4.3 Hemato-oncologic Disorder Flashcards

1
Q

Leukemia

A
  • Unregulated proliferation of immature/abnormal WBC’s in bone marrow
  • Malignant neoplasm of hematopoietic cells
  • Proliferation occurs in bone marrow then spreads to lymph nodes, spleen, liver, etc
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2
Q

Leukemia Types

A
  • Characterized by predominant cell types

Lymphocytic vs Myelocytic
- Lymphocytic usually affects B-Cells and bone marrow stem cells
- Myelocytic affects blood forming cells in the bone marrow

Acute vs Chronic

Acute - Rapid increase of immature blood cells (usually blast cells)
(Acute Lymphocytic Leukemia or Acute Myelocytic Leukemia)

Chronic - Excessive buildup of mature but abnormal white blood cells
(Chronic Lymphocytic Leukemia or Chronic Myelocytic Leukemia)

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3
Q

Leukemia Types

A

Acute Lymphoblastic Leukemia (ALL) - Most common in young children

Chronic Lymphoblastic Leukemia (CLL) - Most common in adults 55+
- Incurable. Affects men more than women

Acute Myelogenous Leukemia (AML) - Most common in adult men
- Treated with chemotherapy

Chronic Myelogenous Leukemia (CML) - Mainly affects adults
- Treatment is Gleevec

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4
Q

Manifestations of Leukemia

A
  • Frequent Infections
  • Enlarged Lymph Nodes (Lymphadenopathy)
  • Enlarged Liver/Spleen
  • Weakness/Fatigue
  • Low-grade fever and night sweats
  • Generalized pain (bone pain)
  • Tachycardia, Hypotension
  • Bleeding
  • CNS involvement
  • Emboli
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5
Q

Diagnosis of Leukemia

A
  • Bone marrow biopsy (large number of immature leukocytes)
  • Low HgB, Hct, RBCs, Platelets
  • High ESR, Immature WBCs
  • Prolonged PT, PTT, INR
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6
Q

Treatment

A

ALL
- Chemotherapy (Vinca Alkaloids)
- Corticosteroids (Dexamethasone)
- Hematopoietic Stem Cell Transplant (HSCT)
- Monoclonal Antibodies

CLL
- “Watch and wait”
- Immunotherapy
- Chemotherapy
- Monoclonal Antibodies

AML
- Aggressive chemotherapy (induction therapy)
- HSCT
- Palliative Care

CML
- Tyrosine Kinase Inhibitor (Gleevec)
- HSCT
- Aggressive Chemotherapy for “BLAST CRISIS”

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7
Q

Tumor Lysis Syndrome (Complication of Chemotherapy)

A
  • Massive destruction of cells which releases intracellular electrolytes and fluids into systemic circulation
  • Increased uric acid, potassium, and phosphate in the blood
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8
Q

Goals and Education and of Leukemia

A

GOALS

  • Absence of pain
  • Maintenance of nutrition
  • Activity tolerance
  • Understanding the disease

Interventions are aimed at detecting changes in patients condition, see if they need transfusion, and monitor for infection.

EDUCATION
- Recognize symptoms of occult bleeding or infection
- Prevent constipation
- Use electric razor
- Increase fluid intake

IMPORTANT NOTE
- May not have classic signs of infection. Sore throats or diarrhea need to be followed up on

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9
Q

Lymphoma

A
  • Cancer of lymphocyte DNA which leads to malignant transformation
  • Uncontrolled excessive malignant cells get produced in the lymph nodes or lymph tissue of the stomach/intestines that create tumors.
  • Usually starts in lymph nodes but can travel to spleen, GI tract, or bone marrow
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10
Q

Hodgkin’s Lymphoma

A
  • Proliferation of Reed Sternberg Cells in lymph nodes
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11
Q

Non-Hodgkin’s Lymphoma

A
  • Any lymphoma that does not contain Reed-Sternberg Cells
  • It frequently originates outside the nodes then spreads to nodes

Etiology - Unknown (possibly due to impaired immune system or virus)
Pathophysiology - Progressive clonal expansion of B, T, and Natural Killer Cells

Diagnosis
Lymph Node Biopsy
Bone Marrow Biopsy for Staging
Blood Studies
Chest/Abdomen CT Scans

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12
Q

Manifestations of Lymphoma

A
  • Lymphadenopathy
  • Anorexia/Weight Loss
  • Bone Pain
  • Dysphagia
  • Dyspnea/Cough
  • Recurrent Fever
  • Severe Pruritis
  • Hepatomegaly/Splenomegaly

MAJOR ONES
- Enlarged, Non-Tender, Firm, Movable Lymph Nodes
- Fatigue, Dyspnea, Recurrent Fever

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13
Q

Diagnosis

A

X-Ray
- Check for enlarged lymph nodes

Positron Emission Tomography (PET) Scan
- Check for malignant cells

Bone Marrow Aspiration
- Check for cell types (staging)

Lymph Node Biopsy
- Check for malignant cells or Reed-Sternberg cells

Increased Alkaline Phosphate
- Indicates it has spread to bone/liver

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14
Q

Treatment for Hodkin’s Lymphoma

A

Radiation Therapy for early onset

Chemotherapy for advanced lymphoma that do not respond to radiation

HSCT

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15
Q

Treatment for Non-Hodgkin’s Lymphoma

A
  • Wait until symptoms develop
  • RARELY HSC
  • Radiation is therapy of choice for non-aggressive localized lymphoma
  • Cranial radiation or intrathecal chemotherapy if CNS is involved
  • Immunotherapy

INTERVENTIONS
- Monitor VS, I&O, Daily Weight, Bleeding
- Skin and mouth care to prevent breakdown of oral mucosa

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16
Q

Multiple Mylenoma

A
  • Malignant disease of B Lymphocytes (plasma cells)
  • Production of M Protein and Bence Jones Protein
  • FIRST SIGN IS BONE PAIN (these cancer cells proliferate in bone marrow and cause bone lesions)
  • Associated with agent orange exposure in Vietnam

MANIFESTATIONS
- BONE PAIN in back and ribs
- Pathologic fractures from bone destruction
- Prone to infection (decreased humoral response)
- Hypercalcemia from increased bone resorption
- Osteolytic Lesions - Plasma cell tumors in the bone that cause breakdown

DIAGNOSIS
- Blood tests, marrow exam
- Lytic Bone Lesions
- Presence of M-Protein and Bence Jones Protein in Urine

17
Q

Treatment for Multiple Myeloma

A
  • Initial treatment tries to reduce tumor burden (reduce myeloma cells and reduce monoclonal protein) without damaging stem cells (autologous HSCT)
  • Corticosteroids induce apoptosis in melanoma cells and decrease bone pain (dexamethasone)