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
Q

Describe the genetic link of leukemia

A

high rates among those with genetic abnormalities (10x normal rate in Down Syndrome)

26
Q

What is acute leukemia

A

Sudden onset, >30% blast cells = diagnostic

27
Q

What is the MC childhood cancer?

A

ALL- acute lymphocytic leukemia

28
Q

What is the signs and symptoms of acute leukemia

A

S/Sx related to bone marrow depression, fever, fatigue, pallor, wt loss, infection, bruising, nosebleeds, CNS in ALL than AML

29
Q

Who is affected by AML?

A

mostly adults, linear increase thru middle age

30
Q

What are signs of pan-cythemia

A

dont clot, anemic, red cells don’t work

31
Q

What is chronic leukemia

A

Well differentiated myeloid and lymphoid cells

32
Q

What is the pathogenesis of CLL

A

CLL - mostly > 50; Malignant transformation of *B cells, Cells immunologically incompetent and Pt gets lots of Infections with Autoimmune activity

33
Q

What is the pathogenesis of CML

A

CML - 30-50yo. Transformation of pluripotent stem cell, has a characteristic Philadelphia Chromosome which is Chromosome 9:Chromosome 22 translocation

34
Q

What is the characteristic of multiple myeloma?

A

Bence Jones protein. Calcium R A B.

35
Q

What is the presentation of CLL

A

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
Q

What is the presentation of CML

A

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
Q

What is neutropenia associated with leukemia

A

Occurs rapidly because of 1d life span in blood and then Move into peripheral tissue