Childhood Cancer Flashcards

1
Q

Retinoblastoma

A

congenital malignant tumor, arises from embryonic retinal cells
if 1 child has it siblings probably do too

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2
Q

diagnosis of retinoblastoma

A
no red reflex
cats eye reflex is most common sign (think of what cat eyes look like when you shine a light in them)
strabismus- second most common sign
red, painful eye, often with glaucoma
blindness late sign
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3
Q

treatment of retinoblastoma

A

based on stage and time of dx
early- irradiation and cryotherapy to preserve vision in affected eye
bilateral disease- attempt to preserve useful vision in least affected eye
advanced tumor- enucleation
chemotherapy
chemotherapy- some controversy

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4
Q

prognosis of retinoblastoma

A

99% survival rate
tumor may spontaneously regress
concern with development of secondary tumors especially osteogenic sarcoma

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5
Q

complications of retinoblastoma

A

spread to brain and opposite eye
metastasis to lymph nodes, bone, bone marrow, and liver
secondary tumors, most often sarcomas, occurring in children who have been tx for retinoblastomas

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6
Q

post op care of retinoblastomas

A

large pressure dressing
dressing changes
sibling eye exams every 1-3 months for the first year

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7
Q

rhabdomyosarcoma

A

highly malignant cells in muscle, tendon, bursa, fascia and fibrous connective tissue, lymphatic, or vascular tissue

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8
Q

potential sites of rhabdomyosarcoma

A

head, neck, GU, extremities

symptoms may be vague and hard to dx

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9
Q

rhabdomyosarcoma treatment

A

highly malignant and frequent metastasis
complete removal of tumor if possible
radiation therapy for most
chemo to shrink may proceed with radiation
long term chemo 1-2 years

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10
Q

rhabdomyosarcoma prognosis

A

excellent in stage 1

poor if metastasis present during diagnosis

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11
Q

Hodgkins

A

more prevalent in 15-19 yo
neoplastic disease originating in lymphoid system
often metastasizes to spleen, liver, bone marrow, lungs and other tissues

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12
Q

how do you know its hodgkins?

A

presence of reed Sternberg cells

malignant B lymphocytes grow in lymph tissue

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13
Q

etiology of hodgkins

A

unknown but has been linked to Epstein Barr virus

need lymph node bx to diagnose

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14
Q

s/s of hodgkins

A

painless enlarged lymph nodes, fever, night sweats

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15
Q

treatment of hodgkins

A

radiation

chemotherapy alone or with radiation

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16
Q

prognosis of hodgkins

A

depends on stage, tumor bulk, classification

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17
Q

why should hodgkins kids not drink alcohol?

A

significant pain in effected nodes after consumption

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18
Q

complications for hodgkins

A

liver failure, secondary cancers, delayed puberty

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19
Q

can kids younger than 2 receive radiation?

A

no

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20
Q

signs and symptoms of brain tumors are

A

related to anatomic location, size, and child’s age

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21
Q

diagnostic testing to confirm a brain tumor

A
MRI
CT
EEG
LP
histologic diagnosis via surgery
22
Q

presenting symptoms of a brain tumor

A

headache, vomiting, clusiness, unsteady gate, blurred vision, head tilt, seizures, moor abnormality, weakness, behavioral or personality changes, FTT, irritability, vital sign disturbances

23
Q

Therapeutic management of brain tumors

A
depends on type of tumor
surgery
radiotherapy after the age of 2
chemo
prognosis
24
Q

postop care of brain tumors

A

positioning- tissue can shift in brain after tumor removal be mindful of this. child should remain midline, flat until they are able to sit. Children are usually sedated for a few days afterwards.
if child is sedated make sure eyes are hydrated
reduce ICP
neck flexion
NPO
comfort measures

25
neuroblastoma
most common malignant extracranial solid tumor of childhood and infancy develops in adrenal gland or retroperitoneal sympathetic chain (head, neck, chest, pelvis)
26
diagnosis of neuroblastoma
``` dx the younger the better radiology studies bone marrow IVP to determine renal involvement Metastasis may have already occurred before diagnoses ```
27
therapeutic management of neuroblastoma
clinical staging to establish treatment plan surgery to remove tumor and obtain bx radiation to shrink tumor for removal chemotherapy bone marrow transplant or stem cell rescue
28
Typical CBC of a leukemia kid
low RBC, HgB, Platelets High WBC Blasts high
29
consequences of leukemia
anemia from decreased RBC infection from neutropenia bleeding tendencies from decreased platelet count spleen, liver, and lymph glands show marked infiltration, enlargement and fibrosis
30
presenting symptoms of leukemia
``` fever pallor bleeding lethargy malaise anorexia large joint and bone pain ```
31
Cardinal signs of bone marrow failure
petechiae frank bleeding joint/bone pain fatigue
32
what does ANT stand for in leukemia
Anemia- low HgB neutropenia- risk of infections thrombocytopenia- bleeding
33
how do you confirm the diagnosis of leukemia
bone marrow bx | bone marrow will show immature cells
34
therapeutic management of leukemia
treatment for presenting symptoms combination chemotherapy cranial irradiation in some areas
35
Ewing sarcoma
malignant bone tumor arises from marrow especially in femur, tibia, ulna, humerus, vertebrae, pelvis, scapula, ribs, skull high malignancy rate
36
sign and symptoms of Ewing sarcoma
swelling and erythema at site. more likely o experience systemic symptoms (fever, spinal cord compression, respiratory distress)
37
treatment of ewing sarcoma
radiation commonly first approach | chemotherapy as adjunct to radiation
38
osteosarcoma
most frequent bone tumor in children peak age of incidence 15 years most primary tumor sites are in the metaphysis of long bones, especially legs can occur is distal femus, humerus, tibia, pelvis, jaw
39
signs and symptoms of osteosarcoma
pain limp decreased ROM
40
complications of osteosarcoma
metastasis to lungs or other bones | recurrence within 3 years
41
therapeutic management of osteosarcoma
traditional approach- radical surgical resection or amputation of affected area limb-salvage procedures- resection of bone with prosthetic replacement of affected area chemotherapy accompanying surgical treatment
42
nursing considerations for osteosarcoma
body image in adolescents support during concepts of amputation, surgical resection pain management phantom limb pain
43
nursing care of child with cancer
side effects of treatment managed treatment complications prevented child and family coping skills supports quality of life help child and family adjust to chronic illness growth and development maintained during treament
44
remission induced chemotherapy
rapid induction of complete remission, lasts 3-4 weeks, oral, steroids and IV chemotherapy
45
consolidation (CNS prophylaxis)
strengthen remission | introduce CNS prophylaxis, intrathecal and IV administration
46
intensification
destroy remaining or resistant cells
47
maintenance
prevent relapse, treat metastasis
48
signs of CNS involvement
``` headache persistent nausea or vomiting irritability dizziness seizures behavior and personality changes 6th cranial nerve palsy, abductus- lateral eye movement ```
49
what to know about chemo
it kills healthy cells too
50
short term side effects of chemo
``` immunosuppression infection myelosuppression nausea vomiting oral mucositis alopecia ```
51
long term side effects of chemo
microdonita and missing teeth hearing and vision changes hematopoietic immunologic or gonadal dysfunction endocrine dysfunction various alterations of the cardiorespiratory, GI, GU development of secondary cancer as an adolescent or adult