Results 191 to 200 of about 50,637 (271)

Life‐Threatening Agranulocytosis Induced by Sinomenine Hydrochloride in Chronic Kidney Disease: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Sinomenine, derived from Sinomenium acutum, is widely used in inflammatory diseases. However, its risk of inducing agranulocytosis is not widely appreciated. We report a life‐threatening case in a 40‐year‐old woman with chronic kidney disease (CKD; baseline estimated glomerular filtration rate [eGFR] as low as 36 mL/min/1.73 m2) who developed ...
Ping Xin, Ruoyan Liu, Yu Zhang, Bin Fu
wiley   +1 more source

Caplan Syndrome: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
Swelling of metacarpophalangeal joints, proximal interphalangeal joints with spindle‐shaped aspects at proximal interphalangeal joints. ABSTRACT Caplan syndrome, known as rheumatoid pneumoconiosis, is a combination of silicosis and rheumatoid arthritis.
Ali Moussa Mahaman Laouali   +12 more
wiley   +1 more source

In Vivo Emergence of Oxacillin Resistance in mecA‐Negative MSSA Endocarditis With Metastatic Infection

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Staphylococcus aureus bacteremia (SAB) is particularly challenging when complicated by infective endocarditis (IE), metastatic spread, or evolving antimicrobial resistance. We describe a 76‐year‐old woman with poorly‐controlled diabetes who presented with bilateral knee septic arthritis and persistent methicillin‐sensitive S.
Leandro Bosch   +5 more
wiley   +1 more source

Diverse diagnostic and management approaches for acute rheumatic fever in Australia and New Zealand: findings of a prospective clinical study. [PDF]

open access: yesBMJ Open
Peiris R   +22 more
europepmc   +1 more source

Severe muscle pain in the absence of enzyme elevation: a clue to the diagnosis of muscular vasculitis

open access: yes
ACR Open Rheumatology, Volume 8, Issue 1, January 2026.
Shay Brikman, Amir Bieber, Guy Dori
wiley   +1 more source

DiGeorge Syndrome Complicated by Secondary Antiphospholipid Syndrome Presenting With Vascular Thrombosis

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT DiGeorge syndrome (22q11.2 deletion syndrome) is a congenital disorder typically identified in infancy, but adult presentations may feature autoimmune and thrombotic complications. We report a 30‐year‐old woman with known DiGeorge syndrome who presented with progressive right lower extremity pain.
Aziz‐ur‐Rahman Khalid   +7 more
wiley   +1 more source

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