Hema lect Flashcards
In HS, a characteristic abnormality in the CBC results is:
c. Increased MCHC
The altered shape of the spherocyte in HS is due to:
A mutated RBC membrane protein affecting vertical
protein interactions
Which one of the following sets of results is consistent with HS?
c. Increased osmotic fragility, negative DAT result
The RBCs in HE are abnormally shaped and have unstable cell membranes as a result of:
Defects in horizontal membrane protein interactions
The peripheral blood film for patients with mild HE is char- acterized by:
Elliptical RBCs
Laboratory test results for patients with HPP include all of the following except:
Increased MCV and normal RDW
Acanthocytes are found in association with:
Abetalipoproteinemia
The most common manifestation of G6PD deficiency is:
Acute hemolytic anemia caused by drug exposure or
infections
A patient experiences an episode of acute intravascular hemolysis after taking primaquine for the first time. The physician suspects that the patient may have G6PD defi- ciency and orders an RBC G6PD assay 3 days after the he- molytic episode began. How will this affect the test result?
False increase in enzyme activity due to reticulocytosis
The most common defect or deficiency in the anaerobic
glycolytic pathway that causes chronic HNSHA is:
Pyruvate kinase deficiency
Which of the following laboratory tests would be best to confirm PNH?
Flow cytometry for FLAER binding, CD24 on granulo-
cytes, and CD14 on monocytes
. A 22-year-old man with a moderate decrease in hemoglo- bin level and a decrease in RBC, WBC, platelet, and reticu- locyte counts has a history of infrequent and mild episodes of hemolysis with hemoglobinuria. His bone marrow showed 15% cellularity with no abnormal cells, and flow cytometry revealed that 15% of his circulating granulocytes were GPI deficient. He most likely has:
Hypoplastic PNH
Which one of the following is a feature found in all micro-
angiopathic hemolytic anemias?
Intravascular RBC fragmentation
Typical laboratory findings in TTP and HUS include:
Schistocytosis and thrombocytopenia
The pathophysiology of idiopathic TTP involves:
Formation of platelet-VWF thrombi due to autoantibody
inhibition of ADAMTS13