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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J Pediatr Hematol Oncol, 18pp. Examination Chapter related topics Plasmic Score. Fragmentation hemolysis and hypersplenismsu uptodate. As red blood cells travel through these damaged vessels, they are fragmented resulting in intravascular hemolysis.

Anemia microangiopática – Wikipédia, a enciclopédia livre

It is identified by the finding of anemia and schistocytes on microscopy of the blood film. Thefirst child recovered spontaneously. Unsourced material may be challenged and removed. Chronic relapsing thrombotic thrombocytopenic purpura: In other projects Wikimedia Commons.

Another, mobile version is also available which should function on both newer and older web browsers. Thrombotic microangopatica purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood. Continuing navigation will be considered as acceptance of this use. Menu di navigazione Strumenti personali Accesso non effettuato discussioni contributi registrati entra.


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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.

Related Bing Images Microngiopatica Microangiopathic hemolytic anemia and thrombocytopenia. Articles needing additional references from September All articles needing additional references Infobox medical condition All stub articles.


Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Da Wikipedia, l’enciclopedia libera.

Objective Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood. By using this site, you agree to the Terms of Use and Privacy Policy.

Microangiopathic Anemia

Familial infantile thrombotic thrombocytopenic purpura. Search Bing for all related images.

Back Links pages that link to this page. If you are using a modern web browser, you may instead navigate to the newer desktop version of fpnotebook. Med Clin Barc, pp. Please help improve this article by adding citations to reliable sources. Views Read Edit View history. Necesidades del alumnado con diabetes tipo 1 en Iron-deficiency anemia Plummer—Vinson syndrome Macro-: Gli eritrociti sono fisicamente tagliati da questa rete proteica e i frammenti sono identici agli schistociti visti al microangiopxtica ottico a luce trasmessa.


Fanconi anemia Diamond—Blackfan anemia Acquired: Le informazioni riportate non sono consigli medici e potrebbero non essere accurate. Estratto da ” https: The microangiopaatica diagnoses are rifampicin or probenecid microangiopafica, inherited disorders like Gilbert’s syndrome and other hemolytic disorders.

Hematology and Oncology Chapters. Nephrology Acquired hemolytic anemia Cardiovascular system stubs.

Hematology and Oncology – Hemolytic Disorders Pages. Evolution was favorable in both patients.

You can help Wikipedia by expanding it. Clinically, it is characterized by microangiopathic hemolyticanemia, thrombocytopenia, neurologic abnormalities,fever and renal dysfunction.