Results 31 to 40 of about 4,605 (161)
Acute cholestasis as uncommon onset of Kawasaki disease: a case report
Background Kawasaki disease (KD) or mucocutaneous lymph node syndrome is a vasculitis that mostly occurs in young children. Adult-onset KD (AKD) is rare and often misdiagnosed. Here we report a rare case of KD with cholestasis as principal symptom.
Massimo Gallerani +3 more
doaj +1 more source
Differentiation between incomplete Kawasaki disease and secondary hemophagocytic lymphohistiocytosis following Kawasaki disease using N-terminal pro-brain natriuretic peptide [PDF]
PurposeHemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome with many causes, including Kawasaki disease (KD). The purpose of this study was to identify the laboratory tests needed to easily differentiate KD with HLH from incomplete ...
Jung Eun Choi +6 more
doaj +1 more source
Kawasaki disease (KD) is a systemic vasculitis affecting children younger than 5 years of age. Early period in life is marked by rapid somatic growth with cell proliferation and immaturity of the immunity with dominant innate immune system.
Jin-Hee Oh, Soyun Cho, Jin A Choi
doaj +1 more source
Tuberculosis Presenting as Migratory Arthritis: A Case Report from Iraq
ABSTRACT Extrapulmonary tuberculosis is uncommon, and musculoskeletal involvement presenting as migratory arthritis is particularly rare in immunocompetent individuals, often leading to misdiagnosis and delayed treatment. We report the case of a 66‐year‐old man with diabetes mellitus who presented with recurrent migratory inflammatory arthritis ...
Farah Jaafar Mahdi +7 more
wiley +1 more source
Giant coronary artery aneurysms in a 58-year-old
All giant Kawasaki aneurysms may not regress fully; some may eventually calcify, undergo thrombosis, and get detected in asymptomatic adults at later age.
Anil Kumar Singhi +2 more
doaj +1 more source
Kawasaki Shock Syndrome with Initial Presentation as Neck lymphadenitis: A Case Report
Kawasaki disease (KD) is an acute systemic vasculitis of unknown cause that mainly affects infants and children and can result in coronary artery complications if left untreated.
Yi-Ting Cheng +5 more
doaj +1 more source
Kawasaki Disease Accompanied by Acute Generalized Exanthematous Pustulosis
ABSTRACT Acute generalized exanthematous pustulosis (AGEP) is a rare but serious adverse skin reaction usually caused by drugs. We reported a 4‐year‐old boy diagnosed with Kawasaki disease (KD) accompanied by AGEP who presented with typical symptoms of KD, including fever, scarlet‐like rash, swollen extremities, cervical lymph node swelling ...
Wen Li +4 more
wiley +1 more source
Cardiovascular risk factors of early atherosclerosis in school-aged children after Kawasaki disease [PDF]
PurposeThe aim of this study was to determine whether school-aged children with Kawasaki disease (KD) have an increased risk for early atherosclerosis.MethodsThe study included 98 children.
Hyun Jeong Cho +4 more
doaj +1 more source
Abstract Background Penile sexual sensation relies on intricate neural structures that remain incompletely characterized. Immunohistological insights into their development and organization can enhance understanding of penile neuroanatomy and function, while optimizing surgical outcomes.
Alfonso Cepeda‐Emiliani +6 more
wiley +1 more source
ABSTRACT Background Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive cancers, typically diagnosed at an advanced stage due to its subtle and often absent early symptoms. Despite representing only 3% of new cancer cases, it is projected to become the second leading cause of cancer‐related deaths by 2030.
Muhammad Masroor Hussain +5 more
wiley +1 more source

