Exam 3 - Leukemia and other Disorders Flashcards

1
Q

What is a neoplastic disorder involving WBC and no solid tumor?

A

Leukemia

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2
Q

Is idiopathic in children

A

Leukemia

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3
Q

Leukemia does what to the production of other normal cell leading to anemia

A

Suppresses production

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4
Q

In leukemia, the nonfunctional cells that multiply uncontrollably in the bone marrow do what?

A

Cause pain and suppress the production of other normal cells leading to anemia

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5
Q

Etiology: previous chemo, exposure to radiation, some viruses, chromosomal anomaly, and chemicals

A

Leukemia in ADULTS

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6
Q

Large quantities of WBC are released into the general circulation and then&raquo_space;>?

A

infiltrate lymph nodes, spleen, liver, brain, and other organs

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7
Q

Acute leukemia:

*high proportion of very immature nonfunctional cells (blast cells) in the bone marrow and peripheral circulation

*onset usually is abrupt

*marked signs and complications

A

Chronic leukemia:

*higher proportion of mature cells (although they may have reduced function)

*insidious onset and MILD sign

*better prognosis than with acute

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8
Q

Leukemia S/S

A

*multiple infections (often unresponsive to
treatment
*severe hemorrhage (brain or digestive
tract)
*anemia
*bone pain (severe and steady even at rest)
*weight loss, fatigue (hypermetabolism;
keep an eye on H&H)
*lymph nodes, spleen, liver are often
enlarged and may cause discomfort
*fever (hypermetabolism or infection)

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9
Q

Leukemia Diagnosis:

A

Peripheral blood smears - show immature leukocytes and altered numbers of WBCs

Anemia, thrombocytopenia

Bone marrow biopsy - confirms the diagnosis

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10
Q

Leukemia management:

A

Chemotherapy
Biologic therapy (chronic forms)
Blood product replacement
Adequate hydration and nutrition
Bone marrow transplant

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11
Q

More abrupt in children

A

Acute leukemia

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12
Q

gradual onset

A

chronic leukemia

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13
Q

Functions of the lymphatic system

A

*return excess interstitial fluid and protein to the blood
*filter and destroy unwanted material from the body fluids
*initiate an immune response
*interacts with all other body systems

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14
Q

similar in structure to veins, but thinner walls, more valves, contain nodes at certain intervals

More permeable allowing passage of larger substances and protein

A

Lymphatic vessels

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15
Q

Tonsils-protect against bacterial infection in the area of the opening between the nasal and oral cavities

A

Lymphoid Tissue

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16
Q

Containing many lymphocytes and macrophages
Dispersed when there is infection
Situated along all lymphatic and blood vessels
Help to recognize pathogens

A

Lymph Nodes

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17
Q

On the left side of the body
Defense, hematopoiesis, and RBC and platelet destruction, as well as serving as a reservoir for blood

A

SPLEEN

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18
Q

Ruptured spleen

A

massive bleed

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19
Q

overloaded spleen

A

high infection

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20
Q

Thymus gland

A

Most active at until birth
Final site of lymphocyte development before birth
Secretes hormones after birth that enable lymphocytes to develop into mature T cells (attack foreign cells)

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21
Q

clear, watery, isotonic fluid that is circulated in the lymphatic vessels

22
Q

fluid that is not absorbed by the cells or the capillaries tend to accumulate in the interstitial space (swelling

A

Interstitial fluid

23
Q

As interstitial fluid builds it will drain into the lymphatic vessels and become _________?

