Oncology Flashcards

Work in progress-cards soley from Nelson's (36 cards)

1
Q

Most common childhood cancers

A

leukemia or lymphoma

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2
Q

Peak incidence of embryonal tumors (neuroblastomas and retinoblastomas)

A

first 2 years of life

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3
Q

Peak incidence of ALL

A

2-5 yrs

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4
Q

Common symptoms for T-cell ALL and Non-Hodgkin Lymphoma

A

lymphadenopathy and organomegaly

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5
Q

General differences between malignant and infectious/inflammatory masses

A

malignant masses are firm, fixed, nontender. infectious/inflammory masses are softer, mobile, tender

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6
Q

Common metabolic emergency often seen in treatment of leukemia and lymphoma where large amounts of phosphate, potassium, and uric acid are released from lysed cells

A

tumor lysis syndrome

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7
Q

Define adjuvant therapy

A

chemotherapy administration after removal of the primary tumor

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8
Q

Protein kinase inhibitor that targets the effects of the t(9;22) translocation of chronic myeloid leukemia and acute lymphoblastic leukemia

A

Imatinib mesylate

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9
Q

Common extramedullary site for ALL

A

testes

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10
Q

Clinical presentation includes: older males (8-10), high WBC count, mediastinal masses, cervical lymphadenopathy, hepatosplenomegaly, CNS involvement

A

T-cell ALL

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11
Q

Characterized by immature blast cells, anemia, thrombocytopenia, and low/nml/high WBC count

A

acute leukemia

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12
Q

Why is treatment of AML different than ALL?

A

nonmyelosuppressive drugs are not effective for AML

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13
Q

Classification of low risk in ALL

A

1-9 yrs old, initial WBC count < 50,000, and favorable cytogenics t(12;21) translocation

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14
Q

Overall cure rate for childhood ALL and AML

A

ALL-80%. AML-50%

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15
Q

What do the following have in common: small noncleaved cell (Burkitt), lymphoblastic, and large cell?

A

histologic subtypes of NHL

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16
Q

Type of lymphoma that is diffuse, highly malignant, and shows little differentiation

17
Q

Most common clinical presentation of Hodgkin disease

A

painless, firm lymphadenopathy confined to one or two lymph node areas (usually supraclavicular and cervical)

18
Q

Type of lymphoma characterized by high fever, drenching night sweats, unintentional weight loss

A

Burkitt’s (B cell)

19
Q

Primary sites for lymphoblastic NHL (T cell)

A

mediastinum and cervical nodes

20
Q

Pathologic hallmark of Hodgkin disease

A

Reed-Sternberg cells

21
Q

Prognosis for Hodgkin disease and NHL

A

hodgkin-90% 5 yr survival. NHL-70-90% 3 yr survival

22
Q

Difference between brain tumors in children and adults

A

Children- primary tumors that originate in CNS. Adults- high grade astrocytomas or secondary tumors that are metastases from other carcinomas

23
Q

Most common solid tumors in children

24
Q

Symptoms of increased ICP

A

lethargy, HA, vomiting, inability to abduct the eye (CN VI palsy)

25
Examination technique of choice for CNS tumor
MRI
26
Administered immediately to reduce tumor associated edema
dexamethasone
27
5 yr overall survival rate for CNS tumors
50% due to high curability of cerebellar astrocytomas and medulloblastomas. Poor prognoses for gliomas and glioblastomas
28
Derived from the neural crest cells that form the adrenal medulla and the sympathetic nervous system
neuroblastoma
29
Most common presentation for neuroblastoma
abdominal pain or mass
30
Associated symptoms include: paraneoplastic syndromes-secretory diarrhea, profuse sweating, opsomyoclonus (dancing eyes and dancing feet), and periobital ecchymoses
neuroblastoma
31
Percentage of neuroblastomas that produce catecholamines that can be detected in the urine
90%
32
Prognosis for neuroblastomas
Patients under 1 yr have better prognosis than older patients
33
Most common malignant renal tumor of childhood
Wilms Tumor
34
Clinical presentation includes abdominal mass, abdominal pain, fever, HTN, hematuria
Wilms Tumor
35
Tx for Wilms tumor
nephrectomy followed by adjuvant chemo
36
Cure rate for patients with Wilms tumor
localized-85%. pulmonary metastases-70-80%