Pediatric Cancer Flashcards

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
Q

Identify risk factors for an osteosarcoma

A

growth spurt around 13-16yo,
recent injury,
Hx of radiation/chemo,
female

26
Q

s/s of osteosarcoma

A

localized pain lasting months,
soft tissue swelling,
limping,
pathological fracture

27
Q

Identify some long-term concerns with osteosarcoma.

A

reoccurrence, metastasis,
poor body image,
halted limb growth

28
Q

Identify labs for osteosarcoma.

A

elevated alkaline phosphate (byproduct of bone formation),
elevated ESR (indicating inflammation)

29
Q

Identify imaging for osteosarcoma.

A

X-ray showing woven bone matrix “sun burst” pattern,
CT, MRI,
bone scan

30
Q

Identify key treatment options for osteosarcoma.

A

chemo to reduce tumor size and prevent metastasis,
limb-sparing removal,
amputation