostic challenges and the ...
Hiba Antar +2 more
wiley +1 more source
Arthritis &Rheumatology, Volume 78, Issue 5, Page 1032-1037, May 2026.
Ram Raj Singh
wiley +1 more source
Atypical Persistent hyperpigmented cutaneous lesions associated with adult‐onset Still's disease. ABSTRACT We report a case of adult‐onset Still's disease (AOSD) in a 30‐year‐old Ugandan man presenting with migratory polyarthralgia, intermittent fever, lymphadenopathy, and atypical persistent pruritic hyperpigmented plaques.
Abdisalam Ahmed Sandeyl +7 more
wiley +1 more source

