ANEMIA OF ABNORMAL IRON METABOLISM Flashcards

1
Q

ANEMIA OF ABNORMAL IRON METABOLISM

A
  • Microcytic
  • Hypochromic
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2
Q

necessary for the synthesis of normal
oxygen carrying hemoglobin.

A

Iron

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3
Q

storage form of iron

A

SERUM FERRITIN

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4
Q
  • reflects the body tissue iron stores and thus a good indicator of iron storage status
A

SERUM FERRITIN

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5
Q

first laboratory test to become abnormal

A

SERUM FERRITIN

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6
Q

not helpful in the differentiation of IDA and Anemia of Chronic disorders because both have INCREASED values

A

FREE ERYTHROCYTE PROTOPORPHYRIN

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7
Q

measure how much the RBC can bind iron

A

TOTAL IRON BINDING CAPACITY (TIBC)

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8
Q

Transportation or iron throughout the body.

A

TRANSFERRIN SATURATION

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9
Q

Computed as:

A

Serum Iron/TIBC x 100

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10
Q

it is the last stage of iron deficiency

A

SERUM IRON

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11
Q

Men -
Post menopausal women -
Pregnant -

A

10mg/day
20mg/day
30 - 75mg/day

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12
Q

is a persistent, compulsive desire to eat a
single food or a non-food item such as starch or something crunchy such as ice, clay or plaster.

A

PICA

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13
Q

cracks in the corners of the mouth

A

Angular stomatitis

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14
Q

soreness of the tongue

A

Glossitis

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15
Q

flattening and spooning of the nails

A

Koilonychia

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16
Q

LABORATORY FINDINGS

A
  • Decreased Hgb, Hct and RBC
  • Decreased Indices
  • Microcytic, hypochromic
  • Elevated RDW
  • Variable platelet count
  • WBC and Reticulocyte count normal
17
Q

SHOULD BE DONE WITH _______

A

PRUSSIAN BLUE STAIN

18
Q

Hemoglobin values reach normal levels within

A

2 months

19
Q

Are a diverse group identified by a common feature of abnormal iron kinetics that produces excess accumulation of iron, which is deposited in the mitochondria of normoblasts

A

SIDEROBLASTIC ANEMIAS

20
Q

iron in the form of ferritin aggregates and at least 4 aggregates can be identified in approximately 50% of normoblasts

A

Type I

21
Q

contains 6 aggregates

A

type II

22
Q

pathologic ringed sideroblast

A

type III

23
Q

For a diagnosis of Sideroblastic anemia, at least

A

15% of normoblasts must be Type III ringed sideroblasts.

24
Q

ALA synthase deficiency

A

HEREDITARY (rare)

25
Q

cause is unknown, almost always related to anemia

A

Primary (idiopathic)

26
Q

Ex of primary

A
  • Acute myeloid leukemia
  • Myelodysplastic syndromes
  • Myeloma
27
Q

Drugs used in the treatment of tuberculosis

A
  • Isooniazid
  • Cycloserine
  • Pyrazinamide
28
Q

Occurs in children (ingestion of lead containing paint) and in adults (gasoline stations)

A

LEAD INTOXICATION

29
Q

deposit of iron in different organs of
our body.

A

Hemosiderosis

30
Q

ANEMIA OF ABNORMAL NUCLEAR DEVELOPMENT

A
  • Macrocytic
  • Normochromic
31
Q

represents 75% of cobalamin in the plasina

A

Adenosylcobalamin

32
Q

represents 75% of cobalamin in the liver robes, and the kidneys

A

Methylcobalamin

33
Q

is a rare X-linked disorder of purine metabolism caused by the lack of the enzyme xanthine-guanine phosphoribosyl transferase.

A

LESCH-NYHAN SYNDROME

34
Q

a rare hereditary autosomal recessive disorder of pyrimidine metabolism resulting in abnormal DNA synthesis, excessive urinary excretion of orotic acid, and megaloblastic anemia.

A

OROTIC ACIDURIA