Disease of Infancy and Childhood 3 Tumors and Tumor-like Lesions Flashcards

1
Q

Tumors/tumor-like lesions

malignant tumor common children? but?

Two categories of tumor-like lesions distinguished from true tumors

A
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2
Q

Benign tumors and tumor-like lesions

4 we care about here?

most common neoplasm? children/adults?

A
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3
Q

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?

A
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4
Q

lymphatic tumor

lymphatic origin? while others? often occur where?

growth? can cause?

lymphangiectasis in contrst?

A
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5
Q

fibrous tumors

range?

apposed to adult ones?

gene?

A
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6
Q

Teratomas

what are they? can be what type of lesion?

most common teratoma of childhood?

peak in incidence?

malignant potential correlates with?

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7
Q

malignant tumors

main differences with childhood cancer?

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8
Q

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?

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9
Q

common malignant neoplasms by age

0-4 5-9 10-14

A
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10
Q

Neoblastic tumors

include what? (def)

most important member of this family? incidence?

mutations? familial?

high risk survival? prognosis better for who?

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11
Q

Neuroblastomas morph

arsie mainly where? size?

capsule? how does tissues look?

histo- cells?

background? rosettes?

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12
Q

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?

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13
Q

prognostic factors in neuroblastoma

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14
Q

neuroblastoma clin course prognostic features

under 2 present with? metastasize where?

paraspinal has?

skin?

produce what? diagnostic?

risks?

long term survival?

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15
Q

Neuroblastoma prognostic factors

stage- normal good prognosis? exception?

age- normal good? high risk?

morphology-

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16
Q

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?

A
17
Q

Neuroblastoma. other molecular variables

3

A
18
Q

neuroblastoma

2 experimental approaches to treatment

A
19
Q

wilms tumor

incidence? affects what part of body?

2 types? timing differ? treatment outlook?

A
20
Q

Wilms pathogen and genetics

risk of wilms increased with?

  1. first group has what syndrome? characterized by? incidence of wilms? chromo problem?

1st/2nd hit?

A
21
Q

wilms in congenital malformations

  1. what syndrome? this group has very high chance of wilms tumor.

disease characterized by? gene abnormal?

this gene and renal/gonads

A
22
Q

wilms congenital malformations

  1. 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?

A
23
Q

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?

A
24
Q

Wilms tumor morph

morphology? location?

micro-characterized by? 3 cell types?

stromal cells?

anaplasia? this correlates with?

A
25
Q

wilms tumor clin features

present with?

outlook?

adverse prognosis?

increased risk of?

causes of these risks?

A