Thrombotic thrombocytopenic purpura laboratory findings: Difference between revisions
Line 23: | Line 23: | ||
* '''Urine output:''' Decreased | * '''Urine output:''' Decreased | ||
* '''ADAMTS13 activity test:''' Decreased to < 10% during acute episodes of TTP. | * '''ADAMTS13 activity test:''' Decreased to < 10% during acute episodes of TTP. | ||
* ADAMTS13 inhinbitors test: | * '''ADAMTS13 inhinbitors test:''' | ||
* '''Genetic testing:''' Should be done in suspected cases | * '''Genetic testing:''' Should be done in suspected cases | ||
** Positive family history | ** Positive family history |
Revision as of 19:35, 24 August 2018
Thrombotic thrombocytopenic purpura Microchapters |
Differentiating Thrombotic thrombocytopenic purpura from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Thrombotic thrombocytopenic purpura laboratory findings On the Web |
American Roentgen Ray Society Images of Thrombotic thrombocytopenic purpura laboratory findings |
FDA on Thrombotic thrombocytopenic purpura laboratory findings |
CDC on Thrombotic thrombocytopenic purpura laboratory findings |
Thrombotic thrombocytopenic purpura laboratory findings in the news |
Blogs on Thrombotic thrombocytopenic purpura laboratory findings |
Directions to Hospitals Treating Thrombotic thrombocytopenic purpura |
Risk calculators and risk factors for Thrombotic thrombocytopenic purpura laboratory findings |
lease help WikiDoc by adding content here. It's easy! Click here to learn about editing.
Laboratory Findings
- CBC shows:
- Thrombocytopenia (median platelet count 10,000/microL)
- Microangiopathic hemolytic anemia [1]:
Hemolytic anemia |
---|
|
- Peripheral blood smear: Schistocytes, including helmet cells and triangular cells, polychromasia, microspherocytes and nucleated RBCs
- Urinalysis: Hematuria, proteinuria
- Serum creatinine: Increased
- Urine output: Decreased
- ADAMTS13 activity test: Decreased to < 10% during acute episodes of TTP.
- ADAMTS13 inhinbitors test:
- Genetic testing: Should be done in suspected cases
- Positive family history
- Recurrent episodes
- Onset during childhood or pregnancy
- Absence of inhibitors
- Persistent ADAMTS13 deficiency
- Imaging:
- Blood culture:
- Stool exam:
- Pathology: Tissue biopsy is not necessary for diagnosis, but it may show classic changes of a thrombotic microangiopathy including platelet microthrombi in small arterioles or capillaries, or hyaline changes in and around vessel walls.
References
- ↑ BRAIN MC, DACIE JV, HOURIHANE DO (1962). "Microangiopathic haemolytic anaemia: the possible role of vascular lesions in pathogenesis". Br J Haematol. 8: 358–74. PMID 14014893.