Chapter 8- Childhood Cancers Flashcards
(31 cards)
What are the most frequent childhood malignancy cancers?
- acute leukaemia
- brain tumours
- lymphoma
- neuroblastoma
When are neuroblastoma, nephroblastoma, retinoblastoma and medilloblastoma more common ? (age of incidence)
- First years of life
- they are congenital
Which cancer are more common in the teenage years?
bone malignancy,
hodgkins disease
testicular and ovarian
why is mortality and morbidity rates higher in children who recieved radiation and chemo?
- secondary malignancies
- developmental abnormalities related to administration
future complications
Most primary conditions associated with juvenile cancer have significant mortality in and of themselves. Such as?
neurofibromatosis, tuberous sclerosis von hippel-Lindau disease ataxia telangiectasia Down syndrome
Which children are at the highest risk of serious late effects from their cancer treatment, including second cancers, congestive heart failure, and eventual joint replacements?
Those treated for:
Brain tumours
hodgkinds lymphoma,
or any use of radiation to the abdomen, pelvis or chest.
what tumors is the most common childhood solid tumor, and also the second most frequent malignancy in children and adolescents?
brain tumours
- 45% mortality rate from the disease and highest morbidity
- sxs: headaches, vomiting, papilledema, seizures, personality changes, balance and weakness.
- usually diagnosed late
What is the most common juvenile brain lesion?
Astrocytoma
- low-grade malignancies more favourable.
- tx is radiation, chemo and surgery.
- 90% survival
which astrocytomas have a more favourable prognosis
Low-grade (grade 1 and 2) with complete excision.
What is the most lethal type of astrocytomas?
Glioblastoma (multiform)
What is a Medulloblastoma?
occurs exclusively in children
- in posterior fossa of the brain
- complete remove is difficult and usually requires re-excision
- 5 year survival rate of 70%
What is the Ependymoma
posterior fossa tumor
- poor prognosis
- tx’ed with radiation,
- 40% 5 year survival rate
What is a neuroblastoma?
most common solid extra-cranial tumour in children.
- arise in abdomen (adrenal gland or sympathetic ganglia)
- sxs: bone pain, loss of appetite, weight loss, fatigue≥ Anemia, high platelet and iron counts
- CXR diagnosis, f/u MRI or CT.
- tx: chemo and bone marrow transplant, and radiation. Surgery is not always effective.
- stage 3 and 4 have poor prognosis
- mortality can be sig for 10 years
What is Nephroblastioma ( Wilms’ tumour)
- second most common abdo tumour in children
- starts in kidney and is composed of blastema, epithelia and stroma
- 7% Bilateral.
- sporadic + genetic cases
- sxs: asymptomatic mass or swelling, sometime fever or hematuria, HTN
- U/s or CT diagnosis.
- metastasis is common.
- tx: surgery and chemo. post-op radiation if needed
What is the survival rate for Wilms’ tumour?
better for stage 1 and 2
5 year survival 90%, unless cells show aggressive behaviour.
- 150% mortality 5-10 years. Better prognosis as kids get older.
- morbidity ^^ d/t radiation = muscle atrophy, bone grow issues, spinal shortening.
What are retinoblastomas?
higher rates of cure 90%
cancer is bilateral
dx before 5 yo.
usually familial, 25-30% of dx are d/t mutation in gene RNA
-older age is worst prognosis d/t advancement of disease
- sxs: leukocoria, white papillary reflex of light during
- dx: opthomology exam, ultrasound and bone scans
How are retinoblastoma’s treated?
- used to remove whole eye. only now used when 50% of retina is involved with tumour.
- Main tx is radiation, and chemo if child is at risk of metastasis.
True or False
those who has the familial type have a significant risk of developing a second cancer?
yes,
develop in and outside of radiation field.
most common second cancer are soft tissue sarcomas, and ostosarcoma.
What are the two most common types of malignant bone tumors in children?
osteosarcoma (60) and Ewing sarcoma.
- later occurring cancer (10’s/20’s)
what are some growth changes that occur with osteosarcoma?
- usually correlate with growth spurts
- children with dx are taller than peers
- appears in bones with greater increase in size/length ie: distal femur
What are the symptoms, and treatments for osteosarcoma?
sxs: pain and swelling,
dx: Xray, and bone marrow/CBC tests. MRI assess the severity.
complication: pulmonary metastases,
tx: chemo, amputation.
What is Ewing Sarcoma?
less common, Males > females
- dx made on biopsy,
- sxs: pain swelling and bone mass on Xray signs and diagnostic
- better prognosis, unless metastatic
What are Rhadomyosarcoma?
most common pediatric sarcoma,
- occur everywhere in the body
- prognosis is related to age of the child, site or origine, metastasis and lymph node involement.
what are the symptoms of rhabdomyosarcomas?
palpable mass,
organ displament d/t tumour
- sxs relate to location of tumour
- hard to diagnose, biopsy and histrochemical staining is most effective diagnostic test.