24
Q

enlarged lymph nodes due to inflammation or infection

A

Lymphadenopathy

25
Diagnosis for Lymphadenopathy
Exam Ultrasound Fine-needle biopsy PET-CT (light up other lymph nodes to see what's up)
26
Treatment for Lymphadenopathy
treat the cause
27
*inflammation or infection of lymph nodes *common signs of another disease (bacterial, viral, malignancies) *manifests as swollen lymph nodes >an increase in size and extent over time usually indicates cancer *generalized lymphadenopathy >systemic symptoms instead of localized painful swelling
Lymphadenopathy
28
Malignant neoplasms involving lymphocyte proliferation in the lymph nodes. Specific causes of ___________ have not been identified, but there is a higher incidence in adults who received radiation treatments during childhood
Lymphomas
29
Usually affects adults age 20-40 Most often starts in the lymph nodes in the upper part of the body
Hodgkin Lymphoma
30
Patho-initially a single group of lymph node lower extranodal involvement that non-Hodgkin Orderly contiguous spread (works its way down)
Hodgkin Lymphoma
31
T-lymphocytes defective and the lymphocyte count is decreased-increased R/F recurrent infections T lymphocytes active in immune response increased risk of infection
Hodgkin Leukemia
32
DX marker-Reed Sternberg cells (no cells if no _____________) 1st sign enlarged lymph nodes, often cervical, that is painless and nontender
Hodgkin Lymphoma
33
S/S: Splenomegaly other enlarged lymph nodes general cancer signs (fatigue, anorexia, weight loss) Pruritis (itchy) frequent infections
Hodgkin Lymphoma
33
Ann Arbor Staging System (how we identify what is going on) Treatment: radiation chemotherapy surgery
Hodgkin Lymphoma
34
Usually seen in adults over 60 seeing more frequently in patients with HIV Tends to be more widespread that Hodgkin Lymphoma more lymph nodes involved extranodal involvement common No Reed-Sternberg Cells! Most cases involve B lymphocytes Risk factor: history of chemo; cancer unorganized widespread metastasis
Non-Hodgkin Lymphoma
35
S/S: 1st symptom-enlarged painless lymph node Can be more difficult to treat due to widespread metastases and extranodal involvement Follow Ann Arbor Staging
Non-Hodgkin Lymphoma
36
Multiple Myeloma
Malignancy involving the PLASMA cells (mature B lymphocytes involved in production of antibodies) Increased number of malignant plasma cells replace the bone marrow and erode the bone Blood cell and antibody production is impaired
37
Multiple tumors in bone destruction develop in the vertebrae, ribs, pelvis, and skull Pathologic or spontaneous fractured Hypercalemia occur as bone is destroyed Tumor cells can spread throughout the body-lymph nodes and organs
Multiple Myeloma
38
Insidious onset, usually well advanced by the time it is discovered Manifestations: frequent infections (antibody involvement) pain related to bone involvement, present at rest and with activity pathologic fractures anemia and bleeding tendencies (blood cell production impaired) proteinuria and kidney failure
Multiple Myeloma
39
Management: Chemotherapy Supportive care analgesic for bone pain renal support blood transfusions
Multiple Myeloma
40
Tissues in the extremities SWELL due to obstruction of the lymphatic vessels and accumulation of lymph
Lymphedema
41
Etiology: Primary - congenital Secondary to cancer, tumor, radiation therapy, damage during surgery, removal of lymph nodes
Lymphedema
42
Manifestations: *swelling, initially soft, but progresses to firm, painful and unresponsive to treatment *increased risk of frequent infections
Lymphedema
43
Management: Bed rest, massage, ELEVATION Diuretics Surgical options when severe
Lymphedema
44
Form of lymphedema resulting from infestation and blockage of lymph vessels by a parasitic worm (filaria) Extreme swelling can be so significant that the extremity looks like an elephant's leg
Elephantiasis
45
S/S: thickening of subcutaneous tissue, frequent infections, skin ulcerations, fever Management: skin care and elevation antiparasitic drugs surgery to place shunt for fluid
Elephantiasis
46
Lymphoproliferative disorder (not cancer)-overgrowth of lymphoid tissue Associated with higher risk of Lymphoma
Castleman Disease
47
______________-affects one lymph node s/s: depend on location-large lump, difficulty breathing or eating, weight loss/poor appetite, cough Tx-remove the node if possible; if not, steroids or radiation to shrink/destroy node
Unicentric - Castleman Disease
48
____________-affects multiple lymph nodes>>decreased immune response Tx- more difficult, too many nodes to remove; meds-steroids, anticancer, immunomodulating
Multicentric - Castleman Disease
49
LEUKEMIA DIAGNOSIS AND MANAGEMENT
50
LEUKEMIA SIGNS & SYMPTOMS