Oncology Flashcards

1
Q

what is the most common hemolytic disorder in children

A

anemia
(the iron deficiency one is most common)

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2
Q

if hemoglobin in child is low, recomend ___

A

high iron diet

-NO extra milk tho, doesnt have iron

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3
Q

top 2 signs and symptoms of anemia, but still list the others

A

Tachypnea and Tachycardia!!!!

pallor, weakness and fatigues, irritability

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4
Q

anemia interventions

A
  • RBC administration
  • supplemental oxygen
  • administer Epogen (stimulates production of RBCs)
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5
Q

examples of situations that cause anemia caused by inadequate supply or loss of iron

A

-rapid growth rate
- excessive milk intake.delayed addition of solid foods
- exclusive breastfed infant after age 6 months

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6
Q

what disorders are the most common cause of anemia

A

malabsorption disorders (GI)

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7
Q

Lab work for anemia

A

CBC, Reticulocyte count (immature RBCs)

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8
Q

what lab results would indicate improvement in anemia treatment

A

high reticulocyte count

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9
Q

what lab is MOST reliable/indicative of anemia (on exam fo sho)

A

Ferritin (protein that stores iron in blood)

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10
Q

Treatment for Anemia

A

-Add iron rich foods
-oral supplements : ferrour iron 3-6mg/kg

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11
Q

things to think aboutif giving iron to kids with anemia

A

-drink through straw bc it stains teeth
- take with fruit juice (orange is best)
- 3-6mg/kg per day

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12
Q

what are the 10 iron rich foods

A
  1. Red meat
  2. liver
  3. giblets
    4.prunes
    5.artichokes
  4. iron fortified cereals
  5. egg yolks
  6. shelfish (clams, scallops)
  7. dark leafy greens
    10.legumes
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13
Q

how is sickle cell inherited

A

AUTOSOMAL RECESSIVE

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14
Q

what is sickle cell

A

hemoglobin disorder that causes normal round cells to change to crescent shape

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15
Q

clinical manifestations of sickle cell (what would a patient present with)

A

pallor, weakness, jaundice, tissue hypoxia

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16
Q

abnormal lab findings for sickle cell

A

decreases HgB
Increased Plt
high reticulocyte
high bilirubin

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17
Q

sickle cell treatments

A

-packed red blood cells
- hydroxyurea (increases production of fetal hemoglobin which helps reduce sickling of RBCs)
- pain management

18
Q

what is the only curative treatment of sickle cell

A

bone marrow transplant

19
Q

Vaso-Occlusive crisis

A

masses of sickle RBCs occlude vessels resulting in thrombosis, ischemia, and infarction

20
Q

Life threatening ocmplications of sickle cell

A
  • infection/sespsis
  • splenic sequestration (acute splenic enlargement from pooling of
  • acute chest syndrome (infection, can cause pulmonary infarction or htn)
21
Q

in order for a child to have sickle cell: parents___

A

were both carriers for SS trait

22
Q

what are triggers for a vasocclusive crisis in child with SS

A

dehydration, infection, fever, cold temp

23
Q

what is Idiopathic Thrombocytopenia Purpura

A

autoimmune thrombocytopenia
(low platelet count due to destruction of platelets by immune system)

24
Q

sympptoms and lab findings of ITP

A
  • petichae, epistaxis (nosebleeds), hematuria, bloody stool
  • lab: abnormal coagulation labs, low platelet count
25
treatment for ITP
steroids for inflammation, IVIG, drugs to boost platelet counts
26
transmissionof hemophilia
x-linked (more commonin males)
27
treatment of hemophilia
recombinanct factor 8 or 9 infusions
28
what is hemophilia
hem a: clotting factor 8 deficiency hem b:clotting factor 9 deficiency
29
what causes childhood cancer
unknown usually related to peak growth periods
30
what is the most commontypeofchildhood cancer
leukemia
31
name a risk factor in developing pediatric cancer
environemnt, genetic, past history, down syndrome
32
what is the role of platelets
clot
33
name some clinical symtoms of a brain tumor
headache, vomiting, nystagmus, increased ICP, bulging fontanels in newborns
34
When are children screened for sicklecell disease
birth
35
Whilm's tumor
tumor in kidney mostcommon in 2-3 year olds
36
Neuroblastoma
cancer that develops fromimmature nerve cells (neuroblasts) typically in adrenal glands - usually diagnosed at 19 months (1.5 years)
37
Osteocarcoma, what is it and which age group most popular
most commonin teens because rapid bone growth bone tumor that originates in bone forming cells (osteoblasts)
38
pathophysiology of leukemia
genetic damage to single bone marrow cell - causes uncontrolled multiplication of immature cells (blasts)
39
children with this genetic order are at higher risk for which cancer
down syndrome for leukemia
40
hodgkins vs nonhodgkins
localized vs. spreads (more common)
41
treatment for lymphoma
autologous or allogenic stem cell transplant