Heme Part II Flashcards

1
Q

Anemia

A

Reduction in number or in quality or quantity of Hgb

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2
Q

Hemoglobin content low

A
Hypochromic
or normal (normochromic)
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3
Q

Anisocytosis

A

RBCs various sizes

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4
Q

Poikilocytosis

A

RBCs different shapes

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5
Q

Anemia Clinical manifestations

A
Hypoxia
Syncope
ANgina
Compensatory tachycardia 
Organ dysfunction.
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6
Q

Macrocytic-Normochromic

A
Megaloblastic anemia
cells unusually large
 DNA synthesis is defective
Usually due to deficiencies in
B12 or folate (B9)
• Co-enzymes for nuclear maturation and the DNA
synthesis pathway
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7
Q

Pernicious anemia

A

most common megaloblastic anemia
Lack of intrinsic factor Requires B12 absorption
Congenital or autoimmune
H pylori and PPI increase risk

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8
Q

Pernicious anemia S&S

A

Weakness, fatigue
paresthesia,
loss of appetite, abdominal pain, weight los

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9
Q

Atrophic glottis

A

Indicative of Pernicious anemia
B12 deficiency.
B9 cheilitis

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10
Q

Know picture of pernicious anemia

A

pernicious

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11
Q

Folate B9 deficiency

A

malnourishment

Neural tube defects

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12
Q

sphenocytes

A

RBCs shaped like a sphere.

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13
Q

Abnormal small cells with pale color

A

Microcytic-hypochromic anemia

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14
Q

Causes of microcytic-hypocrhomic anemia

A

Disorders of iron metabolism

porphyrin

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15
Q

Microcytic hypochromic

A

Cause Cutaneous porphyria

Caused by defective heme production

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16
Q

most common type of anemia is

A

Iron-deficiency

17
Q

Iron deficiency causes by

A

ASA
NSAIDS
insufficient iron intake

18
Q

S and symptoms of iron deficiency anemia

A

Pale conjunctiva
Fatigue,weakness
KOILONYCHIA nails (spoon shaped fingernails)

19
Q

Sideroblastic anemia

A

Defect in mitochondrial heme synthesis
iron precipitation
Acquired or hereditary
cline: iron overload

20
Q

Normocytic normochromic anemia

A

Normal size and hemoglobin content but low number

21
Q

Aplastic

A

Autoimmune
Chemical exposure
Chemotherapy drugs

Good marrow to nonfunctional yellow marrow

22
Q

Hereditary thalassemia

A

Acute blood loss

23
Q

Hemolytic anemia

A

Accelerated destruction of RBCs
Congenital versus acquired
Intravascular versus extravascular hemolysis
Paroxysmal nocturnal hemoglobinuria

24
Q

Hemolytic anemia

associated with Paroxysmal nocturnal Hemoglobinuria

A

Deficiency in CD55 and CD59 (MAC inhibitory
protein): Cause complement-mediated intravascular
lysis and release of hemoglobin
• Anemia, hemoglobinuria, severe fatigue, abdominal pain, and thrombosis

25
Q

G6PD

A

Protect RBCs from oxidative stress.

26
Q

Polycythemia vera

A

Splenomegaly

Treatment: Phlebotom 300-500ml to reduce erythrocytosis and

27
Q

Acute (children)

A

High proportion of immature

28
Q

Chronic

A

high proportion of mature

29
Q

Leukemia

A

PETECHIA
PURPURA

bone pain

30
Q

Multiple myeloma

A

Increased production of plasma cells

Pathological fracture

31
Q

Urine for Multiple myeloma

A

Bence jones cells

32
Q

Hodgkins lymphoma

Non-Hodgkins

A

Single lymph node

Multiple lymph nodes