La púrpura trombótica trombocitopénica (PTT) o síndromede Moschcovitz es un síndrome clínico poco frecuente,menos incluso en la edad pediátrica que en la. Aka: Microangiopathic Anemia, Microangiopathic Hemolytic Anemia, Fragmentation Hemolysis, MAHA Italian, Anemia emolitica microangiopatica. Aka: Microangiopathic Anemia, Microangiopathic Hemolytic Anemia, Fragmentation Hemolysis, MAHA. See Also Italian, Anemia emolitica microangiopatica.

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Garrido aJ. Microangiopathic hemolytic anemia results in isolated increase in serum bilirubin levels. Content is updated monthly with systematic literature reviews and conferences. Iron-deficiency anemia Plummer—Vinson syndrome Macro-: In other projects Wikimedia Commons.

By using this site, you agree to the Terms of Use and Privacy Policy. Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia.

Estudio retrospectivo de 22 episodios consecutivos en 16 pacientes. Microangiopathic hemolytic anemia C Related links to external sites from Bing. Diseases of red blood cells D50—69,74— Please help improve this article by adding citations to reliable sources.

I risultanti schistociti sono fortemente captati per la loro distruzione dal sistema reticoloendoteliale nella milza, a causa dei loro stretti passaggi attraverso i microangiopaticw dei vasi ostruiti. Le informazioni riportate non sono consigli medici e potrebbero non essere accurate.


Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood. L’anemia emolitica microangiopatica determina un aumento isolato dei livelli sierici di bilirubina.

Hematology and Oncology Chapters. This cardiovascular system article is a stub. We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment.

You can help Wikipedia by expanding it. In all causes, the mechanism of MAHA is the formation of a fibrin mesh due to increased activation of the system of coagulation. Fanconi anemia Diamond—Blackfan anemia Acquired: Articles needing additional references from September All articles needing additional references Infobox medical condition All stub articles.

The resulting schistocytes red cell fragments are also increasingly targeted for destruction by the reticuloendothelial system in the spleen, due to their narrow passage through obstructed vessel lumina.

Anemia microangiopática

I contenuti hanno solo fine illustrativo microangiopatcia non sostituiscono il parere medico: It is seen in systemic lupus erythematosuswhere immune complexes aggregate with platelets, forming intravascular thrombi. From Wikipedia, the free encyclopedia. Le cause della condizione possono essere: Estella Aguado b wnemia. MAHA – Microangi haemoly anaemMicroangiopath haemolyt anaemMicroangiopathic hemolytic anemiaMHA-Microangiop haemolyt anaemmicroangiopathic hemolytic anemia diagnosismicroxngiopatica hemolytic anemiahemolytic microangiopathic anemiaMicroangiopathic Hemolytic AnemiaIsrael’s shunt hyperbilirubinemiaShunt hyperbilirubinemiaMAHA – Microangiopathic haemolytic anaemiaMAHA – Microangiopathic hemolytic anemiaMicroangiopathic haemolytic anaemiaMHA – Microangiopathic haemolytic anaemiaMHA – Microangiopathic hemolytic anemiaIsrael’s shunt hyperbilirubinaemiaMicroangiopathic hemolytic anemia disorderShunt hyperbilirubinaemiahemolytic; anemia, microangiopathicanemia; hemolytic, microangiopathic.


References Udden in Goldman Cecil Medicine.

Anemia emolitica microangiopatica

J Pediatr,pp. J Pediatr Hematol Oncol, 18pp. Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Retrieved kicroangiopatica ” https: Successful treatment of recurrent thrombotic thrombocytopenic purpura with plasmapheresis and vincristine.

Microangiopathic Anemia

You are currently viewing the original ‘fpnotebook. Megaloblastic anemia Pernicious anemia. Hematology and Oncology – Hemolytic Disorders Pages.

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