WBC disorders Flashcards

1
Q

infectious mononucleosis “mono”

A

self-limiting lymphoproliferative disorder–lymphocytes growing too much; infection of B lymphocytes caused by Epstein-Barr virus

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2
Q

Mono transmission

A

EBV-contaminated saliva most prevalent in teens/young adults bc spread through saliva and fluid

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3
Q

mono onset

A

insidious, 4-8 week incubation period

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4
Q

mono sx

A

nonspecific–lymphoadenopathy (swollen nodes in neck and armpit), hepatitis (swollen liver), splenomegaly (swollen spleen), tired, throat sore, body ache

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5
Q

mono labs

A

inc WBCs; 95% lymphocytes–very high

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6
Q

mono progression

A

2-3 weeks of acute phase; 2-3 months lethargy, debility

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7
Q

mono tx

A

treat sx, supportive, sleep, hygiene, hydration

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8
Q

myelodysplastic sx

A

group of related hematologic dx char by chx in quantity or quality of bone marrow elements; blood cells could not mature, accum, or short life

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9
Q

myelodysplastic sx

A

cytopenias (low blood count)–anemia, infection and spon bleeding or bruising

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10
Q

who does myelodysplastic sx affect?

A

most over 65

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11
Q

myelodysplastic sx cause

A

unknown, maybe enviro trigger

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12
Q

myelodysplastic sx diagnosis

A

labs and bone marrow biopsy

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13
Q

myelodysplastic sx tx

A

depends on severity, supportive, chemo, GCSF, erythrypoietin, bone marrow transplant

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14
Q

leukemias

A

Malignant neoplasms of cells originally derived from a single
hematopoietic cell line

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15
Q

Leukemic cells char and locations

A

Are immature and unregulated (undifferentiated), Proliferate in bone marrow, Circulate in blood, Infiltrate spleen, lymph nodes

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16
Q

how are leukemias classified?

A

according to their predominant cell type and acute vs chronic condition

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17
Q

acute lymphotic (lymphoblastic) leukemia

A

most common childhood leuk; higher survival rate

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18
Q

chronic lymphocytic leukemia

A

most common in older adults; Relatively mature lymphocytes that are immunologically incompetent; S&S: fatigue, wt loss, anorexia, infections

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19
Q

acute myelocytic leukemia

A

mostly an adult disease; low 5-year survival rate

20
Q

lymphocytic leukemia

A

affects lymphoid stem cells especially lymphocytes

21
Q

myelocytic

A

affects myeloid stem cells esp granulocytes

22
Q

chronic myelocytic leukemia

A

Leukocytosis with immature cell types (presents with increased granulocyte count); S&S: fatigue, wt loss, diaphoresis, bleeding, abdominal discomfort from splenomegaly

23
Q

cause of leukemia

A

unknown; inc exposure to radiation

24
Q

Leukemic cells

A

Are an immature type of WBC; Capable of increased rate of proliferation/have prolonged life
span; Cannot perform function of mature leukocytes → are ineffective
as phagocytes; Interfere with maturation of normal bone marrow cells (including
RBC & platelets)

25
acute leukemias
sudden, stormy onset; dec mature WBC, dec RBC, dec platelets, kids refuse to walk and bone pain
26
acute leukemia diagnosis
based on blood/bone marrow tissue; find immature WBCs (blasts), may constitue 60-100% of cells
27
Chronic leukemia
more insidious onset, often diagnosed during routine blood check
28
leukemia tx
goal is remission; start with cytotoxic chemo, move to stem cell transplant (bone)
29
Risks of leukemia tx
infection, rejection, relapse
30
Malignant lymphomas
Neoplasms of cells derived from lymphoid tissue * Hodgkin Disease * Non-Hodgkin Disease
31
Hodgkin disease
Characterized by painless, progressive, rubbery enlargement of a single node or group of nodes – usually in neck area and nonspecific sx; Reed-Stenberg cell
32
Reed-Stenberg cell
distinctive tumor cell found with lymph biopsy; distinctive--for Hodgkins diagnosis
33
Hodgkins cause
unknown, maybe EBV, genetic predis, exposure to toxins
34
Hodgkin diagnosis
Diagnosis: peripheral blood analysis, lymph node biopsy, bone marrow exam, radiographic evaluation (CT, MRI, PET)
35
Hodgkins tx
Chemotherapy- standard- doxorubicin (Adriamycin), bleomycin, vinblastine, and dacarbazine; 2-8 cycles * Radiation * Stem Cell Transplant
36
Non-Hodgkin disease
Neoplastic dx of lymphoid tissue; spreads early to liver, spleen, bone marrow; char by painless, superficial lymphadenopathy, also extranodal sx; caught later, harder to diagnosis bc no distinguishing cell type
37
Etiology of non-Hodgkin
unknown
38
Non-Hodgkins diagnosis
similar to Hodgkins, inc extranodal sites--lymph tissue at non-lymph sites
39
Non-Hodgkins tx
chemotherapy, radiation, refractory cases- stem cell transplant; Rituximab (Rituxan), ibritumomab tiuxetan (Zevalin), tositumomab (Bexxar) & others
40
Multiple myeloma (Plasma cell myeloma)
atypical proliferation of "M" protein immunoglobulin which is a monoclonal antibody; inc osteoclast activity (bone b/d), can't maintain humoral immunity--get sicker
41
Myeloma sx
bone pain/frac, also sx r/t impaired RBC and WBC count
42
Who is more likely to get myeloma
men, around age 65, African Americans
43
Myeloma CM
slow and insidious; anemia, bleeding, hypercalcemia from seeping out of bones, skeletal pain (often 1st sx)
44
Multiple myeloma diagnosis
lab, radiography, bone marrow exam; look for bone b/d and monoclonal antibody protein serum and urine; pancytopenia (all cells dec), hypercalcemia, elevated serum creatinine, Bence Jones proteins in urine; Xray osteolytic lesions
45
Multiple myeloma tx
watch, corticosteroids, promote bone health, chemo, stem cell transplants, adequate hydrations, biophosphates