Hematology Flashcards

1
Q

True or False:
At birth, in a normal full term, they have lower hemoglobin and hematocrit and smaller RBCs.

A

False. Higher hemoglobin and hematocrit and bigger RBCs

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2
Q

True or False:
At birth, in a normal full term, they have lower hemoglobin and hematocrit and smaller RBCs.

A

False. Higher hemoglobin and hematocrit and bigger RBCs

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3
Q

True or false:
There is physiologic anemia of infancy after the first week of lofe until 6 to 8 weeks.

A

True

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4
Q

The most widespread and common nutritional disordee in the world

A

Iron Deficiency

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5
Q

True or False:
Hemoglobin falls during the first 2 - 3 months

A

True

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6
Q

Iron deficiency anemia:

A

Decreased serum ferritin
Decreased serum iron
Increased iron binding capacity
Serum transferrin increases (then)
Decreased transferrin

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7
Q

Iron deficiency anemia:

A

Decreased serum ferritin
Decreased serum iron
Increased iron binding capacity
Serum transferrin increases (then)
Decreased transferrin

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8
Q

The most important clinical sign of iron deficiency but is only evident if hemoglobin falls to 7 - 8 g/dL

A

Pallor

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9
Q

The most concerning effects in infants and adolescents are impaired intellectual and motor functions before anemia develops

A

Iron deficiency anemia

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10
Q

Microcytic anemia:

A

IDA
Thalassemia
Hemoglobinopathies

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11
Q

Microcytic anemia:

A

IDA
Thalassemia
Hemoglobinopathies

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12
Q

IDA

A

Decreased Ferittin
Decreased Serum Iron
Increased Total Iron Binding Capacity

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13
Q

IDA

A

Decreased Ferittin
Decreased Serum Iron
Increased Total Iron Binding Capacity

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14
Q

Noted increased RBCs and Normal RDW (Rbc distribution width)

A

Thalassemia

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15
Q

Daily dose of elemental iron in IDA:

A

3-6mg/kg of Elemental Iron in 3 Divided Doses

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16
Q

IDA correction, repeat CBCP during this time and will be observed to havd at least 1-2 g/dL increase in hemoglobin or has normalized already

17
Q

Iron medication is continued until when to re establish iron stores:

18
Q

A genetoc disorder in globin chain production with ineffective erythropoiesis

A

Thalassemia

19
Q

The marrow is hyperactive bit there are only a few reticulocytes nd severe anemia

A

Thalassemia

20
Q

Laboratory findings in Thalassemia:

A

Elevated unconjugated serum bilirubin
High ferittin and Transferrin

21
Q

Causes these two clinical syndrome: episodic hemolytic anemia and chronic non-spherocytic hemolytic anemia

A

G6PD Deficiency

22
Q

The blood may reveal precipitated hemoglobin (Heinz Bodies)

A

G6PD Deficiency

23
Q

Hallmark of hemophilic bleeding:

A

Hemarthrosis

24
Q

This condition is associated with hypoxia, acidosis, tissue necrosis, shock and or endothelial damage

A

Disseminated Intravascular Coagulopathy

25
In a previously healrhy 1-4 year old child, with sudden onset of generalized petechiae and purpura usually with a history of infection prior to onset of symptoms
Idiopathic Thrombocytic Purpura
26
Splenecromy in children with ITP:
More rhan 4 years old and severe ITP in a years Life threatening hemorrhage
27
Splenecromy in children with ITP:
More rhan 4 years old and severe ITP in a years Life threatening hemorrhage