Hematology/Oncology_RR Flashcards

1
Q

Four causes of microcytic anemia

A
"TICS"
Thalassemia
Iron deficiency
anemia of Chronic disease
Sideroblastic anemia
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2
Q

An elderly man with hypochromic, microcytic anemia is asymptomatic. Which diagnostic tests should be ordered?

A

Fecal occult blood test and sigmoidoscopy

Suspect colorectal cancer

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3
Q

Precipitants of hemolytic crisis in patients with G6PD deficiency

A

Sulfonamides, antimalarial drugs, fava beans

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4
Q

The most common inherited cause of hypercoagulability

A

Factor V Leiden mutation

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5
Q

The most common inherited bleeding disorder

A

von Willebrand’s disease

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6
Q

The most common inherited hemolytic anemia

A

Hereditary spherocytosis

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7
Q

Diagnostic test for hereditary spherocytosis

A

Osmotic fragility test

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8
Q

Pure red blood cell aplasia

A

Diamond-Blackfan anemia

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9
Q

Anemia associated with absent radii and thumbs, diffuse hyperpigmentation, café au lait spots, microcephaly, and pancytopenia

A

Fanconi’s anemia

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10
Q

Medications and viruses that lead to aplastic anemia

A

Chloramphenicol, sulfonamides, radiation, HIV, chemotherapeutic agents, hepatitis, parvovirus B19, Epstein-Barr virus

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11
Q

How to distinguish polycythemia vera from secondary polycythemia

A

Both have increased hematocrit and RBC mass, but polycythemia vera should have normal O2 saturation and low EPO levels

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12
Q

What is the pentad for thrombotic thrombocytopenic purpura (TTP)

A
"FAT RN"
Fever
Anemia
Thrombocytopenia
Renal dysfunction
Neurologic abnormalities
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13
Q

What is the triad for hemolytic-uremic syndrome (HUS)?

A

Anemia
Thrombocytopenia
Acute renal failure

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14
Q

Treatment for TTP?

A

Emergent large-volume plasmapheresis, corticosteroids, antiplatelet drugs.
(Platelet transfusion is contraindicated.)

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15
Q

Treatment for idiopathic thrombocytopenic purpura (ITP) in children.

A

Usually resolves spontaneously; may require IVIG and/or corticosteroids

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16
Q
Which of the following is/are increased in DIC?
Fibrin split products,
D-Dimer,
Fibrinogen,
Platelets,
Hematocrit
A

Fibrin split products and d-dimer are elevated.

Platelets, fibrinogen, and hematocrit are decreased.

17
Q

An 8-year-old boy presents with hemarthrosis and an increased PTT with normal PT and bleeding time. Diagnosis? Treatment?

A
Hemophilia A or B
Consider desmopressin (for hemophilia A) or factor VIII or IX supplements
18
Q

A 14-year-old girl presents with prolonged bleeding after dental surgery and with menses, normal PT, normal or increased PTT, and increased bleeding time. Diagnosis? Treatment?

A

von Willebrand’s disease

Treat with desmopressin, fresh frozen plasma, or cryoprecipitate

19
Q

A 60-year-old African American man presents with bone pain. What might a workup for multiple myeloma reveal?

A

Monoclonal gammopathy, Bence-Jones proteinuria, “punched-out” lesions on x-ray of the skull and long bones

20
Q

In which condition are Reed-Sternberg cells seen?

A

Hodgkin’s Lymphoma

21
Q

A 10-year-old boy presents with fever, weight loss, and night sweats. Examination shows an anterior mediastinal mass. Suspected diagnosis?

A

Non-Hodgkin’s Lymphoma

22
Q

Microcytic anemia with decreased serum iron and ferritin, and increased TIBC?

A

Iron deficiency anemia

23
Q

Microcytic anemia with decreased serum iron and TIBC, and normal or elevated ferritin?

A

Anemia of chronic disease

24
Q

An 80-year-old man presents with fatigue, lymphadenopathy, splenomegaly, and isolated lymphocytosis. What is the suspected diagnosis?

A

Chronic lymphocytic leukemia (CLL)

25
What is the lymphoma equivalent of CLL?
Small lymphocytic lymphoma
26
A late, life-threatening complication of chronic myelogenous leukemia (CML)?
Blast crisis | Fever, bone pain, splenomegaly, pancytopenia
27
Auer rods on blood smear
Acute myelogenous leukemia (AML)
28
Which AML subtype is associated with DIC. Treatment?
AML M3 or APL. | Retinoic acid
29
Electrolyte changes in tumor lysis syndrome
Increased: Potassium, Phosphate, Uric Acid Decreased: Calcium
30
A 50-year-old man presents with early satiety, splenomegaly, and bleeding. Cytogenetics show t(9,22). Diagnosis?
CML
31
What are Heinz bodies?
Intracellular inclusions seen in thalassemia, G6pd deficiency, and postsplenectomy
32
Virus associated with aplastic anemia in patients with sickle cell anemia
Parvovirus B19
33
A 25-year-old African American man with sickle cell anemia has sudden onset of bone pain. Management of pain crisis?
O2, analgesia, hydration, and, if severe, transfusion
34
A significant cause of morbidity in thalassemia patients. Treatment?
Iron overload | Use deferoxamine