The Child with Cancer Flashcards

1
Q

Leukemia Acute Lymphocytic Leukemia (ALL)

A
  • Leukemia is the unrestricted proliferation of immature white blood cells and is the most common type of childhood cancer (lymphoblasts)
  • 2-5 cases per 100,000 children
  • Peak onset is between 2 and 3 years of age
  • Up to 90% survival rate
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2
Q

Leukemia Acute Lymphocytic Leukemia (ALL)
S/S

A

***Petechiae, Fever, Fatigue

Decreased RBC= anemia
- tired, fatique, pallor, headache, SOB, lethargy, hypoxia
Decreased normal wbc = infection
- fever that won’t go away with meds/ cooling measures, high WBC/ low neutrophil (neutropenia) , don’t have white discharge
Decreased Platelet= Hemorrhage
- decreased amount of PLT: bruising/ epistaxis/ blood in stool or urine/ petechiae
Increased pressure = bone and joint pain/ thinning and weakening of bone
- pathologic faracture: bone breaks from inside outward
Extra medullary infiltration= enlarged spleen, liver, lymph nodes
- Splenomegaly, hepatomegaly, lymphadenopathy
Increased metabolism= starvation of cells, hypoglycemia
Meningitis
-
- Minor infection, such as a cold, fails to completely disappear
- Continues to be pale, listless, irritable, febrile, and anorexic
- Most frequent signs & symptoms are result of infiltration of bone marrow
- Fever, pallor, fatigue, anorexia
- Hemorrhage (usually petechiae), bone and joint pain
- With neutropenia body’s normal bacterial flora can become aggressive pathogens
- Vague abdominal pain
- ***Petechiae, Fever, Fatigue

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3
Q

Leukemia Acute Lymphocytic Leukemia (ALL)
Nursing intervention:

A
  • anemia: Iron, PRBC transfusion, O2, monitor Hct/ Hgb, administer EpiGen: given once lukoblasts are under control
  • Infection: neutropenia isolation/ reverse (pressurized) isolation: wear everything except google
    — No live plants, no fresh fruits and veggies, no yogurt, no unpasteurized meat/ dairy,
    — monitor WBC (CBC w/ dif), absolute neutrophil count (ANC): 500 or < : severely neutropenic/ 1500 or >: safe
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4
Q

Leukemia Acute Lymphocytic Leukemia (ALL)
Pathologic and Related Clinical Manifestations

A

Tumor Lysis Syndrome (hyperuricemia,
When you use radiation to kill cancer cells you kill healthy cells so you get: hyperphosphotemia, hyperkalemia, hypocalcemia)
Hyperleukocytocis >100,000 WBC
Capillary obstruction
***Petechiae, Fever, Fatigue

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5
Q

Leukemia Acute Lymphocytic Leukemia (ALL):
Diagnostic evaluation

A
  • Suspected from the history, physical manifestations, and a peripheral blood smear that contains immature forms of leukocytes, frequently in combination with low blood counts.
  • Definitive diagnosis: *bone marrow aspiration or biopsy. Lumbar Puncture to determine CNS involvement
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6
Q

Leukemia Acute Lymphocytic Leukemia (ALL):
Treatment & Side Effects of Treatment

A
  • Chemotherapy: 1st option
    — Induction phase: 4-5 types of chemo agents for 1 month
    — Intensification phase: give a new type of stronger med in case there are tumor cells that are hiding/ got missed
    — Delayed intensification phase: give a lower dose of chemotherapy/ CNS prophylactic Therapy: give chemo intrathecally
    — Maintenance phase: should be in remission: bone marrow aspiration is (-) for leukoblasts. Given for 3 years
  • High dose Steroids: prednisone: immunosuppressant
  • Radiation therapy: if really concentrated in a specific area (like the spleen)
  • Infection/neutropenia: fever
  • ANC- segs+bandsx1000
  • Hemorrhage
  • Cystitis: s/s of chemotherapy (hemorrhagic cystitis)
  • Anemia
  • Nausea/Vomiting: ondansetron (Zofran)
  • Altered nutrition: High calorie/ High Protein
  • Mucosal Ulceration: entire GI tract
  • Neurologic problems
  • Alopecia: hair loss (help adolescent with body image issues; help find wig)
  • Steroid Effects
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7
Q

Wilms’ tumor

A
  • Is a fast growing solid tumor that is asymptomatic. It is a firm lobulated mass on or inside the kidney
  • Peak incidence between 2-3 years
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8
Q

Wilms’ tumor
Treatment/ nursing considerations

A
  • Treatment & prognosis based on stage
    — Stage is based on size and how much it has metastasized
    — Grading based on abnormalities of the cells; mutations/ genetic markers; do a biopsy
  • Requires surgical removal (outside of kidney) inside kidney= remove entire kidney), Chemotherapy, and possibly radiation
    — Radiation is last choice: because you can develop secondary type of cancer from radiation
  • **Do not palpate Abdomen.
    — Pushing on the tumor can break off pieces of tumor because it is fragile and could spread
  • Preserve kidney function
    — BUN/Cr, strict I&O, Foley cath, don’t give meds that are nephrotoxic (some antibiotics; measure peak and trough)
    — Kidneys release renin; increased renin = increased BP; monitor BP
    — Releases erythropoietin: stimulates RBC production; decrease kidney function= anemia
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9
Q

Retinoblastoma

A

Intraocular malignancy of the retina
40% of cases are hereditary- autosomal dominant gene.
Peak incidence 2 years old

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10
Q

Retinoblastoma S/S

A

**leukokoria- white pupil and absent red reflex

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11
Q

Retinoblastoma treatment

A
  • radiation, surgery, laser therapy and possibly chemotherapy, remove eye.
  • 90% survival rate.
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12
Q

Neuroblastoma

A
  • Any solid tumor occurring outside of the cranium.
  • Most commonly in the abdomen
  • Location of the mass determines the symptoms
  • Most common tumor in infants to 12 months old
  • Treatment- radiation, chemotherapy and surgery
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13
Q

Bone Tumors:

OSTEOSARCOMA

A
  • Malignant tumor of long bone near the growth plate involving rapidly growing bone tissue
  • Occurs mostly in male teens
  • Peak incidence during (puberty) rapid growth
  • Treatment- surgical - amputation, chemotherapy
  • Pain, swelling, decreased ROM, limp, pathologic fracture
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14
Q

Bone Tumors:
EWING SARCOMA

A
  • occurring in the bone marrow of diaphyseal seal
  • Occurs in older school age and young adolescents
  • Treatment- radiation & chemotherapy. Amputation last resort
  • Pain, swelling, decreased ROM, limp, pathologic fracture
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