Hemoglobinopathies
Thalassemias
Cytochemical Stains
Leukemias / Lymphoproliferative Disorders
Misc
100

This occurs when valine replaces glutamic acid on position 6 on only one beta chain 

Sickle cell trait 


** SS disease is when it occurs on both beta chains

100

Thalassemias are the result of a  __________  (structural or quantitative) defect in the ________ portion of hemoglobin 

Quantitative / globin-chain


100

A patient has an extremely high WBC and a shift to the left is seen in the peripheral blood smear. The patient has an LAP score of 300. What is the most likely reason for these findings? 

Leukemoid reaction 


** LAP ( Leukocyte Alkaline Phosphatase Stain) important because patient labs can present very similar to CML but CML will have decreased LAP score as will AML 

100

This cell is suggestive of Hodgkin disease 

Pic #6

Reed-Sternberg Cell

100

___________ is a malignancy of the lymphoplasmacytoid cells, which manufacture IgM

Waldenström’s macroglobulinemia

200

What hemoglobinopathy has the following Hemoglobin % : 

3% A2

5% F

92% C 

Hgb C disease 

200

This is a Homozygous disorder caused by point mutation of the HBB gene on chromosome 11 and can result in the following Hgb pattern: 

Hgb A = 15-35%

 Hgb F = 60-90%

Hgb A2=  2-5%

Beta Thalassemia Major ( Cooley's anemia ) 

200

Naphthol AS-D chloroacetate esterase ( specific ) is usually positive in what cell line? 

Alpha-naphthyl acetate esterase ( non-specific) is positive in what cell line? 

Granulocytes / monocytes 

200

the WHO classification requires what percentage for the blast count in the blood or bone marrow for the diagnosis of AML

=/> 20% 


**FAB is 30% 

200

A 19-year-old man came to the emergency department with severe joint pain, fatigue, cough, and fever. Review the following laboratory results:

 WBCs 21.0 × 109/L            RBCs 3.23 × 1012/L Hgb 9.6 g/dL                      PLT 252 × 109/L Differential: 17 band neutrophils; 75 segmented neutrophils; 5 lymphocytes; 2 monocytes;               1 eosinophil; 26 NRBCs What is the corrected WBC cout? 

16.7 x 10 ( 9th) / L 


Total WBC × 100 or (21.0 × 100) ÷ 126 =

300

Patients with the sickle cell trait have a resistance to Malaria caused by what protozoa 

Plasmodium falciparum

300

This type of Thalassemia results in a mild anemia and the typical Hgb pattern seen here: 

Hgb A = 90%

Hgb F= 2-5%

Hgb A2 = 2-7%

Beta Thalassemia Minor 
300

This cytochemical stain is used to help differentiate Blasts of AML vs ALL .. it specifically stains positive blasts of AML and negative for ALL by staining lipids present

Sudan Black B 

300

In myelofibrosis, the characteristic abnormal red blood cell morphology is that of

teardrop / dacrocyte
300

Which antibody is associated with paroxysmal cold hemoglobinuria (PCH)

Anit-P 

400

A cellulose acetate electrophoresis revealed a large band of hemoglobin in the hemoglobin S portion. This band quantified at 95%. The peripheral smear revealed 70% target cells and the solubility test was negative. Based on this information what is the hemoglobin? 

Hemoglobin D 

400

Hemoglobin composed of 4 beta chains 

Hgb H 

400

Cells that exhibit a positive stain with acid phosphatase and are not inhibited with tartaric acid are characteristically seen in

Hairy Cell Leukemia 

400

myeloproliferative disorder characterized by uncontrolled proliferation of erythroid precursors. However, production of all cell lines is usually increased

Polycythemia vera

400

Osmotic fragility of Red cells is increased in situations where there is increase spherocytes like that seen in hemolytic anemia associated with hereditary spherocytosis .. however osmotic fragility test will be decreased in what disease state ? 

Sickle cell anemia 

500

In this hemoglobinopathy the patient Inherited Both Beta Chains with Substitution  glutamic acid replaced by lysine at position 6

Alpha2 Beta26glu      to       lys

Hemoglobin C disease 

500

Alpha thalassemia Major results in what 100% of what type of Hgb being formed ? 

Hgb Bart's - babies do not survive


* Hgb Barts = 4 gamma chains all 4 alpha chains deleted

500

Periodic acid schiff (PAS) stain performed on a bone marrow aspirate smear showed  abnormal (chunky globular) pattern of staining in the erythroblasts. This is suggestive of 

erythroleukemia

500

What cell besides lymphocytes do we typically seen increased in CML? 

Basophil

500

If a patient has a reticulocyte count of 7% and an

Hct of 20%, what is the corrected reticulocyte

count?

3.1% 

Corrected reticulocyte count = reticulocytes (%) × Hct ÷ 45

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