TLO 103c Neoplastic Flashcards

1
Q

Neoplastic

neoplasm?

A

Neoplasm:
any abnormal growth of new tissue, benign or malignant
Also called tumor

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2
Q

How does cancer spread, two ways?

A

Invasion:
cancer cells grow in an unrestricted disorderly way at site of origin
Metastasis:
cancer cells grow in other sites than that of which it originated

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3
Q

Malignant of cancer

A

Malignant of cancer
A group of >200 diseases characterized by uncontrolled and unregulated growth of cells

Characteristic of malignant neoplasm
Poorly differentiated
Capable of metastasis
Possible reoccurrence
Moderate to marked vascularity
Infiltrative and expansive mode of growth
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4
Q

Benign characteristic, noncancerous

A
Usually encapsulated
Normally differentiated
No metastasis
Rare reoccurrence
Slight vascularity
Expansive growth
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5
Q

Development of cancer

A

Development of cancer
Initiation:
mutation in cells genetic structure so that it can develop a clone
Promotion:
Reversible proliferation of the altered cells
Progression:
Increased growth rate of the tumor, increased invasiveness, increased metastasis

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6
Q

Carcinogens defined

A

Carcinogen:

Cancer causing agents capable of producing cellular alterations

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7
Q

Immune system

A

Immune system:
Role: recognition and destruction of tumor cells

Can distinguish normal from abnormal cells

  • transplant organs can be recognized as foreign, rejection can occur
  • because cancer cells develop from normal human cells that mutate, the response against cancer cells may not be sufficient to kill cells

Immune response to malignant cells:
Cytotoxic T cells: role in resisting tumor growth by killing tumor cells. Produce cytokines which stimulate T cells, natural killer cells, B cells and macrophages

Natural killer cells: directly lyse tumor cells

Macrophages: nonspecific lytic of tumor cells

B lymphocytes: produce antibodies that bind to tumor cells and kill them; detects in serum/saliva

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8
Q

Oncofetal Antigens, tumor markings

A

Oncofetal antigens: useful marker for cancers
Found on both the surfaces/inside of cancer cells and fetal cells
Cells shift to immature metabolic path associated with fetal period of life. Cell regains embryonic capability to differential into many different cell types

Carcinoembryonic (CEA): useful marker for cancers
Found on surface of cancer cells from the GI tract, fetal gut, liver, pancreas, normally disappears in last 3 months of fetal life.
Monitor therapy

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9
Q

Developmental of cancer in children

A

Alterations in normal DNA predispose the child to cancer or chromosomal abnormalities cause an inherited disposition
Failure of the immune system to distinguish between normal and abnormal cells
Inactivation of tumor suppressor genes

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10
Q

Oncofetal antigens tumor markers

A

Oncofetal antigens tumor markers
A-fetoprotein (AFP) is produced by malignant liver cells and fetal liver cells
AFP detection is of value in tumor detection and tumor progression
Elevated in testicular carcinoma, viral hepatitis and nonmalignant liver disorders
Diagnostic is primary cancer of the liver, hepatocellular
Produced with metastatic liver growth

Other oncofetal antigens:
CA 125: ovarian carcinoma
CA 19-9 pancreatic and gallbladder cancer
CA 15-3 and CA 27-29 breast cancer

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11
Q

Cancer classifications of tumors provide a standardized method

A

Classification of tumors provide a standardized method to:
Communicate the status of the cancer to health care team
Assist in determining the most effective treatment plan
Evaluate the treatment plan
Predict prognosis
Compare like groups for statistical purposes

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12
Q

Carcinogens

Chemical

A

Carcinogens
Chemical
Chemical: drugs that interact with DNA

Chemical:
Drugs: alkylating agents (Cytoxan): secondary leukemias are refractory to induction of remission with combination chemotherapy

Immunosuppressive agents: secondary leukemias has been observed in patients with transplant surgery or immunosuppressive drugs.

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13
Q

Carcinogens

Radiation

A

Carcinogens
Radiation
The dose of radiation that causes cancer is unknown
Debate surrounding the effects of low dose exposure over time
Leukemia, lymphoma, thyroid cancer and others increased in Hiroshima and Nagasaki after atomic bomb
More bone cancer in occupations as radiologists, radiation chemists and uranium miners.
More thyroid cancer in person who received radiation to the head/neck area
Ultraviolet radiation, more melanoma, squamous and basal cells cancers

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14
Q

Carcinogens

Viral

A

Carcinogens
Viral
person with AIDS have a high incidence of Kaposi sarcoma
Hepatitis B has been linked to hepatocellular carcinoma
Human papilloma virus induces lesions that are capable of progressing to cervical cancer

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15
Q

Cancer tumors are classified by anatomic site

A

Cancer tumors are classified by anatomic site

Identified by the tissue of origin:
Behavior of the tumor (benign or malignant):

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16
Q

Extent of disease (staging)

A

Clinical staging
Determined the anatomic extent of the malignant disease
Determines the treatment options
Stage 0: cancer is situ
Stage I: localized tumor growth with cells of tissue of origin
Stage II: limited local spread
Stage III: extensive local and regional spread
Stage IV: metastasis

