oncology Flashcards

(33 cards)

1
Q

define neuroblastoma

A

Most common malignancy. Tumors arise during fetal or early postnatal life from sympathetic nerve cells.

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2
Q

where are neuroblastomas found

A

o Adrenal medulla
oabdominal sympathetic ganglia
o Cervical, thoracic ganglia

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3
Q

signs and symptoms of neuroblastoma

A
Abdominal:
Mass 
pain
Respiratory:
RDS
Dysphagia
spinal cord compression:
Altered defecation, urination 
Gait
Neck/thorax:
Horner's 
Excess catecholamine secretion:
Diarrhea, weight loss, hypertension
Metastatic:
Bone pain
Anemia
Raccoon eyes 
Opoclonus myoclonus ( dancing eyes dancing feet)
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4
Q

laboratory diagnosis of neuroblastoma

A

High levels:
LDH
Ferritin
catecholamine metabolites ( urine)

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5
Q

imaging in neuroblastoma

A

Xray
US
CT
MRI

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6
Q

other investigations neuroblastoma

A

biopsy- bone marrow, skin,excisional) see small round blue cells
MYCN amplification

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7
Q

Define stage 4s neuroblastoma

A

Localized primary tumor dissemination limited to skin, liver, and bone marrow
only for <1 year old. Undergoes spontaneous regression even without treatment

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8
Q

Treatment of neuroblastoma

low risk

A

usually low risk diseased so adjuvant chemotherapy and radiotherapy not needed
Only need surgical resection

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9
Q

Treatment of patient intermediate risk neuroblastoma

A

chemotherapy
radiotherapy ( if unresectable tumour)
resection

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10
Q

Treatment of patient high risk neuroblastoma

A

chemotherapy
stem cell transplant
retinoic acid
immunotherapy

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11
Q

define wilm’s tumour

A

The most common cancer of the kidneys in children

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12
Q

What is wilm’s tumour associated with

A

o Hemihypertrophy
o WAGR complex: Wilms tumor,
Aniridia (absence of the iris), Genitourinary malformations, Range of developmental delays (WT1 deletion)

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13
Q

Clinical presentation of wilms tumour

A
Palpable abdominal/flank mass ( usually painless)
hematuria
hypertension
fever
US,CT,MRI
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14
Q

Treatment of wilms tumour

A

Resection
Chemotherapy
Radiotherapy

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15
Q

Define teratoma

A

malignant, aggressive tumors that form from multiple tissues foreign to the organ they come from

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16
Q

location of teratoma

A

saccrococcygeal
gonads
thoracoabdominal

17
Q

diagnosis of teratoma

A

Disorganized heterogeneous appearance on ultrasound with solid, cystic, or complex components.
AFP

18
Q

define sacrococcygeal teratoma

A

Tumour that grows on the base of the coccyx

19
Q

Classification of sacrococcygeal teratoma

A

oPredominantly solid & vascular
oPredominantly cystic with relatively little vascularity
o Mixed with equal amounts of solid & cystic structures.

20
Q

Signs and symptoms of sacrococcygeal teratoma

A

Sacrococcygeal teratomas can grow rapidly in the fetus and require very high blood flow resulting in fetal heart failure, a condition known as hydrops.
signs:
dilation of heart, pleural , pericardial effusion, polyhydramnios

21
Q

treatment of sacrococcygeal teratoma

A

complete excision ( risk of malignancy)

22
Q

define cervical teratoma

A

tumour in the neck partly solid partly liquid

23
Q

Clinical presentation of cervical teratoma

A

Tracheal & esophageal obstruction can lead to acute respiratory failure in the newborn, or prenatal polyhydramnios

24
Q

Diagnosis of cervical teratoma

A
Prenatal
US- polyhydramnios
Postnatal:
Xray, Ultrasound,CT,MRI
AFP,HCG,urinary catecholamines
25
Define vascular tumour
True neoplasms due to cellular hyperplasia
26
Define vascular malformation
Congenital legions due to errors during embryonic development, have normal endothelial cell division.
27
define hemangioma
benign tumor of the vessels appears on the skin.
28
Clinical features of hemangioma
``` skin lesions ( mostly in head and neck)- early sign superficial lesions- red, raised lesion, may cause ulceration with bleeding Subcutaneous lesion- raised and blue in colour ```
29
Complication of hemangioma
``` Ulceration,bleeding,pain Airway obstruction Liver hemangioma- CHF Facial lesions in eyelid, lip etc ambylopia- brain fails process inputs from one eye, favours the other eye ```
30
Diagnosis of hemangioma
US,MRI
31
Treatment of hemangioma
``` observation for majority ( will regress) If has complications: Corticosteroids( stops angiogenesis) propranolol (vasoconstriction) sclerosing agent injection Resection ( if well localised) ```
32
vascular malformations presentation
Present at birth as permanent flat, pink red cutaneous lesions that do not fade with time
33
Treatment of vascular malformations
mainly for cosmetic purposes: Laser therapy Surgery sclerotherapy