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
metastases of neuroblastoma
usually to bone or bone marrow
26
periorbital ecchymoses, abd. pain, emesis, fever, weight loss, anorexia, hepatomegaly, blueberry muffin skin nodule
neuroblastoma
27
neuroblastoma paraneoplastic Sx
``` HTN Palpitation sweating diarrhea FTT opsomyoclonus ```
28
diagnostic criteria for neuroblastoma
- 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
staging for neuroblastoma
CT or MRI of chest, abd., pelvis, bone scan, MIBG scan
30
good prognostic factors for neuroblastoma
``` 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
prognosis of neuroblastoma
poor
32
common extracranial solid tumors
neuroblastoma wilms rhabdmyosarcoma
33
common sites for rhabdomyosarcoma
H&N GU Ext.
34
presentation of rhabdomyosarcoma
firm, painless mass
35
metastases of rhabdomyosarcoma
lung, bone, bone marrow
36
generalized LAD
``` CBC diff, B/C Uric acid, LDH ANA, RF, ESR EBV, CMV, HIV serology toxoplasma titre fungal serology CXR PPD biopsy ```
37
regional LAD
period of observation in an asymptomatic child trial of oral antiobiotics ultrasound biopsy (especially if persistent>6w and/or B symptoms)