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44 Cards in this Set
- Front
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Acute myelomonocytic leukemia |
Aka M4. This leukemia is characterized by the differentiation along both myeloid and monocytic lines. Monocytes and promyelocytes represent >20%, <80% of the bone marrow differential. |
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When stained, more than 20% should be positive for what? |
MPO and NSE |
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What level is increased 3 times with M4? |
Serum lysozyme. |
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Specific markers for myelomonocytic cells |
CD13 and CD33 |
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Chromosomal transference associated with M4 |
4:11, 9:11. |
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What is seen on peripheral smear with M4? |
Monocytosis. |
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M4e |
Variant of M4. It is M4 with moderate eosinophilia. >5%. |
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What chromosome is M4e associated with? |
Inversion of chromosome 16. |
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M5 |
Acute monocytic leukemia. Two subtypes. M5a and M5b. |
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M5a |
Cells are poorly differentiated. |
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M5b |
Shows differentiation. Most cells are recognizable promonocytes and monocytes. |
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Cells associated with M5b |
More mature cells. 80% are monoblasts, promonocytes, and monocytes. |
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Cells associated with M5a and chromosomal transference |
9:11. 80% monoblasts. |
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C14 is found almost exclusively on which cells? |
Monocytes. |
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M6 |
Aka acute erythroblastic leukemia or Di Guglielmo's Syndrome. Only one in which there is hyperplasia of both the myeloid and erythroid cells. Rare and difficult to diagnose. |
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Nucleated marrow cells associated with M6 |
More than 50% of the Nucleated marrow cells are abnormal nucleated red blood cells. (30% considered adequate by some) |
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Morphology of M6 |
The leukemic red cells are frequently bizarre with extreme dysplastic features including: giant forms, multinucleation, cytoplasmic vacuolization, cytoplasmic buds, and megaloblastoid changes, ringed sideroblasts. |
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Anemia with M6 is due to: |
Increase of undifferentiated erythroblasts. |
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M7 |
Acute megakaryotic leukemia. Rarest of AMLs constituting less than 1% of all cases. |
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What disorder do patients with M7 usually have? |
A preceding myeloproliferative disorder. |
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M7 in children |
Seen more frequently in patients less than 3 years of age and with Down's syndrome. |
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Cytoplasm of M7 and why do blasts clump together? Translocation between which 2 chromosomes? |
Granular. Blasts will clump together due to protein change. (1;22) |
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Eosinophilic leukemia |
Rare variant of acute myeloid leukemia in which blasts and immature eosinophils proliferate. CNS involvement appears to be common. Should be distinguished from CML with large numbers of eosinophils. |
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Basophilic leukemia |
Rare subset of AML associated with t(6:9) and abnormal 12p. Ultra structure studies of the immature basophilic granules may be necessary. |
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Philadelphia chromosome |
Associated with basophilic Leukemias. Positive cases may be related to the blast crisis of CML. |
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Extramedullary myeloid cell tumor and other names |
Aka granulocytic sarcoma or chloroma is in an extra medullary tissue mass of blasts and immature myeloid cells. |
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Color of EMCT and what does it represent? |
Turns green upon exposure to the air as large amounts of peroxidase are oxidized. May represent the initial manifestation of acute leukemia or signal relapse. |
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Blast crisis of CML may represent: |
EMCT. |
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Masses of monoblasts may be seen with: |
M5 Leukemias and sometimes referred to as EMCT. |
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Blast crisis of chronic leukemia |
Refers to phase of chronic leukemia resembling an acute leukemia in which blasts are more than 30%. In CML, blast crisis signals the terminal phase of the disease for which there is no effective therapy. |
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Secondary therapy induced acute leukemia |
Nearly always myeloid and is usually preceded by myelodysplastic syndrome involving all three hematopoietic cell lines. (Panmyelosis) |
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Abnormalities of chromosomes with secondary acute leukemia and when is it most common? |
5, 7, and 11 are common. This is most common after alkylating chemotherapy or radiation therapy, with an average latent period of 5 years. |
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Hypocellular acute leukemia |
Situation in which marrow cellularity (<30%) often resembles aplastic anemia, but with numerous (30%) blasts in the interstitium of the marrow. About 5-10% of acute myeloid Leukemias present in this form. |
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Classification of acute lymphoblastic leukemia |
L-1: 85% L-2: 14% L3: Burkitt's 1% childhood |
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What ages do most lymphoblastic Leukemias occur? |
2-10. Good prognosis. 90% go into remission. 60% completely cured. |
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L1 |
Aka acute lymphoblastic leukemia. Most common ALL found in children and appears to have best prognosis. |
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Morphology of L1: cells, chromatin, and nuclei |
L1 blasts are small (about twice the size of small lymphocyte) and homogeneous (easier to kill). Chromatin is usually finely dispersed. Nuclei are round and regular with the clefting and inconspicuous nucleoli. Cytoplasm is scanty. |
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Which cell line is lymphocytic leukemia typically associated with? |
B cells. |
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L2 |
Acute lymphoblastic leukemia. Most frequent ALL found in adults. Blasts demonstrate marked heterogeneity. Great deal of variability in each case. |
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Morphology of M2 |
Blasts are large and heterogeneous. Nuclei are irregular and often clefted (butt cells). One or more large nucleoli present. Volume of cytoplasm is variable, but abundant and may contain vacuoles. |
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Cell lineage of L2 |
B, but some t. |
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L3 |
Aka Burkitt's leukemia. Occurs in children and adults. Lymphoblasts similar to appearance to those found in Burkitt's lymphoma. Blasts are homogeneous. Large cells with abundant basophilic cytoplasm. Prominent cytoplasmic vacuolization. |
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Morphology of L3 |
L3 blasts are moderate large in size and homogenous. Nuclei are regular and round oval in shape. One more more prominent nucleoli. Volume of cytoplasm is moderate and contains prominent vacuoles. |
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Chromosomal abnomalities of L3 |
t(8;14), t(2;8), t(8;22) |