Pediatrics/Oncology Flashcards

1
Q

MCCs of death in children older than 1

A
  1. injuries

2. cancer

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2
Q

most common type of pediatric malignancy

A
  1. leukemia
  2. brain tumors
  3. lymphomas
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3
Q

more prevalent malignancies:
Newborn
infancy and childhood
adolescence

A

Newborns: neuroblastoma, other embryonal tumors(wilm’s)

infancy: leukemia, neuroblastoma, wilm’s, retinoblastoma
adolescence: lymphoma, gonadal tumors, bone tumors

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4
Q

prevalency of leukemias

A

ALL>AML>CML

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5
Q

HTLV association with leukemia

A

T-cell leukemia

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6
Q

prognosis of ALL & AML

A

ALL>AML

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7
Q

EBV associated lymphoma

A

African Burkitt’s lymphoma

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8
Q

what is the difference between children and adult non-hodgkin lymphoma?

A

rapidly growing tumor with distant metastases in children

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9
Q

hodgkin or non hodgkin patients are older

A

hodgkin lymphoma

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10
Q

most common brain tumor in children

A

cerebellar astrocytoma

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11
Q

common location for brain tumors

A

60% infratentorial

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12
Q

clinical presentation of infratentorial tumors

A
increased ICP, 
vomiting.
morning headache, 
increased HC
CN 6 palsy
UWG
ataxia
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13
Q

clinical presentation of supratentorial tumors

A

focal deficit
seizure
long tract sign
visual field defect

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14
Q

most common primary renal neoplasm of childhood

A

Wilms tumor (nephroblastoma)

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15
Q

both kidney in wilms

A

5-10%

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16
Q

DDx for Wilms

A

hydronephrosis
polycystic kidney dis.
RCC
neuroblastoma

17
Q

Clinical presentation of Wilms

A

80% asymptomatic: unilateral abdominal mass
HTN, hematuria, abd. pain, vomitting
respiratory symptoms

18
Q

metastasis of wilms

A

may have pulmonary metastasis at time of primary Dx

19
Q

associated congenital abnormalities with wilms

A

WAGR syn.
Beckwith-Wiedemann syn.
Denys-Drash syn.

20
Q

prognosis of wilms

A

90% longterm survival

21
Q

Rx of wilms

A

nephrectomy

staging and chemo;radiation for higher stage

22
Q

most common cancer in 1st year of life

A

neuroblastoma

23
Q

most common site for neuroblastoma

A

adrenal medulla

24
Q

neuroblastoma at presentation time

A

metastases are common,>50% present with advanced stage dis.

25
Q

metastases of neuroblastoma

A

usually to bone or bone marrow

26
Q

periorbital ecchymoses, abd. pain, emesis, fever, weight loss, anorexia, hepatomegaly, blueberry muffin skin nodule

A

neuroblastoma

27
Q

neuroblastoma paraneoplastic Sx

A
HTN
Palpitation
sweating
diarrhea
FTT
opsomyoclonus
28
Q

diagnostic criteria for neuroblastoma

A
  • unequivocal histologic Dx from tumor Bx
  • evidence of metastases to bone marrow (‘rosettes”) on aspirate analysis, with concomitant elevation of urine or serum catecholamine metabolite (VMA,HVA)
29
Q

staging for neuroblastoma

A

CT or MRI of chest, abd., pelvis, bone scan, MIBG scan

30
Q

good prognostic factors for neuroblastoma

A
age and stage
<1y
I,II,IV-S
primary site: post. mediastinum
low serum ferritin
specific histology
tumor cell markers(aneuploidy, absent M-myc)
31
Q

prognosis of neuroblastoma

A

poor

32
Q

common extracranial solid tumors

A

neuroblastoma
wilms
rhabdmyosarcoma

33
Q

common sites for rhabdomyosarcoma

A

H&N
GU
Ext.

34
Q

presentation of rhabdomyosarcoma

A

firm, painless mass

35
Q

metastases of rhabdomyosarcoma

A

lung, bone, bone marrow

36
Q

generalized LAD

A
CBC diff, B/C
Uric acid, LDH
ANA, RF, ESR
EBV, CMV, HIV serology
toxoplasma titre
fungal serology
CXR
PPD
biopsy
37
Q

regional LAD

A

period of observation in an asymptomatic child
trial of oral antiobiotics
ultrasound
biopsy (especially if persistent>6w and/or B symptoms)