E3 WBC disorders Flashcards

(41 cards)

1
Q

Infectious Mononucleosis “Mono”

A

-Self-limiting lymphoproliferative disorders
-Infection of B lymphocytes
-Atypical lymphocytes proliferate

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2
Q

Infectious Mononucleosis is caused by

A

Epstein-Barr virus (EBV)

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3
Q

Main mode of transmission for Infectious Mononucleosis

A

EBV contaminated saliva
“Kissing disease”
Also body fluids-Semen or blood/ Sex or organ transplant

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4
Q

What age group does Infectious Mononucleosis mainly effect?

A

adolescence/ young adults

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5
Q

Acute phase and Onset of Infectious Mononucleosis

A

Insidious, incubation 4-8 weeks
Acute phase 2-3 weeks
Some degree of debility/lethargy 2-3 months

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6
Q

Clinical manifestations of Infectious Mononucleosis

A

-Lymphadenopathy (swollen lymph nodes)
-Hepatits (swollen liver)
-Splenomegaly (swollen spleen)
-Extreme fatigue
-Fever
-Sore throat
-Body aches
-WBC increased and Lymphocytes increased

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7
Q

Treatment of Infectious Mononucleosis

A

Symptomatic & supportive
-Take tylenol & rest
-No vaccine
-Prevent by not kissing, sharing drinks, personal items

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8
Q

What is Myelodysplastic syndrome?

A

A group of related hematologic disorders characterized by a change in the quantity and quality of bone marrow elements

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9
Q

Who does Myelodysplastic syndrome usually effect?

A

elderly (65+)

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10
Q

Clinical manifestations of Myelodysplastic syndrome

A

-Cytopenias (low blood cell count)
-Anemia
-Infection
-Spontaneous bleeding or bruising

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11
Q

Etiology of Myelodysplastic syndrome

A

Unknown, maybe an environmental trigger

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12
Q

Diagnosis and treatment of Myelodysplastic syndrome

A

Diagnosis: Laboratory (CBC) & bone marrow biopsy
Treatment: Depends on severity-
-Supportive (Low grade/chronic)
-Granulocyte colony-stimulating factor (G-CSF)
-Erythropoietin (RBC prob)
-Chemo & Bone marrow transplant (severe)

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13
Q

What is Leukemias?

A

Malignant neoplasms of cells originally derived from a single hematopoietic cell line
aka immature WBCs that are unregulated or undifferentiated

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14
Q

Leukemic cells: (4)

A
  1. Are immature & unregulated
  2. Proliferate in bone marrow
  3. Circulate in blood
  4. Infiltrate spleen & lymph nodes
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15
Q

Who is most affected by Leukemia?

A

Children & adults

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16
Q

How is Leukemia classified?

A

According to their predominant cell type & whether the condition is acute or chronic
1. Acute Lymphocytic Leukemia (ALL): Most common childhood Leukemia
2. Chronic Lymphocytic Leukemia (CLL): Most common Leukemia in Older adults
3. Acute Myelocytic Leukemia (AML)
4. Chronic Myelocytic Leukemia (CML)

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17
Q

Myelocytic pathway

A
  1. Hematopoiesis
    Pluripotential stem cell
  2. Myeloid stem cells
  3. Granulocyte: macrophage stem cells
    4a. Granulocyte stem cells
    4b. Monocytic stem cells
    5a. Neutrophils, Eosinophils, & Basophils
    5b. Monocytes & Macrophages

*Immature granulocytes

18
Q

Lymphocytic pathway

A
  1. Hematopoiesis
    Pluripotential stem cell
  2. Lymphoid stem cells
  3. Lymphocytes (T-cells, B-cells, plasma cells)

*immature lymphocytes

19
Q

Cause of Leukemia

A

Unknown
Increased exposure to radiation

20
Q

Pathogenesis of Leukemic cells (4)

A
  1. Immature type of WBC
  2. Capable of increased rate of proliferation// have prolonged life span
  3. Can’t perform function of mature leukocytes (ineffective phagocytes)
  4. Interfere with maturation of normal bone marrow cells (including RBC & platelets)
21
Q

Acute Leukemia

A

-Sudden, stormy onset
-ALL: Mainly kids with high survival rate
-AML: adults with low survival rate
-S/S related to decreased (mature) WBC, RBC, & plateltes
-Bone pain, bruising, fever, fatigue, infection, kid may refuse to walk

22
Q

Chronic Leukemia

A

-More insidious onset
-No sudden pain onset
-May be discovered during routine check up of blood count
-CLL: Mainly older adults with high survival rate
-CML: adults & kids with slightly lower survival rate

23
Q

Chronic Lymphocytic Leukemia (CLL)

A

-Relatively mature lymphocytes that are immunologically incompetent
-S/S: fatigue, wt loss, anorexia, infections

24
Q

Chronic Myelocytic Leukemia (CML)

A

-Leukocytosis with immature cell types (presents with increased granulocytes count & splenomegaly)
-S/S: fatigue, wt loss, diaphoresis, bleeding, abdominal discomfort
-Age 40-50

25
Treatment of Leukemia
-Goal: attain remission -Cytotoxic chemotherapy -Stem cell transplant -Risks: Infection, rejection, relapse
26
What is Malignant Lymphoma? and the 2 types
-Neoplasms of cells derived from lymphoid tissue -Hodgkins & Nonhodgkins
27
Hodgkins disease is characterized by
painless, progressive, rubbery enlargement of a single node or group of nodes- usually in neck area
28
What is the distinctive tumor cell found with Hodgkins disease
Reed-Stenberg cell (Originate from B-cells in lymph nodes- they grow & spread in predictable manner)
29
Clinical manifestations of Hodgkins disease
Insidious onset, painless enlarged lymph nodes & other nonspecific symptoms -fever, night sweats, wt loss, malaise
30
Treatment of Hodgkins disease
Good treatment due to predication of growth -Chemotherapy -Radiation -Stem cell transplant
31
Non-Hodgkins disease is characterized by
Painless, superficial lymphadenopathy, extranodal symtoms (get lymph tissue outside of lymph nodes)
32
Non-Hodgkins disease is most common in ______ & the spread is
older adults alot less predicable & prognosis is less certain
33
What makes Non-Hodgkins disease difficult to treat?
majority of pts have widely spread disease at time
34
Clinical manifestations of Non-Hodgkins disease
Painless lymph node enlargement & non-specific symptoms (fever, night sweats, wt loss)
35
Treatment of Non-Hodgkins disease
-Chemotherapy -Radiation -Refractory cases: stem cell transplants -Rituximab, ibritumomab tiuextan, tositumomab
36
What is the typical location of Hodgkins disease
Cervical
37
What is Multiple Myeloma?
-Cancer of B cells -Atypical proliferation of one of immunoglobulins " M protein": a monoclonal antibody (increased osteoclasts, lead to bone destruction) -Unable to maintain humoral immunity (antibody secretion)
38
Multiple Myeloma is characterized by
-bone pain/fractures, also symptoms r/t impaired production of RBC & WBC
39
Who is most at risk for Multiple Myeloma?
African American Men Age 65
40
Clinical manifestations of Multiple Myeloma
Slow and insidious, skeletal pain, hypercalcemia
41
Diagnostics of Multiple Myeloma
-Monoclonal antibody protein in serum & urine -Pancytopenia (Every WBC & RBC decreased) -Hypercalcemia -Bence Jones protein in urine -Elevated serum creatinine (decreased kidney function) -X-rays osteolytic lesions