Burkitts Lymphoma Flashcards

1
Q

What are the to main types of lymphoma?

A

Non-hodgkins and Hodgkins

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2
Q

What is the commonest childhood cancer in tropical Africa?

A

Non-Hodgkins Lymphoma

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3
Q

What is the malignant solid tumor of B or T cell lymphocytes?

A

Non-Hodgkins lymphoma

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4
Q

Age range for non-hodgkins and peak age

A

4-9 years, peak 5 years

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5
Q

Rare age ranges for Non-Hodgkins lymphoma

A

<2years and >16years

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6
Q

Gender ratio of Non-hodgkins lymphoma?

A

Males:females
2:1

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7
Q

Favourable prognosis for NHL?

A

Minimal therapy in early stages

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8
Q

General symptoms for NHL?

A

No. Depends on location of tumor

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9
Q

Clinical presentation of NHL in the head and neck.

A
  1. Neck or jaw mass involving nasopharynx, sinuses-painless or painful
  2. Proptosis
  3. Dental anarchy
  4. Breathing or swallowing difficulty
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10
Q

Clinical presentation of NHL in the abdomen

A
  1. Abdominal mass +/- ascites
  2. Abdominal pain
  3. Nausea and vomiting, constipation +/- bowel obstruction
  4. Urinary retention
  5. Spinal cord compression- paraplegia
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11
Q

Clinical presentation of a T cell lymphoblastic lymphoma

A
  1. Cough, stridor, dyspnea +/- pleural effusion +/- SVC obstruction
  2. Hepatosplenomegaly
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12
Q

Features of Endemic type?

A

5-10 years
Male>female
Common in Africa, Brazil and Turkey
Jaw, abdomen, CNS, CSF
95% - Epstein Barr Virus
Rapidly growing tumor of the jaws or abdomen in high risk groups with doubling time of 24 hours.
Short duration of PC.

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13
Q

Features of Sporadic type

A

6-12 years
Male>female
Abdomen, bone marrow, lymph nodes, ovaries.

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14
Q

Diagnosis of endemic type

A

Biopsy for histology
😻 starry sky appearance

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15
Q

What are the sanctuary sites for Burkitts lymphoma?

A

Indication of poor prognosis
Testes
Breasts
Thyroid gland
Pancreas
Skin
Epidural space
Bone

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16
Q

What hematologic investigations will you do and what do you expect?

A

Full Blood Count - to rule out leukemia
Blood film comment
Renal and Liver Function tests
LDH( lactic acid dehydrogenase) - raised in Non-Hodgkins lymphoma
Uric acid- increased in high tumor burden
HIV test

17
Q

What imaging investigations will I do?

A

Chest X-ray for mediastinal mass
Abdominal and /or neck ultrasound
CT scan / MRI
Echocardiogram- ejection fraction of doxorubicin administration.
Needle biopsy
Pleural or ascites fluid
Bone marrow aspirates + trephine for staging
Lumbar puncture- CNS status
Immunohistochemistry

18
Q

What is stage A?

A

Single extrabdominal tumor site

19
Q

Stage B?

A

Multiple extra abdominal site

20
Q

Stage AR?

A

Completely (>90%) resected intraabdominal tumor.

21
Q

Stage C?

A

Intraabdominal tumor without involvement of other sites

22
Q

Stage D?

A

Intraabdominal and Extra abdominal tumor sites

23
Q

Treatment
Cycle 1/Prephase

A

Oral medications with Cyclophosphamide, Prednisolone and Allupurinol

24
Q

Alternate treatment cycle

A

Vincristine, Doxorubicin, Cyclophosphamide, prednisolone.
Intrathecal with
Cytarabine, vincristine, cyclophosphamide, prednisolone-

25
Q

Treatment regimen

A

Each cycle for 3 weeks after 3 weeks of no drugs.
Minimum of 6 cycles and maximum of 10 cycles

26
Q

Prognostic factors

A

Tumor burden is unfavorable if it’s high
Bone marrow involvement
CNS involvement
Presentation above 13 years
Relapse shortly after remission( 3 months) has poor prognosis