Red Blood Cell & Bleeding Disorders Flashcards

1
Q

All intrinsic types of hemolytic anemia are extravascular except for?

A

Paroxysmal Nocturnal Hemoglobinuria (PNH)

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2
Q

Which condition is under the intrinsic type of hemolytic anemia but exhibits both intra- and extravascular hemolysis?

A

Glucose-6-phosphate dehydrogenase (G-6PD) Deficiency

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3
Q

This disease is characterized by defects in membrane skeleton proteins, specifically spectrin, ankyrin, band 3 and Band 4,2.

A

Hereditary Spherocytosis

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4
Q

These are found in asplenic G6PD deficiency patients and are derived from hemoglobin?

A

Heinz bodies

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5
Q

These are found in asplenic sickle cell anemia patients and are composed of nuclear remnants.

A

Howell-Jolly Bodies

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6
Q

This disease is characterized by having 3 copies of the abnormal a-globin gene.

A

HbH disease

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7
Q

This type of immunohemolytic anemia occurs postinfection and is mainly due to IgM.

A

Cold agglutinin type

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8
Q

Name the two vitamins deficiency that cause macrocytic megaloblastic anemia?

A

Vitamin B12 & B9

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9
Q

What are the components of thrombotic thrombocytopenic purpura (TTP) ?
What cell product is decreased in this condition?

A
  1. Microangiopathic Hemolytic Anemia
  2. Thrombocytopenia
  3. Renal failure
  4. Fever
  5. Neurologic manifestations
  6. ADAMTS13
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10
Q

This is the most common adverse reaction of blood transfusion?

A

Febrile Non-hemolytic Transfusion Reaction (FNHTR)

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11
Q

What is called Christmas disease ? What is the clotting factor that is lacking in this condition?

A

Hemophilia B, Factor IX

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12
Q

This condition is characterized by bilateral adrenal hemorrhage secondary to fibrin thrombi?

A

Waterhouse - Freidrichsen Syndrome

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13
Q

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?

A

Paroxysmal Cold Hemoglobinuria

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14
Q

36/F known case of systemic Lupus Erythematous presents with easy fatigability. CBC shows reticulocytosis. Direct Coombs Test: Positive. What’s the diagnosis?

A

Autoimmune Hemolytic Anemia (AIHA)

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15
Q

Type of immune thrombocytopenic purpura seen in children after an acute infection, which resolves spontaneously.

A

Acute ITP

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16
Q

Type of genetic mutation that causes beta thalassemia?

A

Point mutation

17
Q

Causes anemia in sickle cell disease ?

A

Consumption of red cells by splenic macrophages

18
Q

Elevated hemoglobin 20g/L, Hct of 50% , WBC count of 15,000 and elevated platelet count of 400,000.

A

Polycythemia vera

19
Q

Panmyelosis is a characteristic of which type of blood cancer?

A

Polycythemia vera

20
Q

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?

A

Essential thrombocytosis