Red Blood Cell & Bleeding Disorders Flashcards
All intrinsic types of hemolytic anemia are extravascular except for?
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Which condition is under the intrinsic type of hemolytic anemia but exhibits both intra- and extravascular hemolysis?
Glucose-6-phosphate dehydrogenase (G-6PD) Deficiency
This disease is characterized by defects in membrane skeleton proteins, specifically spectrin, ankyrin, band 3 and Band 4,2.
Hereditary Spherocytosis
These are found in asplenic G6PD deficiency patients and are derived from hemoglobin?
Heinz bodies
These are found in asplenic sickle cell anemia patients and are composed of nuclear remnants.
Howell-Jolly Bodies
This disease is characterized by having 3 copies of the abnormal a-globin gene.
HbH disease
This type of immunohemolytic anemia occurs postinfection and is mainly due to IgM.
Cold agglutinin type
Name the two vitamins deficiency that cause macrocytic megaloblastic anemia?
Vitamin B12 & B9
What are the components of thrombotic thrombocytopenic purpura (TTP) ?
What cell product is decreased in this condition?
- Microangiopathic Hemolytic Anemia
- Thrombocytopenia
- Renal failure
- Fever
- Neurologic manifestations
- ADAMTS13
This is the most common adverse reaction of blood transfusion?
Febrile Non-hemolytic Transfusion Reaction (FNHTR)
What is called Christmas disease ? What is the clotting factor that is lacking in this condition?
Hemophilia B, Factor IX
This condition is characterized by bilateral adrenal hemorrhage secondary to fibrin thrombi?
Waterhouse - Freidrichsen Syndrome
5/F presents with fever , cough, and wheezing consistent with respiratory synctal virus infection. The patient has anemia and cola-colored urine. Donath-Landsteiner test is positive. What is the diagnosis?
Paroxysmal Cold Hemoglobinuria
36/F known case of systemic Lupus Erythematous presents with easy fatigability. CBC shows reticulocytosis. Direct Coombs Test: Positive. What’s the diagnosis?
Autoimmune Hemolytic Anemia (AIHA)
Type of immune thrombocytopenic purpura seen in children after an acute infection, which resolves spontaneously.
Acute ITP
Type of genetic mutation that causes beta thalassemia?
Point mutation
Causes anemia in sickle cell disease ?
Consumption of red cells by splenic macrophages
Elevated hemoglobin 20g/L, Hct of 50% , WBC count of 15,000 and elevated platelet count of 400,000.
Polycythemia vera
Panmyelosis is a characteristic of which type of blood cancer?
Polycythemia vera
48/F apparently asymptomatic. CBC : Platelet= 700 x 109/ L BM trephine: Normocellular marrow with megakaryocytic hyperplasia , megakaryocytes are morphilogically mature. Mutational analysis : JAK2(+). What is the diagnosis?
Essential thrombocytosis