Disease of Infancy and Childhood 3 Tumors and Tumor-like Lesions Flashcards
Tumors/tumor-like lesions
malignant tumor common children? but?
Two categories of tumor-like lesions distinguished from true tumors

Benign tumors and tumor-like lesions
4 we care about here?
most common neoplasm? children/adults?

most common tumor of infancy?
type of hemangiomas encountered? located where? another term for flat large lesion? growth?
can be part of what disorder?
familial?

lymphatic tumor
lymphatic origin? while others? often occur where?
growth? can cause?
lymphangiectasis in contrst?

fibrous tumors
range?
apposed to adult ones?
gene?

Teratomas
what are they? can be what type of lesion?
most common teratoma of childhood?
peak in incidence?
malignant potential correlates with?

malignant tumors
main differences with childhood cancer?

incidence and types
most frequent arise in what system? compared to adults? under 10 increased incidence of what cancers?
most leathal?
histo- cells look like what? naming?
some ex?

common malignant neoplasms by age
0-4 5-9 10-14

Neoblastic tumors
include what? (def)
most important member of this family? incidence?
mutations? familial?
high risk survival? prognosis better for who?

Neuroblastomas morph
arsie mainly where? size?
capsule? how does tissues look?
histo- cells?
background? rosettes?

what is a ganglioneuroma?
type of cells you should see?
what do you see that is favorable?
spread to?
staging? what does each entail?
most present with?

prognostic factors in neuroblastoma


neuroblastoma clin course prognostic features
under 2 present with? metastasize where?
paraspinal has?
skin?
produce what? diagnostic?
risks?
long term survival?

Neuroblastoma prognostic factors
stage- normal good prognosis? exception?
age- normal good? high risk?
morphology-

neuroblastoma prognostic factors
what oncogene very important? chromo?
ploidy- important for what age? 2 types? better of two?
aggressive neuroblastoma is called? involves what damage?

Neuroblastoma. other molecular variables
3

neuroblastoma
2 experimental approaches to treatment

wilms tumor
incidence? affects what part of body?
2 types? timing differ? treatment outlook?

Wilms pathogen and genetics
risk of wilms increased with?
- first group has what syndrome? characterized by? incidence of wilms? chromo problem?
1st/2nd hit?

wilms in congenital malformations
- what syndrome? this group has very high chance of wilms tumor.
disease characterized by? gene abnormal?
this gene and renal/gonads

wilms congenital malformations
- distinct from other two. what syndrome? characterized by? what mechanism is happening? where? (what gene/location)
what gene/protein is activated? it is usually? other way it can be expressed?

wilms tumors
what is also important in wilms tumor? part of what pathway? works together with?
what is a nephrogenic rest? similar how? differ?
increased risk for?

Wilms tumor morph
morphology? location?
micro-characterized by? 3 cell types?
stromal cells?
anaplasia? this correlates with?

