Anemia acquisita da ospedalizzazione: il ruolo delle perdite di sangue a scopo .. di porpora trombotica trombocitopenica (sindrome di Moschcowitz). Thrombotic thrombocytopenic purpura (TTP or Moschcowitz syndrome) is a rare disorder of the blood Missing: di. malattia di Fabry, sindrome di Hunter, malattia di Gaucher, malattia di Pompe,. Sanfilippo e la leucodistrofia La sindrome di Hunter con una prevalenza stimata di su nota anche come Moschcowitz disease. Chronic beryllium.
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Drugs and bacteria have been implicated as etiologic factors. Differential diagnosis[ edit ] TTP is characterized by thrombotic microangiopathy TMAthe formation of blood clots in small blood vessels throughout the body, sindrome di moschcowitz can lead to microangiopathic hemolytic anemia and thrombocytopenia.
This characteristic is shared by two related syndromes, hemolytic-uremic syndrome HUS and atypical hemolytic uremic syndrome aHUS.
The introduction of plasma exchange has significantly lowered the mortality rate. In chronic kidney disease CKDthe estimated glomerular filtration rate eGFR based on serum creatinine in most cases is the best indicator of renal function, provided that creatinine is measured with sindrome di moschcowitz accurate enzymatic method.
In borderline situations, a confirmatory eGFR calculation based on cystatin C is recommended.
The contemporaneous measurement of free FT3, free FT4 and TSH, except for specific cases, should be discouraged due to the high frequency sindrome di moschcowitz unjustified abnormal findings. Anti-thyroperoxidase antibodies are the test of choice for autoimmune thyroid diseases.