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coronary thrombosis/sembap
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Kawasaki disease associated with hydrops of the gallbladder. A case presentation and review of the literature.
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Mucocutaneous lymph node syndrome is a pediatric illness characterized by fever, conjunctivitis, oropharyngeal lesions, exanthem, peripheral edema, desquamation, and adenopathy. The entity has many possible complications, the most significant of which is coronary artery thrombosis and aneurysm. A
Clinicopathologic analysis of cardiac dysfunction in 52 patients with sickle cell anemia.
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Clinical studies have long suggested the presence of a specific cardiomyopathy in sickle cell anemia secondary to intracoronary thrombosis and subsequent infarction. Fifty-two autopsy patients were studied (48 with SS hemoglobin, 4 with S-C or S-Thal hemoglobin) to ascertain the range of cardiac
Mucocutaneous lymph node syndrome in the United States.
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Sixteen patients with an unusual and distinct symptom complex were encountered during a four-year period. Principal features of this syndrome are (1) fever lasting more than seven days; (2) conjunctival injection; (3) changes in the mouth consisting of erythema of the oropharynx, "strawberry
Simultaneous manifestation of acute myocardial infarction and nephrotic syndrome.
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This report describes the simultaneous manifestation of ischemic heart disease and nephrotic syndrome in a 37-year-old woman presenting with acute anterior myocardial infarction. Symptoms of nephrotic syndrome, such as facial and peripheral edema accompanied by proteinuria and hyperlipidemia, and
Panarteritis precipitating extensive circumferential acute myocardial infarction. A case report.
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It is widely known that other causes than recent coronary thrombosis may precipitate acute myocardial infarction in the presence of coronary atherosclerosis. A 48 year old male patient was admitted due to acute coronary insufficiency. The ECG showed anterolateral necrosis and lateral ischemia.
Preservation of myocardial function with mannitol reperfusate.
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Reperfusion of the globally ischemic myocardium with mannitol has been shown to preserve myocardial function. However, it remains unclear whether the mechanism of mannitol protection relates to its hyperosmolar or free radical scavenging properties. Three groups of isolated, perfused rabbit hearts
Diagnosis and management of Kawasaki disease.
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Kawasaki disease is an acute vasculitis characterized by mucosal inflammation, rash, cervical adenopathy, indurative edema of the hands and feet, and late membranous desquamation of the fingertips. Early cardiac effects include myocarditis (occasionally with congestive heart failure), pericardial
[Kawasaki disease].
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Kawasaki disease (KD), first described in Japan in 1967 by Dr. Tomisaku Kawasaki, is an acute multi system vasculitis of infancy and early childhood characterised by high fever, rash, conjunctivitis, inflammation of the mucous membranes, erythematous induration of the hands and feet and cervical
Thrombin and antithrombotics.
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From injury through healing, thrombin has several important functions in blood clotting, subsequent clot lysis, and tissue repair. These include edema, inflammation, cell recruitment, cellular releases, transformations, mitogenesis, and angiogenesis. Thrombin also participates in disease states,
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