hemolytic uremic syndrome


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hemolytic

 [he″mo-lit´ik]
pertaining to, characterized by, or producing hemolysis.
hemolytic anemia anemia caused by the increased destruction of erythrocytes. A frequently fatal type occurs in infants as a result of Rh incompatibility with the mother's blood (see Rh factor and erythroblastosis fetalis). Other types result from mismatched blood transfusions; from industrial poisons such as benzene, trinitrotoluene (TNT), or aniline; and from hypersensitivity to certain antibiotics and tranquilizers (drug-induced hemolytic anemia). Another important cause is mechanical obstruction caused by microvascular or valvular abnormalities. In addition, it sometimes occurs as a result of a disorder of the immune response in which B-cell–produced antibodies fail to recognize the body's own erythrocytes and directly attack and destroy them (autoimmune hemolytic anemia). Finally, some types of hemolytic anemia appear in the course of other diseases such as leukemia, hodgkin's disease, other types of cancer, acute alcoholism, and liver diseases. Along with the usual symptoms of anemia, the patient may exhibit jaundice. If the cause of the condition can be determined, and if it can be successfully treated, there is a good chance of recovery. steroids and transfusion therapy are used to treat some types. In other cases, surgical removal of the spleen may bring about great improvement.
hemolytic disease of newborn erythroblastosis fetalis.
hemolytic jaundice a rare, chronic, and generally hereditary disease characterized by periods of excessive hemolysis due to abnormal fragility of the erythrocytes, which are small and spheroidal. It is accompanied by enlargement of the spleen and by jaundice. The hereditary form is also known as familial acholuric jaundice; there is also a rare acquired form. See also hyperbilirubinemia.
hemolytic uremic syndrome a form of thrombotic microangiopathy with renal failure, hemolytic anemia, and severe thrombocytopenia and purpura, usually seen in children but occurring at any age. Some authorities consider it identical to thrombotic thrombocytopenic purpura.

he·mo·lyt·ic u·re·mic syn·drome

[MIM*235400]
hemolytic anemia and thrombocytopenia occurring with acute renal failure; in children, characterized by sudden onset of gastrointestinal bleeding, hematuria, oliguria, and microangiopathic hemolytic anemia; in adults, associated with complications of pregnancy following normal delivery, or associated with oral contraceptive use or with infection; often caused by infection with Escherichia coli.

hemolytic uremic syndrome

a kidney disorder marked by renal failure, microangiopathic hemolytic anemia, and platelet deficiency. The syndrome, the cause of which is unknown, usually occurs in infancy. With conservative management, including dialysis, most infants and children recover. The prognosis in adults is uncertain.

he·mo·lyt·ic u·re·mic syn·drome

(hē'mō-lit'ik yūr-ē'mik sin'drōm)
Combination of hemolytic anemia and thrombocytopenia that occurs with acute renal failure. In children, characterized by sudden onset of gastrointestinal bleeding, hematuria, oliguria, and microangiopathic hemolytic anemia in association with intestinal infection by Shigella, Salmonella, or Escherichia coli strain O157:H7; in adults, associated with complications of pregnancy following normal delivery, with oral contraceptive use, or with infection.
Synonym(s): haemolytic uremic syndrome.
References in periodicals archive ?
Soliris is also approved in the US, the European Union and Canada as the first and only treatment for patients with atypical Hemolytic Uremic Syndrome (aHUS) to inhibit complement-mediated thrombotic microangiopathy, a debilitating, ultra-rare and life-threatening genetic disorder characterized by complement-mediated thrombotic microangiopathy (blood clots in small vessels).
The pathogenesis and treatment of hemolytic uremic syndrome.
Role of plasminogen-activator inhibitor type 1 in the pathogenesis and outcome of the hemolytic uremic syndrome.
The only way to prevent hemolytic uremic syndrome from striking children is to prevent the E.
Atypical Hemolytic Uremic Syndrome is a life-threatening disease characterized by the systemic formation of blood clots (TMAs) throughout the body potentially causing damage to the kidneys and other organs, with complications that may include serious or fatal events including stroke, cardiac issues, and kidney failure.
Current outcomes of TTP and hemolytic uremic syndrome (HUS) have improved dramatically with the use of plasma exchange, which should be initiated promptly at diagnosis.
15, "indicating a lack of association between hemolytic uremic syndrome and antibiotic use (JAMA 288[8]:996-1001, 2002).
Her illness, known as hemolytic uremic syndrome, is a known complication of E.
Doctors now report that three of the infected children died from hemolytic uremic syndrome (HUS) soon after the poisoning.
Nasdaq: ALXN) today announced that researchers will present data from clinical studies of Soliris([R]) (eculizumab) as a treatment for patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), two debilitating, ultra-rare and life-threatening disorders, at the 54th Annual Meeting of the American Society of Hematology (ASH).