Chapter 11: Disorders of WBC and Lymphoid Tissues Flashcards

1
Q

What is leukopenia?

A

abnormally low number of WBC in the blood

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2
Q

What is granulocytopenia?

A

abnormally low concentration of granulocytes in the blood

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3
Q

What is aplastic anemia?

A

deficiency in bone marrow maturation of all cell types from stem cells

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4
Q

What is neutropenia?

A

Low number of neutrophils

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5
Q

What is agranulocytosis?

A

it is a state of virtually no neutrophils

techinically a type of neutropenia

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6
Q

List 4 causes of neutropenia.

A

1) acquired (drug, infection related)
2) congenital
3) neoplasms
4) autoimmune

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7
Q

Describe what infectious mononucleosis is.

A

a self-limiting lymphoproliferative disorder that lasts 2-3 weeks

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8
Q

What virus causes infectious mononucleosis?

A

the Epstein-barr virus

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9
Q

What age groups is infectious mononucleosis more common in?

A

adolescents and young adults

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10
Q

Describe the pathogenesis of infectious mononucleosis.

A

the virus penetrates the nasopharyngeal, oropharyngeal, and salivary lymphocytes into the lymphoid tissue.

It then binds to B cells and either kill it or incorporate itself into its genome.

If incorporated, circulates and secretes a hetorophil (antibody that reacts with antigens from other species) which can be traced to diagnose.

Once infection is over, some b-cells remain in the mouth and occasionally shed into saliva to transmit. Inc shedding when immune system is suppressed

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11
Q

What type of cells are most important in regulating mono?

A

T cells and natural killer cells

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12
Q

Describe the common manifestations of mono.

A

1) begins insidiously (4-8 wk incubation)
2) initial malaise, anorexia, and chills
3) pharyngitis, fever, lymphedema
4) hepatitis (liver inflammation) and spenomegaly are common
5) rarely (more in adult) cranial nerve palsies (disruption of nerve function)

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13
Q

What are some complications that can occur as a result of mono?

A

ENCEPHALITIS: inflammation of the brain

MENINGITIS: infection of the brain

GUILLAIN-BARRE SYNDROME: immune system attacks peripheral nervous system

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14
Q

Describe leukemia.

A

malignant neoplasms of cells originally derived from hematopoietic precursor cells.

replaces bone marrow and results in highly immature and large numbers of WBC

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15
Q

List some causes of leukemia.

A

Largely unknown, but….

1) radiation exposure
2) benzene
3) antitumour drugs
4) post chemotherapy
5) genetic predisposition

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16
Q

What are 2 conditions that give you a genetic predisposition for leukemia?

A

Down syndrome

Neurofibromatosis

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17
Q

How is mono treated?

A

mainly symptomatic treatment.

bed rest
Tylenol for soar throat, headaches and fever

18
Q

How is leukemia classified?

A

either acute or chronic

and either myelocytic (myeloid stem line) or lymphocytic (lymphoid stem line)

19
Q

Describe the manifestations and characteristics of acute leukemia.

A

1) sudden onset
2) low grade fever, night sweats, weight loss
3) bone pain/tenderness
4) lymphadenopathy (swollen or enlarged lymph nodes)
5) symptoms of depressed bone marrow: WBC=infections, RBC=fatigue, thrombocytopenia=bleeding/bruisingng
6) leukostasis (inc number of circulating leukemic blast cells)
7) hyperuricemia (uric acid accumulation d/t cell breakdown

20
Q

what type of leukemia accounts for 1/3 of all leukemias?

A

chronic lymphocytic leukemia

21
Q

What is the biggest difference between chronic and acute leukemia?

A

Chronic is a proliferation of more fully differentiated cells than acute is.

Chronic is much more common in older adults

22
Q

What happens to the other stem cell line when there is a leukemia of the other?

A

its production is suppressed by the overproduction of the other

23
Q

What chromosome is affected in chronic myelogenous leukemia?

A

the Philadelphia Chromosome

24
Q

What are the three phases of chronic myelogenous leukemia?

A

CHRONIC

SHORT ACCELERATED

TERMINAL

25
Describe the symptoms of the chronic phase of chronic myelogenous leukemia
non specific symptoms: weakness, weight loss, anemia, thrombocytopenia
26
Describe the symptoms of the short accelerated phase of chronic myelogenous leukemia.
Splenomegally Low-grade fever Night sweats Bone pain
27
Describe the terminal phase of chronic myelogenous leukemia.
Evolves to acute leukemia the Ca spreads and infiltrates the skin, lymph nodes, bones, and CNS
28
What type of cell does chronic lymphocytic leukemia most impact?
B-cells it is called a B lymphocyte malignancy
29
Describe the progression and manifestations of chronic lymphocytic leukemia.
Can have minimal symptoms or be rapid and fatal manifestations: - elevated lymphocytes - lymphoedema - hepatosplenomegaly - hypogammaglobulinemia (dec antibodies)
30
Describe treatment for chronic lymphocytic leukemia
chemotherapy radiation stem cell transplant
31
Describe the cause of non-Hodgkin lymphoma
relatively unknown but related to impaired immune system and infectious agents
32
Describe the spread of non-Hodgkin lymphoma (NHL)
can originate in an of the lymphoid tissues, commonly originate in the nodes. spreads unpredictably to the liver, lymphatic tissues, spleen, and bone marrow
33
Describe the manifestations of non-Hodgkin lymphoma (NHL)
depend mainly on the type slow growing painless lymphadenopathy, many eventually transform into more aggressive forms of lymphoma or leukemia fever, sweating, weight loss, susceptibility to infections
34
Describe treatment of Non-Hodgkin lymphoma.
localized radiation or combined with chemotherapy
35
What may be a cause of Hodgkin lymphoma (HL)
previous exposure to infectious mononucleosis
36
What type of cell must be present to indicate Hodgkin lymphoma (HL)
Reed-Sternberg cell
37
Compare how Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL) originate.
NHL: frequently arises in extranodal cites and spreads to anatomically contiguous nodes HL: originates in a single node or chain of nodes
38
Describe the manifestations hodgkins lymphoma (HL)
lymph node enlargement above the diaphragm night sweats, pruritis, fever, chills, wt loss, fatigue, anemia
39
Describe the treatment of Hodgkin lymphoma.
begins with staging then: radiation and chemotherapy
40
What is multiple myeloma? describe the process.
it is a plasma cell dyscrasia proliferation of a single type of malignant plasma cells. Main sites are bone and marrows. Results in abnormal proliferation of marrow plasma cells and activation of osteoclasts.
41
What are some manifestations of multiple myeloma?
Pathologic fractures with hypercalcemia bone pain hyper-viscosity of body fluids d/t release of protein from bone heart failure/nephropathy (d/t debris and viscosity) myeloma nephrosis (from filtering) Bacterial infections Plasma cell tumors symptoms of bone marrow suppression
42
Describe the treatment options for multiple myeloma
Medications high dose chemo and stem cell transplant