Oncology- peds Flashcards
TNM staging
T= primary tumor TX= can't be measured T0= can't be found Tis= in situ T1-4= size and spread into structures
N= lymph nodes NX= can't be evaluated N0= no involvement N1-3= size, location, and/or number of lymph nodes affected
M= metastasis M0= no distant met M1= distant met
Acute lymphocytic leukemia (ALL)- epidemiology
2-5yr
Most common
Acute lymphocytic leukemia (ALL)- s/s
Lymphadenopathy Fever Hepatosplenomegaly (HSM) Fatigue Pallor Bruising/bleeding Bone pain/limp/tenderness Painless testicular enlargement Malaise
Acute lymphocytic leukemia (ALL)- dx
BMB/A >20%
Acute lymphocytic leukemia (ALL)- labs & imaging
CBC w diff and peripheral smear:
Anemia
Thrombocytopenia
Blasts
Acute lymphocytic leukemia (ALL)- tx
Chemo- determined by phenotyping
Acute lymphocytic leukemia (ALL)- prognosis
5 yr > 85%
CNS tumors- epidemiology
2nd most common
CNS tumors- s/s
HA Irritable N/V Macrocephaly Ataxia/impaired gait Impaired vision Seizure Papilledema Developmental delay
CNS tumors- dx
8x- histologic
CNS tumors- labs & imaging
MRI
CNS tumors- tx
Open surgical procedure - get biopsy and remove as much as possible
Avoid radiation <3yo
Chemo
Anticonvulsants - seizures
CNS tumors- prognosis
Depends on tumor type
5y >73%
Retinoblastoma- epidemiology
0-2yr
50% heritable - increased chance of passing to kids, and bilateral issues
Retinoblastoma- s/s
“Leukocoria
Strabismus, red inflamed eye, nystagmus”
Retinoblastoma- tx
REFER TO OPTHO
Get genetic testing
Cryotherapy Local/systemic Chemo Laser photocoagulation Enucleation Radiation
Retinoblastoma- prognosis
> 95%
if untreated- deadly
Osteosarcoma- epidemiology
Kids - sporadic
Radiation, chemo, genetics, Paget dx - bone breaks down and rebuilds weird
M>F
Osteosarcoma- s/s
Localized pain - last months
Soft tissue mass on exam - large, TTP
Osteosarcoma- dx
Biopsy
Osteosarcoma- labs & imaging
Xray:
- Destructive lesion
- Codman triangle - lesion lifts periosteum from bone
- Sunburst appearance
Osteosarcoma- tx
Chemo
Preop Chemo -> surgery -> postop chemo
RADIORESISTANT
Osteosarcoma- prognosis
Depends on tumor response to chemo
Ewing sarcoma- epidemiology
M>F
10-20yo
Ewing sarcoma- s/s
Bony pain or swelling- localized months
Limp, fracture
In LONG BONES AND PELVIS
Ewing sarcoma- dx
Biopsy
Ewing sarcoma- labs & imaging
Xray:
- Onion peel- periosteal reaction
CT/MRI:
- show extent of involvement
- Met w/u
Ewing sarcoma- tx
Chemo
Surgical resection + radiation
Ewing sarcoma- prognosis
5y: non-met- 55%
Met- 21%
Wilms tumor (Nephroblastoma)- epidemiology
Most common renal malignancy 2-5yo African WAGR syndrome Denys-Drash syndrome Beckwith-Weidemann syndrome
Wilms tumor (Nephroblastoma)- s/s
Abdominal mass or swelling- firm, smooth, nontender, unilateral mass
Abdominal pain, hematuria, fever, HTN
Wilms tumor (Nephroblastoma)- dx
Biopsy
Wilms tumor (Nephroblastoma)- labs & imaging
Abdominal u/s
Wilms tumor (Nephroblastoma)- tx
Surgical resection- all
Chemo- some
Radiation- based on stage/ histology