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26 Cards in this Set

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Acute Lymphoblastic Leukemia (ALL) - definition
fast-growing cancer of a type of white blood cells called lymphocytes.
ALL is most common in?
* children
* Most common malignancy in children
Risk factor for ALL in children?
Smoking around them
Common features of ALL/AML/CLL?
* Ill for only a few days or weeks.

* Bleeding may occur in skin/mucosal surfaces/gingival surfaces/epitaxis/menorrhagia

* Increased risk of infection

* Gum hypertrophy or bone/joint pain
Increased risk of infection in ALL/AML/CLL may present as? from?
* E. Coli, K. pseudo, or fungi

* presenting as rapid life threatening cellulitis, perirectal infection or pneumonia
ALL/AML - PE?
* Pallor, Purpura and petechiae

* Variable enlargement of liver, spleen and lymph nodes

* Possible bone tenderness in sternum, tibia and femur
Hallmark of ALL?
pan cytopenia with circulating blasts
Lab findings in ALL?
* Hallmark: Pan cytopenia w/ circulating blasts

* Mediastinal Mass on CXR

* Anemia and thrombocytopenia w/o reticulocytosis

* Aleukemic is always acute
Acute Myeloid Leukemia (AML)
cancer that starts inside bone marrow. Cancer grows from cells that normally turn into white blood cells.
AML is most common in?
* Adults
* Most common leukemia in adults
Lab findings AML?
* Hallmark= pan cytopenia with circulating blasts

* Auer rods pathognomic for AML

* Packed marrow: dry tap

*
Chronic Lymphocytic Leukemia
• “Small Cleaved Lymphoma” same disease at different stages.

• Clonal malignancy of B cells
Chronic Lymphocytic Leukemia is MC in?
• middle aged adults (50’s and 70’s)
CLL - Hallmark?
isolated lymphocytosis Co expression of CD19 and CD5
What cell type is common in CLL?
Smudge Cells
Definition of "B symptoms"?
weakness, night sweats, weight loss, repeated infections, symptomatic anemia
CLL - PE?
* abdominal fullness caused by splenomegaly
* common findings of AML/ALL/CLL
* "B symptoms"
* symptoms of CLL develop gradually
* Rare: blurred visions, respiratory distress,
Laboratory Hallmark findings in CLL?
* isolated lymphocytosis, with a leukocytosis of greater than 20,000 cells/mL

* leukocytosis, with a median WBC count of 150,000 cells/mL.

* large granular lymphocyctic syndrome (B-type)

* Philadelphia chromosome
Treatment is withheld/given under what conditions for CLL?
Treat if have B symptoms but if ("A symptoms") not can just observe
Chronic Myeloid Leukemia - Def?
myeloproliferative disorder that starts inside bone marrow. Overproduction of myeloid cells
What is the avg age of onset for CML?
* Median age onset is 67 years old
What is a hallmark of CML?
Philadelphia chromosome: BCR/ABL gene codes for Tyrosine Kinase that induces unregulated production of mature myeloid cells
What are the three phases of CML?
1) chronic
2) accelerated
3) acute (blast crisis, defined as 30% blast cells in the blood or bone marrow).

* inevitably becomes acute.
CML - PE
• Spleen is enlarged
• Sternal tenderness may be present
• Often asymptomatic
Lab Findings of CML
• Elevated WBC- 150,000/mcl
• Normal hematocrit, RBC normal, (-) anemic
• Platelet normal/elevated
• Presence of bcr/oabl gene detected by PCR test= hallmark aka Philadelphia chromosome
CML - Tx
Tyrosine Kinase Inhibitors: Dasatinib – Sprycel *** drug of choice