Oncology Flashcards
Most common malignant neoplasm in chilhood
Leukemia
Most common malignant childhood malignancy
2-6y/o; M>F
Clinical manifestation:
Acute onset <4 weeks
Acute lymphobastic leukemia
Diagnosis of ALL
BMA: >25% of the BM cells as a homogenous population of lymphoblasts
Poor prognostic factors
<2y/o or >10y/o Male WBC >100,000u/L on presentation Presence of CNS leukemia Presence of Mediastinal Mass
Single most important prognostic factor in ALL
Treatment
Treatment of ALL
Remission induction: to eradicate leukemic cells
Condolidation phase: 14-28wks to prevent CNS relapse
Maintenance phase: 2-3years
Drugs used in Remission induction
Vincristine, Prednisone, L-asparaginase for 4 weeks PLUS CNS prophylactic irradiation or chemotherapy
Drugs used in Maintenance Phase
Mercaptopurine daily AND Methotrexate weekly
Complication pf treatment of ALL
Tumor lysis syndrome
Remission in ALL
<5% blasts in the BM and a return of neutrophil and platelet count to near-normal levels after 4-5weeks of treatment
Sites of Relapse in ALL
Bone marrow
CNS
testes
Where does ALL spread?
Liver
Spleen
Lymph nodes
Bimodal age distribution: 20-30 years and >50y/o
REGIONAL Painless nontender, firm, rubbery cervical or supraclavicular adenopathy
Hepatosplenomegaly is Rare; contiguous lymph mode spread
Weight loss >10% over 3mos, unexplained high grade fever, drenching night sweats
Reed-Sternberg Cell
Hodgkin’s lymphoma
60% of all lymphomas in children and adolescents
Systemic adenopathy; Hepatosplenomegaly; more extranodal involvement; non-contiguous lymph node spread
Weight loss >10% over 3mos, unexplained high grade fever, drenching night sweats
Non-Hodgkin’s Lymphoma
Most common posterior fossa tumor of childhood; has the best prognosis
Clinical Manifestations: personality changes, signs of increased ICP, motor weakness, ataxia, seizures
Dx: MRI
Tx: resection, radiotherapy, steroids, supportive
Cerebellar Astrocytoma