T3 - Non-Hodgkins Lymphoma, Aplastic Anemia, Retinoblastoma Flashcards

1
Q

Non-Hodgkins Lymphoma derives from which type of cells?

A

Mature B Cells

T Cellls

Cells of uncertain lineage

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2
Q

What are the three most common malignancies in children?

A

Acute Leukemia

Brain Tumor

Non-Hodgkins Lymphoma

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3
Q

What are the most common sites for NHL?

A

Abdomen

Mediastinum

Head/Neck

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4
Q

What s/s of NHL in abdomen?

A

pain

distention

n/v

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5
Q

S/S of NHL in Mediastinum?

A

pleural effusion

pain

dyspnea

dysphagia

SVC syndome (sweating of upper arm, face, and neck)

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6
Q

S/S of NHL in Head/Neck

A

painless, non-tender mass

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7
Q

Which treatment is used the most w/ NHL?

A

Chemo

  • occasionally radiation if tumor interferes w/ vital structures
  • occasionally surgery where debulking is beneficial
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8
Q

What is the most important factor in determining prognosis of NHL?

A

extent of disease at Dx is determined by pretreatment staging

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9
Q

Clinical manifestations of NHL

A

Lymph node involvement in limitation to 1 or 2 adjacent lymphatic regions

Extra nodal site, nasopharynx, oropharynx, or other isolated extra nodular sites with or without lymphadenopathy

GI involvement limited to mesentery

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10
Q

— is a tumor of the eye.

A

Retinoblastoma

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11
Q

80% of Retinoblastomas are diagnosed at what age?

A

before age 5

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12
Q

What is noteworthy about the genetics of Retinoblastoma?

A

gene is present in all body cells in inherited from but only tumor cells in non-inherited form

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13
Q

S/S of Retinoblastoma

A

FTT

Strabismus

Glaucoma

Orbital Cellulitis

Blood Shot Eyes

Nystagmus

Leucocoria (white discoloration of pupil)

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14
Q

What does fundus examination reveal?

A

allows visualization of the entire retina in both eyes to determine extent of tumor

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15
Q

What is the most important factor in the prognosis for visual acuity w/ Retinoblastoma?

A

early diagnosis

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16
Q

Treatments for Retinoblastoma

A

Enucleation

Radiation

Cryotherapy

Photo-coagulation

Chemo

17
Q

What is the most common second malignancy w/ Retinoblastoma?

A

osteosarcoma

18
Q

How many types of Aplastic Anemia?

A

Two

  • Congenital
  • Acquired
19
Q

Fanconi’s Anemia is —

A

congenital

20
Q

What are the S/S of Congenital Aplastic Anemia

A

Pallor

Purpura (due to thrombocytopenia)

Infection (due to leukopenia)

21
Q

What are the S/S of Acquired Aplastic Anemia?

A

Pallor

Weakness

Loss of appetite

22
Q

Possible causes of Acquired Anemia

A

Drugs

Chemicals

Toxins

Irradiation

Infections (hepatitis, AIDS, Rocky Mountain SF)

23
Q

Lab values to identify Aplastic Anemia

A

decreased hematopoeietc cells w/ replacement by fatty tissue

anemia

thrombocytopenia

bone marrow

24
Q

Treatment for Congenital Aplastic Anemia

A

Supportive w/ packed cell transfusions of platelets and WBCs on occasion

Steroid/Androgen therapy

Bone marrow transplant

25
Q

Treatment for Acquired Aplastic Anemia

A

Remove exposure to hazardous drugs/toxins

Avoid bleeding into vital organ (platelet transfusions)

Oral contraceptives to suppress menses in females

Avoid aspirin

Avoid infections and treat promptly

Bone marrow transplant

Drugs

  • prednisone
  • oral androgens
  • cyclosporine