Exam 2 - chapter 24 Flashcards

1
Q

hodgkin lymphoma

A

Malignant b cells invade lymphoid organs
Adults 20-40 years
Spreads from lymph node to lymph node and then to organs via lymphatic system
Defective b-lymphocytes → reed sternberg cells (larger, multinuclei, abnormal shape)

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2
Q

Stages hodgkin lymphoma

A

1: 1 lymph node involved
Stage 2: 2+ lymph nodes in same region on the same side of the diaphragm (thoracic region)
Stage 3: lymph nodes on both sides of diaphragm
Stage 4: spread outside of lymphatic system
Internal organs, liver, bones, spleen etc
Sooner you catch it, better prognosis, can be eradicated if caught ear

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3
Q

Non hodgkin lymphoma

A

Multiple lymph node involvement scattered throughout the body at diagnosis
Wide spread metastases at diagnosis
More difficult to treat
Can either be b cell or cell lymphoma
Indolent vs aggressive
No reed sternberg cells
Treatment: radiation, chemotherapy, prognosis (localized is better if caught early)

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4
Q

Acute leukemia

A

Young age of onset
Myelogenous or lymphoid cells that are affected cause disease
Comes on fast and is severe
Responds better to treatment
Better prognosis
More undifferentiated cells

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5
Q

Chronic leukemia

A

Older age of onset
Myelogenous or lymphoid cells that are affect cause disease
Less severe, comes on slower
Responds worse to treatment
Worse prognosis
More differentiated and mature cells

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6
Q

What is the most common type of leukemia seen in children, seen in adults

A

Children: acute lymphotic leukemia (ALL)
Adult: acute myelogenous leukemia (AML), chronic lymphotic leukemia (CLL)

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7
Q

Treatment leukemia

A

chemo and bone marrow transplant

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8
Q

Philadelphia chromosome

A

Translocation or splitting and sharing of material between chromosome 9 and 22. Chromosome 22 has a piece of 9 on it, results in CML

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9
Q

Know what cells give rise to myelogenous and lymphocytic leukemia

A

Acute lymphocytic leukemia*: B or T lymphocytes
Acute myelogenous leukemia#: granulocytes
Acute monocytic leukemia: monocytes
Chronic lymphocytic leukemia: B lymphocytes#
Chronic myelogenous leukemia: granulocytes

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10
Q

most common type of Hodgkin lymphoma

A

Nodular sclerosis Hodgkin lymphoma- most common
develops in teens and young adults 15–35 years of age

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11
Q

CML

A

(10-15% of all leukemias - philadelphia’s chromosome)
Diagnosed in older ppl, avg 67 yo
Excessive production of granulocytes, erythroid precurses and megakaryocytes
3 phases

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12
Q

Chronic phase of variable length CML

A

Onset sloe with non specific symptoms like weakness, weight loss
leukocytosis , anemia, thrombocytopenia

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13
Q

Accelerated phase
CML

A

Enlarged spleen and progressive symptoms
Increases basophils count and more immature cells in blood/bone marrow
Low grade fever, night sweats, bone pain(rapid division of cells in bone marrow), proliferation of leukemic cells

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14
Q

Terminal blast crisis phase (3 mo to live)

A

Evolution to acute leukemia and is characterized by an increase number of immature myeloid precurse cells especially blast cells
Symptoms: shortness of breath, dyspnea, lethargy, headache, bleeding from gums
Poor prognosis, increased risk of infection

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15
Q

CLL

A

33%
B lymphotcytes
Aggerssive form, less aggressive form
Diagnosed in older population 72 yo avg
Rarely seen in people under 40
Hypogammaglobulinemia - increased infection

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16
Q

mononucleosis

A

Caused by Epstein bar virus, spread via contact with oral secretions (b cells)
Atypical, enlarged, lymphocytes
Heterophil antibody produced by infected B cells and reacts with antigens from another species (ie sheep RBC)
Hepatitis and splenomegaly
Nausia, anorexia, hepatomegaly and jaundice
Overall increase in WBC

17
Q

multiple myeloma

A

Abnormal B cells
Idiopathic
Occurring in adults and involves plasma cells  what are plasma cells?
Proliferation/activation of osteoclasts
Break down bone
Plasma cells collect in bone causing multiple tumors with erosion of bone
Impaired blood cell formation, impaired antibody production
Hypercalcemia

18
Q

multiple myeloma s/s

A

Frequent infections
Bone pain
Multiple Fractures
Anemia
Kidney function - proteinuria and renal failure

19
Q

multiple myeloma Diagnosis

A

M proteins, bone pain, increased plasma cells in blood, >10% plasma cells in bone marrow

20
Q

multiple myeloma Treatment

A

Chemotherapy
thalidomide
Analgesics for bone pain
Blood transfusion
Treatment for kidney problems
Kidney and bone marrow transplant