Leukemia Flashcards

1
Q

What is neutropenia

A

lack of production/degradation- lack of white cells, granulocytes, Neutropenia < 1500 cells, Agranulocytosis < 200 cells

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2
Q

What is leukopenia

A

reduction in white cells, but not as specific as neutropenia, that refers to neutrophils,

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3
Q

What are the acquired disorders that cause leukopenia

A

MC**1] Drug related (chemo, abx, AED), 2] Devastating infection, 3] Splenomegaly, 4] Bone marrow dz

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4
Q

What is how infections can cause leukopenia

A

at different courses in illness, white count may change. May be high initially, but then immune system can’t keep up so it goes down.

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5
Q

What is Felty’s syndrome

A

RA variant, splenomegaly, low WBC count in RA Patient

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6
Q

List the bone marrow diseases that can cause leukopenia

A

1] Aplastic anemia (or pancytopenia), 2] Irradiation (BM depression), 3] Overgrowth of other precursors

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7
Q

What is a genetic disorder that causes neutropenia?

A

Periodic/Cyclic Neutropenia-every 21-30 d, lasts approx 10d cycles: 1] Serious or recurrent bacterial/fungal infections (MC = respiratory), 2] Necrotizing oral lesions 3] Skin/mucosal ulceration like Aphthous

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8
Q

What is the formation and maturation of WBCs

A

WBCs are formed and differentiate in the bone marrow and They travel to the lymphoid organs to mature and develop

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9
Q

What is neoplasms arising from bone marrow

A

cause leukemias or plasma cell dyscrasias and can spread to LN

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10
Q

What is neoplasms arising from lymph node

A

lymphomas-Solid, lymphoid tumors spread to the BM

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11
Q

What is the most MCC of cancer in the US?

A

Skin

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12
Q

What is the hallmark of Hodgkin Lymphoma

A

Reed-Sternberg cells-1] Binucleated cell, 2] Clear chromatin, 3] Owl eyes

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13
Q

What is the incidence rate of Hodgkin Lymphoma

A

1] Bimodal distribution w/ peaks in 20s and >50, 2] M:F = 1:1 early, M>F late

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14
Q

What is the etiology of Hodgkin lymphoma

A

Etiology unknown - suspected response to infection EBV

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15
Q

What is presentation of Hodgkin Lymphoma

A

1] Single, painless enlarged lymph node (or small group), **2] Typically superior to diaphragm (cervical/mediastinal), CONTIGUOUS 3] Fever, chills, night sweats, 4] Rapid progression of abnormal lymphocytes leads to infectious disease and “anergy”

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16
Q

What is the issue in Hodgkin lymphoma

A

they don’t fight infections well due to abnormal morphology & functionality

17
Q

What is NON Hodgkin Lymphoma

A

1] Heterogeneous d/t transformation of cells at any stage of B or T cell differentiation, 2] 3x more common than hodgkins, 3] Viral cause also postulated, but not sure.

18
Q

What is the presentation of NON Hodgkin Lymphoma

A

1] Presentation depends on type and stage of tumor, 2] MC presentation is painless, superficial lymphadenopathy, 3] NON CONTIGUOUS spread, 4] Frequent infections - viral common

19
Q

What is leukemia

A

Malignant neoplasms of hematopoietic stem cells that replace bone marrow with neoplastic cells

20
Q

What is the most common childhood cancer

A

Acute Leukemia, but effects more adults than kids

21
Q

What is the classification of leukemia

A

1] Lymphocytic: immature lymphocytes, 2] Myelogenous: granulocytes/monocytes

22
Q

What is myelocytic leukemia

A

1] Mutation of myeloid cell line, 2] Overproduction of abnormal monocytes or granulocytes, 3] Production of other cell types decreases

23
Q

What is lymphocytic leukemia

A

1] Mutation of lymphoid cell line, 2] Overproduction of abnormal immune cells, 3] Production of other cell types decreases

24
Q

List the environmental exposures associated with leukemia

A

1] Chemotherapy 2] Benzene 3] Radiation

25
Describe the genetic link of leukemia
high rates among those with genetic abnormalities (10x normal rate in Down Syndrome)
26
What is acute leukemia
Sudden onset, >30% blast cells = diagnostic
27
What is the MC childhood cancer?
ALL- acute lymphocytic leukemia
28
What is the signs and symptoms of acute leukemia
S/Sx related to bone marrow depression, fever, fatigue, pallor, wt loss, infection, bruising, nosebleeds, CNS in ALL than AML
29
Who is affected by AML?
mostly adults, linear increase thru middle age
30
What are signs of pan-cythemia
dont clot, anemic, red cells don't work
31
What is chronic leukemia
Well differentiated myeloid and lymphoid cells
32
What is the pathogenesis of CLL
CLL - mostly > 50; Malignant transformation of *B cells, Cells immunologically incompetent and Pt gets lots of Infections with Autoimmune activity
33
What is the pathogenesis of CML
CML - 30-50yo. Transformation of pluripotent stem cell, has a characteristic Philadelphia Chromosome which is Chromosome 9:Chromosome 22 translocation
34
What is the characteristic of multiple myeloma?
Bence Jones protein. Calcium R A B.
35
What is the presentation of CLL
1] Slow, indolent course, 2] Often asymptomatic at dx, 3] Lymphocytosis on CBC, 4] Fatigue, reduced exercise tolerance, enlarged nodes, splenomegaly, 5] Usually an incidental finding
36
What is the presentation of CML
1] Variable chronic phase - slow onset with weakness/wt loss, 2] Short accelerated phase - spleen enlargement, constitutional signs, 3] Terminal blast crisis - evolution to acute leukemia (3 mo)= DEATH
37
What is neutropenia associated with leukemia
Occurs rapidly because of 1d life span in blood and then Move into peripheral tissue