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17
Q

Cancer early warning signs

CAUTION

A
Change in bowel or bladder
A lesion that does not heal
Unusual bleeding or discharge
Thickening or lump in breast or elsewhere
Indigestion or difficulty swallowing
Obvious changes in wart or mole
Nagging cough or persistent hoarseness
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18
Q

Cancer classification TNM

A

TNM classification system: determines the anatomic extent of disease and tumor involvement according to 3 parameters
T: Tumor, how many 1-4
N: lymph nodes, how many are positive 1-4
M: metastasis, how many areas spread to 1-4

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19
Q
Cardinal s/s of cancer in children
Overt signs (obvious signs)
A
Overt signs:
A mass
Purpura (A rash of purple spots due to small blood vessels leaking blood into the skin, joints, intestines, or organs)
Pallor
Weight loss
Whitish reflex in eye
Vomiting in early morning
Recurrent or persistent fever
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20
Q

Cardinal s/s of cancer in children

Covert (not openly acknowledged or displayed)

A

Covert: (not openly acknowledged or displayed)
Bone pain
HA
Persistent lymphadenopathy (inflammatory)
Change in balance, gait or personality
Fatigue, malaise

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21
Q

Diagnostic studies

A
Bone, liver, lung brain scan
US
CT
MRI
PET
Mammography
Chest x-ray
Endoscopic exam, UGI, colonoscopy
Cytology, Pap test
Tissue biopsy
CBC
Liver function
Tumor markers
Genetic markers
Bone marrow exam
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22
Q

Therapies for pediatric cancer

A
Chemo
Radiation
Surgery
Hematopoietic stem cell transplant: allogenic (matched donor), autologous (child's own)
Biologic response modifiers
Steroid
Complementary, alternative medicine
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23
Q

Chemo nursing inplications

A

The use of chemicals as a systemic treatment for cancer. Chemo therapy drugs non selectively kill rapidly dividing cells. Tumors can develop immunity to chemo agents

Chemo agents in addition to killing cancer cells
Affect bone marrow production
GI tract and the integumentary system

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24
Q

Radiation therapy nursing implications

A

Radiation therapy nursing implications
Causes damage to the cells and stops them replicating
In a developing child normal cells develop may not be complete
Radiation to the brain causes alteration in cognitive level
Bone growth is altered if radiation is delivered to the areas of growth potential

