Download Citation on ResearchGate | Esferocitosis hereditaria: Aspectos clínicos , La prueba más utilizada para el diagnóstico de la EH es la fragilidad. Protocolo diagnóstico de las anemias hemolíticas Crisis aplásica por Parvovirus B19 y virus de Epstein-Barr en paciente con esferocitosis hereditaria. Article. Esferocitosis hereditaria: Revisión. Parte I. Historia, demografía, etiopatogenia y diagnóstico Translated title: Hereditary spherocytosis: Review. Part I. History.
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Abstract Hematological automates using double beam laser diffraction by artificially spherized red blood cells determine both volume and hemoglobin concentration of a very large number of cells, even indicating percentages of aberrant elements.
A firewall is blocking access herediraria Prezi content. The high association of HS with both diabetes and iron overload suggest damage of the endocrine pancreas by the latter, as it is also seen in genetic hemochromatosis. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting diagnosstico diagnosis of HS are in reality rare.
This explains the discrepancy between these values.
La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized by anemia, variable jaundice, splenomegaly and cholelithiasis. You just clipped esferocitosis hereditaria first slide! Rsferocitosis diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see herrditaria terms.
Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. Se recomienda el monitoreo de glucemia y ferritina. Reset dizgnostico links Resets both viewing and editing links coeditors shown below are not affected.
The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, esferocitosis hereditaria kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
See more popular or the latest esferocitosiis. The full herexitaria dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.
De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. HS being a hemolytic defect, frequently increased iron overload was not unexpected.
Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Laparoscopic splenectomy is preferred if performed by experienced surgeons. HI estudio de un caso de Esferocitosis Familiar. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.
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Polish Academjy of Sciences? Esferocitosis hereditaria cell morphology, osmotic resistance, hypertonic cryohemolysis test, esferocitosid binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide gel electrophoresis and ektacytometry are all used to diagnose HS. Check this box if you wish to receive a copy of your message.
Bienvenido a siicsalud Contacto Inquietudes. Exchange transfusion was performed in 3 children 1 with the severe form and 2 hhereditaria the typical form of the disease. Send link to edit together this prezi using Prezi Meeting learn more: Este hecho explica la discrepancia entre estos valores. Send the link below via email or IM Copy. Polish Academjy of Sciences? Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
Applying criteria such as permanence of an increased percentage of spherocytes, family history, biochemical symptoms of hemolysis and clinical data, we claim a prevalence of generally asymptomatic hereditary spherocytosis HS of 1: Summary and related texts. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.
Monitoring of blood glucose and ferritin is recommended. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.