Peds - Hematologic Flashcards

1
Q

What can early ingestion of cow’s milk cause?

prior to 9 months

A

micro-hemorrhage from the gut, leading to anemia

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2
Q

What can lead to iron deficiency anemia in toddler’s?

A

Reliance on whole milk at the expense of solid food.

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3
Q

What nail changes may be associated with anemia?

A

flat, brittle, or spoon-shaped nails

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4
Q

Laboratory findings in IRON DEFICIENCY ANEMIA

A
MCV - low (microcytic)
MCHC - low (hypochromic)
RDW - increased
TIBC - increased (available slots)
Serum ferritin - low (stores)
Serum iron - low
Reticulocyte count - low if low Fe is cause, hi if bleeding, or in thalassemia
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5
Q

Which anemias tend to be found in children?

A

MICROcytic - HYPOchromic (small cell, less color)

Iron deficiency anemia (IDA)
Thalassemia
Lead poisoning
G6PD deficiency

NORMOcytic, NORMOchromic can too

acute blood loss
early IDA

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6
Q

Which anemias tend to be found in adults?

A

MACROcytic, NORMOchromic

B12 deficiency
folate deficiency
pernicious anemia

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7
Q

Treatment for iron deficiency anemia

A

Elemental iron until HEMOGLOBIN normalizes
AND
Replace iron stores with supplementation x 4 months

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8
Q

IRON OVERLOAD can cause what two serious conditions?

A

cirrhosis

cardiomyopathy

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9
Q

What can giving iron to a person with Thalassemia cause?

A

Iron overload

they don’t have the binding sites to use the extra iron

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10
Q

Laboratory findings in Thalassemia that differ from IDA.

A

Reticulocyte count is increased

TIBC is low (no open slots, hence risk for iron overload)

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11
Q

Thalassemia is typically seen in what populations?

A

Mediterranean

Asian

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12
Q

Treatment for thalassemia

A

Refer to hematology

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13
Q

Genetics variations of sickle cell -

which is carrier which is symptomatic?

A

HOMOzygous - Hgb SS - symptomatic

HETEROzygous - Hgb AS - carrier, usually no clinical symptoms

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14
Q

Features of blood work findings in sickle cell? (4)

A

o nucleated RBCs
o reticulocytosis (10-25%)
o Howell-Jolly bodies
o WBCs elevated

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15
Q

Support for sickle cell crisis (5)

A
o  hydration
o  oxygen
o  analgesics
o  antibiotics
o  transfusion
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16
Q

What medication can be given to stimulate fetal hemoglobin (which doesn’t sickle)?

A

Hydroxyurea

17
Q

What supplement is important for those with sickle cell?

A

folic acid

18
Q

Which anemia can lead poisoning lead to?

A

iron deficiency anemia

19
Q

Where does the body store lead?

A

bone marrow

20
Q

At what point is chelation therapy used for lead poisoning?

A

Class IV: 45-69 mcg/dL

21
Q

A group of malignant hematological diseases in which normal bone marrow elements are replaced by abnormal, poorly differentiated lymphocytes known as blast cells.

A

Leukemias

22
Q

Is bone and joint pain an early or a late sign in leukemia?

A

late sign

23
Q

What are red flags for leukemia?

A

Lympadenopathy and hepatosplenomegaly

especially with recent fatigue, bleeding, and frequent infection

24
Q

Which is the most common leukemia in children?

A

ALL - Acute Lymphocytic Leukemia = 70%

25
Q

Epidemiology of pediatric ALL?

A

peak age 4 years
white
more boys than girls

26
Q

Acute myelogenous leukemia occurs more commonly at which ages?

A

Infant and older children