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25
Chemo side effects
``` Chemo side effects: Bone marrow suppression Alopecia Malaise/fatigue Nausea Vomiting Anorexia Stomatitis (oral, rectal sores) ```
26
Radiation side effects
``` Radiation side effects: Skin reactions (burns, redness) Fatigue Bone marrow suppression Nausea Vomiting Anorexia Mucositis (oral sores) ```
27
Leukemia
Broad term for group of malignant disease of bone marrow and lymphatic system Most common childhood cancer Peak onset 2-6 years old > in males and Caucasians Lymphoid leukemia 80% survival rates Acute nonlymphoid leukemia has 50% survival rate
28
Leukemia defined
Leukemia is an abnormal proliferation of immature white blood cells which compete with normal cells for space and nutrients Bone marrow production is suppressed which results in low numbers of WBC, RBC and platelets
29
Leukemia clinical manifestations
``` Liver and spleen are most effected (vascular organs) Acute form: leukocyte count is low S/S: Anemia Neutropenia Thrombocytopenia ```
30
Leukemia diagnostic
H&P Peripheral blood smear: contains immature forms of leukocytes, low blood count Bone marrow aspirate/biopsy: flow cyometry of cells in bone marrow Lumbar puncture to determine CNS involvement
31
Brain tumor signs
Infant may be irritable, lethargic, feed poorly, have increased head, bulging fontanels Young child loss of developmental milestones School age have declining academic performance, fatigue, personality changes, seizures Older children: HA upon waking, vomiting
32
Consequences of bone marrow disfunction
Decrease RBC= anemia; neutropenia= infection | Decrease platelets= bleeding tendencies
33
What are the clinical manifestations related to bone marrow dysfunction?
Pallor, fatigue, fever, hemorrhage, fractures, pain
34
How are the liver, spleen and lymph glands effected?
Infiltration, enlargement, eventual fibrosis (scarring) | Manifestations: hepatomegaly, splenomegaly, lymphadenopathy
35
How does leukemia impact CNS?
Increased ICP, meningeal irritation
36
What are the manifestation of hypermetabolism caused by leukemia?
Cell deprivation of nutrients by invading cells lead to muscle wasting, weight loss, anorexia, fatigue
37
Brain tumor diagnostic
``` MRI CT EEG Lumbar puncture Biopsy ```
38
Osteosarcoma what is it
The most common primary bone lesion in children Originates from the bone producing cells that invade the medullary canal of the bone, incidence is higher in the most rapidly growing bones in adolescence Goals of therapy: remove tumor, prevent spread
39
Leukemia four phases?
Induction therapy: achieves complete remission or less than 5% leukemia cells in bone marrow CNS prophylactic therapy: prevents leukemia cells form invading CNS Consolidation/intensification therapy: eradiation prevents emergence of resistant leukemic clones Maintenance therapy: maintain remission phase
40
Osteosarcoma sites
Primary tumor sites are in the metaphysis adjacent to the epiphyseal plate of long bones Other sites: tibia, humerus, pelvis, jaw, phalanges Higher in lower extremities
41
Leukemia treatment
Hematopoietic stem cells transplant: success with ALL and AML. Capable of differentiating into specialized calls. ``` Donors: antigen matched related donors matched unrelated mismatched donors obtained from related or unrelated donors or umbilical cord blood ``` ``` Transplant cons: Significant morbidity and mortality Graft vs host disease Overwhelming infection Severe organ damage ``` ``` Prognosis: long term survival depend on the following initial WBC count Child's age at diagnosis Type of cell involved Gender of child Karyotype analysis ```
42
Osteosarcoma clinical findings
Pain, mass, limping, limited ROM, pathological fractures
43
Osteosarcoma treatment
Surgery: biopsy, limb salvage or amputation Chemo Radiation, used only in the palliative pain control in the advanced patient
44
Osteosarcoma nursing care
``` Depend on type of surgery Post-op; emotional support Prepare for alopecia Permanent prosthesis fitting 6-8 wk posts op Elavil for phantom leg pain Physical therapy Planning for return to school ```
45
Ewing's sarcoma
Arises in the marrow spaces of the bone Tumor originates in the shaft of long and trunk bones Most common site: femur, tibia, fibula, humerus, ulna, vertebrae, scapula, ribs, pelvic and skull 2nd most common bone tumor seen in children
46
Ewing's sarcoma treatment
Radiation, chemo Amputation if radiation causes deformity, loss of function Vincristine, actinomycin D, cyclophosphamide, ifosfamide, etoposide, doxorubicin Prognosis: new chemotherapy agents have increased 3 years survival to 80%
47
Ewing's sarcoma nursing care
Psychological adjustment Prepare pt and family for bone marrow aspiration, surgical biopsy, radiation Skin care Encourage loose fitting clothing Protect site from sunlight/temperature changes Physical therapy Prepare for alopecia, N/V, peripheral neuropathy, possible cardiotoxic side effects
48
Wilm's tumor what is it? diagnostic
``` Wilm's tumor or nephroblastoma (kidney cancer) One or both kidneys involved Diagnostic: H&P Ab swelling/mass Ab US Ab/chest CT Hematologic studies Urinalysis Determine kidney function on opposite side ```
49
Wilm's tumor pre-op and post-op
``` Pre-op: Surgery in 24-48 hr of admit BP, hypertension due to excess in renin production Do not palpate ab, post sign above bed Radiation/chemo teaching ``` ``` Post-op: Recover is rapid GI activity BP, urine output, signs of infection Pulmonary hygiene Protect kidney that is left ```
50
Hodgkin's
A neoplastic disease that originates in the lymphoid system | Most common: asymptomatic enlarged cervical or supraclavicular lymphadenopathy
51
Hodgkin's classified
``` A= asymptomatic B= 3 symptoms: Fever 100.4 or higher for 3 days Drenching night sweats Unexplained loss of body weight over 6 mo ``` ``` Cough Ab discomfort Anorexia N/V Pruritus Fatigue Non painful lymph node enlargement ```
52
Hodgkin's treatment
``` Radiation Chemo Splenectomy in some cases: Prophylactic antibiotics Immunizations against pneumococci and meningococci ```
53
Retinoblastoma
Can be unilateral or bilateral Caused by mutation in gene Hereditary retinoblastomas are transmitted as an autosomal dominate trait
54
Retinoblastoma diagnostic
Ophthalmologist exam under general anesthesia | US, CT
55
What is the most common signs of retinoblastoma?
White eye reflex
56
What is the 2nd most common sign of retinoblastoma
Strabismus | condition in which the eyes do not properly align with each other when looking at an object
57
What is another sign, often with glaucoma?
Red, painful eye
58
What is the late sign of retinoblastoma?
Blindness
59
Retinoblastoma nursing management
Pre and post op teaching Post op care of eye/socket care Preparing parents for post op facial appearance Post op enucleation (removal of the eye that leaves the eye muscles and remaining orbital contents intact): Facial features return to normal w/in 3 wk of prosthesis
60
Retinoblastoma prognosis
``` Survival rate 90% Long term concerns: decreased visual acuity facial disfiguration secondary tumor ```
61
Two forms of leukemia in children?
Two forms of leukemia in children? Classified by the type of WBC affected ``` Acute lymphoid leukemia (ALL) **most common: Stem cell or blast cell Lymphatic Lymphocytic Lymphoblastic Lymphoblastoid ``` ``` Acute nonlymphoid leukemia (ANLL): Granulocytic Myelocytic Monocytic Myelogenous Monoblastic Monomyeloblastic ```