Difference between revisions of "Thrombotic thrombocytopenic purpura"

From Libre Pathology
Jump to navigation Jump to search
(create)
 
 
(8 intermediate revisions by the same user not shown)
Line 1: Line 1:
'''Thrombotic thrombocytopenic purpura''' is a type of [[thrombotic microangiopathy]].
'''Thrombotic thrombocytopenic purpura''', abbreviated '''TTP''', is a type of [[thrombotic microangiopathy]].


It was classically described as the pentad of:<ref>{{Ref PBoD8|669}}</ref>
==Classic pentad==
It was classically described as the pentad of:<ref name=Ref_PBoD8_669>{{Ref PBoD8|669}}</ref>
#Fever.
#Fever.
#Thrombocytopenia.
#Thrombocytopenia.
#Microangiopathic hemolytic anemia.
#Microangiopathic hemolytic [[anemia]].
#*Usu. with schistocytes (fragmented [[RBC]]s).<ref>{{Ref Klatt|65}}</ref>
#Transient neurologic symptoms.
#Transient neurologic symptoms.
#Renal failure.
#Renal failure.


Mnemonic: ''HUS/TTP is a CRAFTY syndrome'':<ref>URL: [http://www.valuemd.com/mnemonics2.php http://www.valuemd.com/mnemonics2.php]. Accessed on: 8 November 2010.</ref>
===Mnemonic===
''[[HUS]]/TTP is a CRAFTY syndrome'':<ref>URL: [http://www.valuemd.com/mnemonics2.php http://www.valuemd.com/mnemonics2.php]. Accessed on: 8 November 2010.</ref>
*'''C'''NS symptoms.
*'''C'''NS symptoms.
*'''R'''enal failure.
*'''R'''enal failure.
Line 14: Line 17:
*'''F'''ever.
*'''F'''ever.
*'''T'''hrombocytopenia.
*'''T'''hrombocytopenia.
*'''Y''' - no one knows "Y" it occurs.  
*'''Y''' - no one knows "Y" it occurs.
 
==Etiology==
Deficiency of plasma enzyme ''ADAMTS13'' which may be:<ref name=Ref_PBoD8_669>{{Ref PBoD8|669}}</ref>
*Inherited.
*Acquired (autoantibodies).


==See also==
==See also==
*[[Vasculitides]].
*[[Vasculitides]].
*[[Hemolytic uremic syndrome]].
*[[Medical renal diseases]].
*[[Medical renal diseases]].
*[[Anemia]].


==References==
==References==
Line 24: Line 34:


[[Category:Cardiovascular pathology]]
[[Category:Cardiovascular pathology]]
[[Category:Diagnosis]]

Latest revision as of 01:01, 28 February 2012

Thrombotic thrombocytopenic purpura, abbreviated TTP, is a type of thrombotic microangiopathy.

Classic pentad

It was classically described as the pentad of:[1]

  1. Fever.
  2. Thrombocytopenia.
  3. Microangiopathic hemolytic anemia.
    • Usu. with schistocytes (fragmented RBCs).[2]
  4. Transient neurologic symptoms.
  5. Renal failure.

Mnemonic

HUS/TTP is a CRAFTY syndrome:[3]

  • CNS symptoms.
  • Renal failure.
  • Anemia - microangiopathic hemolytic anemia.
  • Fever.
  • Thrombocytopenia.
  • Y - no one knows "Y" it occurs.

Etiology

Deficiency of plasma enzyme ADAMTS13 which may be:[1]

  • Inherited.
  • Acquired (autoantibodies).

See also

References

  1. 1.0 1.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 669. ISBN 978-1416031215.
  2. Klatt, Edward C. (2006). Robbins and Cotran Atlas of Pathology (1st ed.). Saunders. pp. 65. ISBN 978-1416002741.
  3. URL: http://www.valuemd.com/mnemonics2.php. Accessed on: 8 November 2010.