Pediatric Cancer Flashcards

(30 cards)

1
Q

Warning signs of blood cell cancers.

A

s/s of anemia,
activity intolerance,
infections

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2
Q

Warning signs of tumor cancers.

A

palpable mass,
discomfort/pain,
severe wt loss,
neurologic symptoms (paresthesia)

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3
Q

Briefly describe a neuroblastoma.

A

a neuro-endocrine tumor in the adrenal gland or sympathetic ganglia

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4
Q

Briefly describe how neuroblastoma presents.

A

Mass in abdomen or chest,
bone pain,
bruising around eyes

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5
Q

Identify other s/s associated with neuroblastoma.

A

abdominal distention,
anorexia, wt loss,
GI & GU dysfunction,
hepatosplenomegaly

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6
Q

Diagnostic imaging for neuroblastoma.

A

Ultrasound for abdomen OR X-ray for chest,
CT, MRI,
MIBG scan

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7
Q

Briefly describe the MIBG scan.

A

specific scan for neuroendocrine tumors; tumors show as dark regions

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8
Q

Identify lab testing for neuroblastomas.

A

24h urine collection to look for “vanilla” catecholamines

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9
Q

Briefly identify complications of neuroblastomas.

A

metastasis to lymph nodes,
nerve compression leading to neurological deficits

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10
Q

Briefly describe retinoblastoma.

A

A malignant tumor in the retina.

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11
Q

Identify key sign of retinoblastoma.

A

Leukocoria
aka the “cat’s eye reflex”
(pupil shines white with light)

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12
Q

Identify other s/s of retinoblastoma.

A

strabismus,
vision loss,
orbital inflammation,
proptosis

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13
Q

Briefly define strabismus.

A

cross-eyed

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14
Q

Briefly define proptosis.

A

Abnormal protrusion/bulge of the eye.

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15
Q

Identify the chief goal of treatment for retinoblastoma.

A

preserve the eye and vision,
protect the remaining eye!

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16
Q

Briefly define enucleation.

A

removal of the eye

17
Q

Briefly describe initial presentation of a Wilms tumor.

A

(aka nephroblastoma)

a unilateral firm abdominal mass (without any other symptoms yet)

18
Q

Identify key thing when assessing for a nephroblastoma.

A

(aka Wilms tumor)

DO NOT PALPATE THE ABDOMEN!

19
Q

Identify key complications of a Wilms tumor.

A

(aka nephroblastoma)

seeding - ruptures easily to metastasize to the lungs, brain, bones, and lymph nodes

20
Q

Identify key s/s of Wilms tumor.

A

(aka nephroblastoma)

asymmetry in abdomen,
abdominal discomfort,
s/s of kidney damage:
HTN due to renin production,
hematuria

21
Q

Most common medication for kidney-related symptom of a nephroblastoma.

A

(aka Wilms tumor)

ACE inhibitors for the hypertension

22
Q

Labs to monitor with Wilms tumor.

A

(aka nephroblastoma)

Kidney things:
BUN/creatinine,
K+ (hyperkalemia)

23
Q

Key pt teaching for nephroblastoma.

A

(aka Wilms tumor)

No contact sports (worried about seeding if tumor reoccurs).

24
Q

Briefly describe an osteosarcoma.

A

a large, tender soft tissue mass near the growth plate of a long bone

25
Identify risk factors for an osteosarcoma
growth spurt around 13-16yo, recent injury, Hx of radiation/chemo, female
26
s/s of osteosarcoma
localized pain lasting months, soft tissue swelling, limping, pathological fracture
27
Identify some long-term concerns with osteosarcoma.
reoccurrence, metastasis, poor body image, halted limb growth
28
Identify labs for osteosarcoma.
elevated alkaline phosphate (byproduct of bone formation), elevated ESR (indicating inflammation)
29
Identify imaging for osteosarcoma.
X-ray showing woven bone matrix "sun burst" pattern, CT, MRI, bone scan
30
Identify key treatment options for osteosarcoma.
chemo to reduce tumor size and prevent metastasis, limb-sparing removal, amputation