Hematology/Oncology Flashcards

1
Q

What finding on physical exam is a contraindication to aspirin use?

A

Nasal polyps 2/2 hypersensitivity reactions particularly in those with asthma, resulting in as asthma attack

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2
Q

Acanthocytes and spur cells

A

Abeta-lipo-proteinemia, 2/2 inability to synthesize apolipoprotein B, component of chylomicrons and VLDL so lipids absorbed by small intestine cannot be transported into blood & accumulate in intestinal epithelium resulting in erythrocyte with spike and foamy cytoplasm.

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3
Q

Echinocytes or burr cells

A

Hallmark of uremia, pyruvate kinase deficiency, microangiopathic hemolytic anemia or mechanical damage

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4
Q

Rouleaux formation

A

Stacked RBCs seen in multiple myeloma

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5
Q

Sideroblastic anemia

A

Iron inclusions in RBCs of the bone marrow

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6
Q

Causes of microcytic anemia with normal or elevated reticulocytes

A

Thalassemia or hemoglobinopathy (sickle cell disease)

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7
Q

Causes of microcytic anemia with low reticulocyte count

A

Lead poisoning
Sideroblastic anemia
Anemia of chronic disease

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8
Q

Plummer-Vinson syndrome

A
Esophageal webs (dysphagia)
Iron deficiency anemia 
Glossitis
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9
Q

Alcoholic with tea and toast diet is expected to have what vitamin deficiency?

A

Folate deficiency

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10
Q

Most common cause of Vitamin B12 deficiency

A

Pernicious anemia, 2/2 antiparietal cell antibodies that interfere with secretion of intrinsic factor by parietal cells which bind to B12 and allow for absorption i the ILEUM (B12-IF complex); Commonly p/w Achlorhydia

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11
Q

How to differentiate thalassemia from iron deficiency since both p/w microcytic hypochromic anemia?

A

Iron levels are normal in thalassemia. Look for elevations in hemoglobin A2 or Hemoglobin F (beta type)

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12
Q

“Crew-cut” on skull XR

A

Marrow expansion resulting skeletal deformities in beta thalassemia major

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13
Q

Who commonly gets Thalassemia?

A

Black persons or people of Mediterranean populations (Italian)

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14
Q

Treatment of minor thalassemia?

A

Usually asymptomatic

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15
Q

Treatment of major thalassemia?

A

Transfusions and iron chelation therapy to prevent secondary hemochromatosis

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16
Q

If you are given an increased MCHC.. think

A

Hereditary spherocytosis.

17
Q

PT measures function of…

A

Extrinsic clotting pathway, consists of VII (prolonged by warfarin)

18
Q

PTT measure function of…

A

Intrinsic clotting pathway, consists of 12, 11 9, 8 (prolonged by heparin)

19
Q

BT measures….

A

Platelet function (prolonged by aspirin)