MedComplex-Exam 3 Part 1 (SickleCell,PA,FolateAnemias) Flashcards

1
Q

What is the most common type of MEGALOBLASTIC anemia?

A

Pernicious Anemia

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2
Q

What type of anemia is Pernicious anemia?

A

Megaloblastic anemia

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3
Q

Pernicious anemia is a CHRONIC condition caused by malabsorption of _______, usually due to a lack of gastric _________, needed for absorption.

A

Vitamin B12 (in the small intestine), intrinsic factor

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4
Q

Pernicious Anemia is Most common in _____ adult life and is rare under the age of ____.

A

LATE….30

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5
Q

Where are the three most common areas to see Pernicious Anemia?

A

England, Ireland, Scandinavia

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6
Q

How do you test for Pernicious Anemia?

A

The (Curt) Schilling Test (The bloody sock test)

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7
Q

What is the substance tested for in a (curt) Schilling test for pernicious anemia? Which bodily fluid is looked at in this test?

A

Cobal-Amine (uh aka Vit B-12)…Urine (pt given cobalamine-it cannot be absorbed ORALLY by the PA patient-and then its peed out)

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8
Q

What is a prussian blue test looking for?

A

Iron deficiency anemia

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9
Q

What is another name for an IRON stain? What color does it stain the iron?

A

Prussian Blue

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10
Q

Which condition will the histo show HYPERSEGMENTATION of Neutrophils and Basophilic Stippling of the RBCs?

A

Pernicious Anemia

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11
Q

In hyper segmentation of neutrophils, how many nuclear segments are shown? How many are normal?

A

5-6 are shown whereas only 3-4 are normal

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12
Q

In a megaloblastic anemia which cells will be hyperhsegmented and which cells will show basophilic stippling?

A

hyperhsegmented NEUTROPHILS and basophilic stippling of RBCs

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13
Q

What amount of people with Pernicious Anemia have CNS lesions? What degeneration can this lead to?

A

3/4 have CNS lesions..can lead to SUBactue Combined degeneration (loss of vibratory sense)

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14
Q

What is the tongue manifestation of pernicious anemia?

A

red-beefy tongue w loss of papillae

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15
Q

What is the only difference in the presentation of Pernicious Anemia and Folic Acid deficiency?

A

FA does not have the CNS effects

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16
Q

What are the two most common cause of anemia? What is second?

A

Iron deficiency….thalassimia

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17
Q

Sickle cell anemia is caused by a genetic defect in the synthesis of the _____ chain of hemoglobin.

A

BETA

18
Q

Sickle cell anemia: Substitution of ________ by _____ at the ___th position of the _____ chain.

A

Glutamic Acid by Valine…6th position…beta chain

19
Q

In Sickle Cell Anemia: The abnormal beta chain still combines with alpha chains, but instead of normal Hgb A, an abnormal _____ is formed.

A

Hgb S

20
Q

What type of electrophoresis is used in the diagnosis of Sickle cell anemia?

A

Hemoglobin Electrophoresis (not a protein electrophoresis) (NOT a plasma electrophoresis) (Hgb S migrates differently than Hgb A)

21
Q

What group of people is most affected by Sickle Cell Anemia? What group of people is NOT as affected?

A

African Americans and Africans affected.. Meditarrainian’s not affected (thalassemia)

22
Q

Like 3 questions for Sickle Crisis: What aggravates it (3)? Can they occur spontaneously?

A

aggravated by Fever, Respiratory Disease or Hypoxia…YES they can occur spontaneously

23
Q

Like 3 questions for Sickle Crisis: all situations characterized by ___________ can induce a sickling crisis

A

reduced oxygen tension

24
Q

Like 3 questions for Sickle Crisis: What 3 activities/life events can cause a crisis?

A

Mountain climbing, strenuous exercise…pregnancy

25
Q

Like 3 questions for Sickle Crisis: What is a characteristic feature in children?

A

DACT-YL-ITIS (swelling of dorsum of hands and feet)

26
Q

Complications of Sickle Cell Anemia: _______ of the skull due to bone marrow hyperplasia with “_______” appearance on skull X-ray.

A

BOSSING…“hair on end”

27
Q

Complications of Sickle Cell Anemia: _________ are common and cause visual problems.

A

Retinal infarcts

28
Q

Complications of Sickle Cell Anemia: What is the root cause of “Hair on End” appearance on the skull X-ray?

A

due to Bone Marrow Hyperplasia

29
Q

Complications of Sickle Cell Anemia: Which organ becomes fibrotic and shrinks? What is the clinical term for this?

A

the spleen…autosplenectomy

30
Q

Complications of Sickle Cell Anemia: Hemolysis results in WHAT 2 events in the liver? The increased excretion of WHAT?? in bile leads to the formation of _______.

A

hyperbilirubinemia and jaundice..Bilirubin…..bile stones

31
Q

Complications of Sickle Cell Anemia: Foci of _______ necrosis, which heals by fibrous scarring can be detected in ALL organs.

A

ischemic

32
Q

Complications of Sickle Cell Anemia: Retarded intellectual development, a consequence of brain ischemia and infarcts, the larger infarcts may cause a ______ syndrome.

A

stroke

33
Q

Complications of Sickle Cell Anemia: The attempts of the heart to compensate for inadequate oxygen transport results in cardiac ________ and ultimately, heart failure.

A

hypertrophy

34
Q

Complications of Sickle Cell Anemia: The occlusion of small peripheral blood vessels with sickled cells and thrombi aggravates the circulatory situation even more by increasing the __________.

A

peripheral resistance (blood pressure)

35
Q

Complications of Sickle Cell Anemia: Pulmonary _____ is common due to the heart failure, and it tends to predispose to patients to PNEUMONIA.

A

edema

36
Q

Complications of Sickle Cell Anemia: Infections are facilitated by changes in the ______ and _____.

A

SPLEEN and LIVER

37
Q

Complications of Sickle Cell Anemia: Other infections are common and recurrent, and usually involve foci of aseptic _____ necrosis, infarcts of internal organs, and ischemic skin ulcers.

A

BONE

38
Q

Complications of Sickle Cell Anemia: Both the spleen and liver are overloaded with _________ derived from hemolyzed red cells.

A

hemosiderin

39
Q

What is the most common cause of a FOLATE deficiency?

A

pregnancy

40
Q

Pregnancy is the most common cause of a ______ deficiency, but its only a minor cause in a ______ deficiency.

A

folate….Vit B12