Low Priority: Lymphoma, TBI, Sarcoma, Skin, Pediatrics

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Last updated 5:26 AM on 9/12/26
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65 Terms

1
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What is the hallmark cell of Hodgkin’s Lymphoma

Reed-Sternberg cells

2
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What is the hallmark cell of Hodgkin’s Lymphoma?

20–34 (bi-modal peak, second peak in elderly and tend to do worse)

3
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What are the risk factors for Hodgkin’s?

EBV (Epstein-Barr virus),

immunosuppressive drugs

4
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What are B-symptoms?

Night sweats, fever, weight loss

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What are A-symptoms?

Asymptomatic (no symptoms)

6
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What chemo regimen is used for Hodgkin’s?

ABVD (2–3 cycles) for standard risk; BEACOPP for high risk

7
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What RT doses are used for Hodgkin’s?

20–30 Gy (early stage); 30–40 Gy

(bulky disease)

8
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What technique has replaced the mantle field for Hodgkin’s?

ISRT —

Involved Site Radiation Therapy

9
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What is the classic RT technique for Hodgkin’s involving lower abdomen?

Inverted-Y field; paraaortic field

10
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What age group gets NHL and what causes it?

Age 50; caused by lifetime

accumulation of DNA mutations

11
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What chemo is used for NHL?

R-CHOP (primary); RT adjuvant if not

responsive

12
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What are the RT doses for NHL?

Localized: 24–30 Gy; Aggressive: 30–36

Gy

13
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What is the clinical presentation for Hodgkins

Painless mass (around s’clav, cervical, medistinal), enlarged lymph nodes

14
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What is the staging system for lymphoma and what characterizes the stages?

Ann Arbor Staging
1 → Single LN region
2 → 2+ LN on same side of diaphragm
3 → LN on both sides
4 → Extranodal involvement (bone marrow, liver, etc)

15
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What is ALL and who gets it?

Acute Lymphoblastic Leukemia — most

common cancer in children; bone marrow origin, spreads to blood, LN, liver, spleen,

CNS

16
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What chromosome abnormality is associated with ALL?

Philadelphia

chromosome — translocation between chromosomes 9 and 22 (BCR-ABL)

17
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When is RT used in ALL?

Only for CNS or spinal spread

18
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What are the risk factors for AML?

Smoking, prior ionizing radiation

19
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What chemo is used for AML?

Cytarabine + daunorubicin (“7+3” regimen)

20
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What is the RT role in AML?

Palliative or pre-bone marrow transplant

conditioning

21
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What is the risk factor for CLL?

Agent Orange exposure; age 70

22
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What is the genetic hallmark of CML?

BCR-ABL gene fusion → treated

with TKIs (tyrosine kinase inhibitors)

23
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What does CRAB stand for in multiple myeloma?

Calcium

(hypercalcemia), Renal failure, Anemia, Bone lesions

24
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What is the TBI dose and fractionation?

12 Gy / 6 fractions — 2 fractions

per day × 3 days

25
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What is the lung dose limit for TBI?

<7 Gy (achieved with lung blocks)

26
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What is the setup used for TBI?

Extended SSD

27
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What is the purpose of TBI?

Conditioning (myeloablative) before bone

marrow/stem cell transplant — destroys existing marrow and immunosuppresses

28
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What is the tissue of origin for soft tissue sarcomas?

Mesenchymal tissue

29
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Where are soft tissue sarcomas most commonly located?

Extremities

30
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What are the two most common soft tissue sarcoma types?

Liposarcoma

and leiomyosarcoma

31
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What is used for staging of soft tissue sarcomas?

Grade (differentiated vs highly undifferentiated) (not just

TNM)

32
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What are the RT doses for soft tissue sarcoma?

Pre-op: 50 Gy / 25 fx

&gt; - Adjuvant (post-op): 60–66 Gy / 33 fx &gt; - Advanced: 70 Gy / 35 fx

33
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What is the most common primary malignant bone tumour?

Osteosarcoma

34
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What age group gets osteosarcoma?

