Lukemia Flashcards

1
Q

Myelogenous Leukemia

A

Leukemia characterized by proliferation of myeloid tissue (as of the bone marrow and spleen) and an abnormal increase in the number of granulocytes, myelocytes, and myeloblasts in the circulating blood

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2
Q

Development of Leukemia in the Bloodstream

A
Stage 1- Normal
Stage 2- Symptoms
Stage 3- Diagnosis
Stage 4- Worsening
Stage 5a- Anemia
Stage 5b- Infection
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3
Q

Acute myeloid leukemia (AML) Etiology

A

Genetic damage to the DNA of a single cell in the bone marrow that primarily affects older people.

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4
Q

Acute myeloid leukemia (AML)

A

cancer of the blood-forming tissue (bone marrow).

causes bone marrow to produce too many immature white blood cells (blast cells).
Suppresses normal blood cell production.
…leads to Anemia, leukopenia, thrombocytopenia

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5
Q

Acute Myeloid Leukemia (AML) Physical Findings

A
Fever (unexplained for >3 weeks)
Multiple bruises
Unexplained infections
Bleeding/bruising/petechiae (gingivae, GI bleed)
Splenomegaly
Sternal tenderness
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6
Q

Treatments for AML

A
Chemotherapy
	Phase One – Induction therapy
	Phase Two – Intensification therapy
	Phase Three – Maintenance
Radiation therapy for certain cases
Bone marrow transplantation
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7
Q

Acute Lymphoid Leukemia (ALL) Incidence

A

Mostly affects children, accounts for 3/4 of childhood leukemia (peak age 4 years)

Comprises less than 30% of leukemia in young adults

May be B-cell, T-cell, or null-type (non-B, non-T cell)

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8
Q

Acute Myeloid Leukemia (AML) Presenting Symptoms

A
Fatigue
Shortness of breath on exertion
Easy bruising
Bleeding in the nose or from the gums
Prolonged bleeding from minor cuts
Recurrent minor infections or poor healing of minor cuts
Loss of appetite or weight loss
Mild fever

Symptoms usually present for 3 or more months before diagnosis is made

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9
Q

ALL Common Sx with children:

A
Fever
Bleeding
Easy bruising
Petechiae
Bone pain
Fatigue
Shortness of breath
Weight loss / failure to thrive
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10
Q

Acute Lymphoid Leukemia (ALL)

A

Clonal proliferation and accumulation of blast cells in blood, bone marrow and other organs

Disorder originates in single B or T lymphocyte progenitor

Heterogenous disease with different biological subtypes

Incidence in adults : 20% of acute leukemias
Etiology - unknown

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11
Q

Acute Lymphoid Leukemia (ALL) Hematological Findings

A

Anemia (normochromic, normocytic)

WBC < 5,000 (or > 25,000)
Leukocytosis (median = 15,000)

Thrombocytopenia

Smear, Blast cells (< 50,000)

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12
Q

Immunologic classification of ALL

A

B- lineage (85%) Markers:
Typically is CD10+, CD19+, and sometimes CD20+

T-lineage (15%):
Positive for CDs 2, 3, 4, 5, 7, and 8.

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13
Q

Chronic Myeloid Leukemia (CML)

A

Proliferative disorder of hematopoietic stem cells

Well-characterized clinical course

Philadelphia (Ph) chromosome (Unique chromosomal abnormality)

Bcr-Abl tyrosine kinase: A single molecular abnormality that causes transformation of a hematopoietic progenitor into a malignant clone

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14
Q

Chronic Myeloid Leukemia (CML) Incidence

A

1-2 cases per 100,000 people/year

Higher among men than women

Median age of presentation is 50 yo

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15
Q

Chronic Myeloid Leukemia (CML) Clinical Features

A
40% asymptomatic
Chronic phase
Splenomegaly often massive (Increasing abdominal girth)
Features of anaemia
Abnormal platelet function (Bruising, epistaxis, menorrhagia)
Hyperleukocytosis 
Chronic infection
Fever
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16
Q

Chronic Lymphoid Leukemia (CLL)

A

Overall median survival is 10 years

Individual prognosis is highly variable

Clinical staging systems:
Mainstay of assessing prognosis
Only requires examination and blood count
Used to determine when to start therapy

17
Q

Chronic Lymphoid Leukemia (CLL) Incidence

A

4-7 new cases per 100,000 people per year

Comprises 30% of all cases of leukemia

Most common lymphoid leukemia

18
Q

Chronic Lymphoid Leukemia (CLL) Common Symptoms

A
Note: approximately 25% of patients are asymptomatic at the time of diagnosis
 Fever 
 Night sweats 
 Fatigue
 Pallor
 Shortness of breath
 Easy bruising
 Gingival bleeding
 Weight loss
 Frequent infections
 Fever
 Splenomegaly and/or hepatomegaly
 Lymphadenopathy
19
Q

Rai Staging

A
  1. Lymphocytosis (>5 G/L)
    I. Lymphocytosis + lymphadenopathy

II.Lymphocytosis + splenomegaly +/-lymphadenopathy

III. Lymphocytosis + anemia (Hb <100G/L) +/- anemia +/-lymphadenopathy +/- splenomegaly

20
Q

Binet Staging

A

A. < 3 involved areas, Hb > 10g%, Plt > 100G/L
B. > 3 involved areas, Hb > 10g%, Plt > 100G/L
C. Any number of involved areas, Hb < 10g%, Plt < 100G/L

21
Q

Hairy Cell Leukemia

A

2% of all adult leukemias
Usually in males > 40 years old
Chronic disease of lymphoproliferation
B lymphocytes that infiltrate the bone marrow and liver

22
Q

Hairy Cell Leukemia Incidence

A

Rare
Men….55 yo
Decreased WBC’s/platelets

23
Q

Hairy Cell Leukemia Clinical Presentation

A

Splenomegaly
Pancytopenia
Infection
Vasculitis