Demonstration of Immune Complexes in Thrombotic Thrombocytopenic Purpura and Effect of Exchange Transfusion

2009 ◽  
Vol 24 (5) ◽  
pp. 373-380 ◽  
Author(s):  
Ronald A. SacherDr ◽  
Terence M. Phillips ◽  
George G. Shashaty ◽  
Robert J. Jacobson ◽  
Charles E. Rath ◽  
...  
1981 ◽  
Vol 7 (01) ◽  
pp. 25-32 ◽  
Author(s):  
Jerome Gottschall ◽  
Anthony Pisciotta ◽  
Joseph Darin ◽  
Clara Hussey ◽  
Richard Aster

Author(s):  
Maryam Darnahal ◽  
Hamed Azhdari Tehrani ◽  
Mohammad Vaezi ◽  
Shirin Haghighi

Endothelial injury by toxins, drugs, immune complexes leads to activation of coagulation cascade and thrombosis, which result in platelet consumption and red blood cell injury. These thrombotic microangiopathies can potentially injure numerous organs and result in organ dysfunction. In this case, we present the fourth reported patient with thrombotic thrombocytopenic purpura associated with COVID-19.


Blood ◽  
1979 ◽  
Vol 54 (4) ◽  
pp. 842-849 ◽  
Author(s):  
EG Taft

Abstract Four patients with thrombotic thrombocytopenic purpura (TTP) were treated by plasma-exchange transfusion, three of whom recovered completely. Because previous reports in the literature describing exchange transfusion as treatment for TTP have demonstrated variable success rates, particular attention was given to “dose”and frequency of plasma exchange. Evans blue dye studies established a measure of “dose” under conditions of varying efficiency. Serum LDH activity was found to be diminished by plasma exchange, and the rate of return of serum LDH activity reflected residual disease activity. The magnitude of LDH activity reduction correlated with the adequacy of dose of plasma exchange and was an indicator for the need of repeated daily exchanges. Failure to obtain a spontaneous increment in platelet count also suggested the need for additional exchanges and/or larger dose of exchange. There is a need for a standard expression of dose of plasma exchange. Utilizing these markers (LDH, platelet count), it may be possible to improve the survival in TTP if adequate dose and frequency of plasma exchange are used.


2015 ◽  
Vol 4 (1) ◽  
Author(s):  
Rachael Sutton ◽  
Andrew Will ◽  
Minju Kuruvilla ◽  
Suresh Victor

AbstractCongenital ADAMTS-13 deficiency is rare, with only between 150 and 200 living cases described internationally. It can present in the neonatal period with thrombocytopenia that may be associated with thrombosis rather than haemorrhage, microangiopathic haemolytic anaemia (MAHA) and jaundice requiring exchange transfusion. We report a case of a large cerebral infarction resulting from severe ADAMTS-13 deficiency in the immediate neonatal period. The diagnosis of ADAMTS-13 deficiency should be considered in babies with haemolytic anaemia, jaundice, thrombocytopenia and a negative direct antiglobulin (Coombs) test (DAT). It is important to diagnose and treat early in order to prevent further brain and kidney damage.


2014 ◽  
Vol 12 (3) ◽  
pp. 329-336 ◽  
Author(s):  
L. A. Lotta ◽  
C. Valsecchi ◽  
S. Pontiggia ◽  
I. Mancini ◽  
A. Cannavò ◽  
...  

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