24 years OR 60+ (associated with

rapid bone growth in young;

35
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What is the treatment for osteosarcoma?

Surgery (amputation or limb-

sparing) + chemo (cisplatin + doxorubicin); RT = SBRT 50–60 Gy / 3–5 fx

36
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Differentiate pre/post op sarcoma RT characteristics

Pre-op = small field + better cell kill, worse healing (RT impairs healing)

Post-op = large field + more fibrosis, better heal

37
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What genetic conditions predispose to skin cancer?

Xeroderma

pigmentosum, albinism

38
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What are the subtypes of BCC and their appearance?

-Nodular/pearly/rodent ulcer
- Superficial/scaly
- Morphea/flat ill-defined

39
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How do BCC and SCC differ in growth rate?

BCC = slow growing; SCC =

fast growing

40
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What does ABCDE stand for in melanoma?

Asymmetry, Border irregularity, Color variation, Diameter >6mm, Evolve

41
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What is the primary treatment for skin cancer? When is RT used?

Surgery = primary; RT = adjuvant

42
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What RT doses are used for skin cancer?

35 Gy/7fx | 45 Gy/10fx | 50

Gy/20fx

43
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What is the role of RT in melanoma?

Mainly palliative (melanoma is

relatively radioresistant)

44
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Electron Beam for Skin — Depth Rule

Energy (MeV) ≈ depth (cm) × 3 OR: depth of treatment ≈ beam energy ÷ 3 (the “1/3 rule”)

45
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What dose of radiation to the thyroid is a risk factor for thyroid cancer?

1 Gy to the thyroid (specifically papillary subtype)

46
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What hormones does the thyroid produce?

T3 and T4

47
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What is Graves disease?

Autoimmune hyperthyroidism — weight loss,

exophthalmos, elevated metabolic rate

48
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What are the four types of thyroid cancer in order of frequency?

Papillary (most common) → Follicular → Medullary → Anaplastic

49
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How is thyroid cancer treated? What is the RT dose?

I-131 (radioactive iodine) for imaging and treatment; EBRT if unresectable: 5000–7000 cGy

50
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What is the primary tumour of the pituitary gland and where is it located?

Benign adenoma in the sella turcica

51
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What are the symptoms of a pituitary adenoma?

Headache + visual field

defects (compression of optic chiasm)

52
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When is RT used for pituitary adenoma?

If not resectable or near visual

structures → SBRT or proton therapy

53
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What is the second most common cancer in children?

Brain tumours

54
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What are the four types of pediatric brain tumours?

Astrocytoma,

ependymoma, medulloblastoma, brainstem glioma

55
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Why is proton therapy preferred for pediatric brain tumours?

Reduced

exit dose → less damage to developing brain tissue and growth structures

56
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What are the CSI doses for medulloblastoma?

- Standard risk: 23.4 Gy
- High risk: 36 Gy
- Posterior fossa boost: 54–55.8 Gy

57
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What is leukocoria and which cancer causes it?

“Cat’s eye reflex” —

caused by retinoblastoma (most common intraocular tumour in children)

58
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How is retinoblastoma treated with RT?

I-125 brachytherapy: 3000–4000

cGy over 1 week; daily general anesthesia

59
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What is the most common extracranial solid tumour in children?

Neuroblastoma (3rd most common cancer overall in children)

60
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What is the median age for neuroblastoma?

<17 months; usually located

in the abdomen

61
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What is the high-risk neuroblastoma treatment sequence?

Induction

chemo → Surgery → Myeloablative chemo → SCT → RT → Immunotherapy

62
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What is Wilms tumour and how is it treated?

Kidney cancer

(nephroblastoma), age 3–4, clear cell type, can be bilateral. Nephrectomy → Stage 1–2:

chemo; Stage 3–4: chemo + RT (1080–2000 cGy)

63
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What is Ewing’s sarcoma treatment?

VDC/IE chemo; surgery preferred 12

weeks after chemo; if no surgery: 45 Gy → boost to 55.8 Gy; whole lung RT = 15 Gy

64
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What staging system is used for pediatric NHL?

St. Jude’s staging

system

65
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