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79 Cards in this Set

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  • Back
What will cause a False INCREASE in WBC? (4)
unlysed/nucleated RBC
Platelet cumpling
Monoclonal proteins, cryfibrinogen, cryoglobulin
Heparin
What will casue a False DECREASE in WBC? (2)
Smudge cell
Clotting
Uremia + Immunosuppressant
50 year olds BM cellularity
50%
CD45 antigen
Every leukocyte aka all of them
CD 3, 5, 4, and 8
T cell antigens
CD 19, 21, 10, and 20
B cell antigens
CD 34
Stem cell and progenitor cells
Most common malignancy of childern and adolescents
Acute Lymphoblastic Leukemia/lymphoma (ALL)
Most common Adult leukemia
Chronic Lymphocytic Leukemia (CLL)
Most common INDOLENT Non-Hodgkin Lymphoma
Follicular Lymphoma
Most common Non-Hodgkin lymphoma overall
Diffuse Large B-Cell Lymphoma
Positive for TdT (terminal deoxynucleotidyltransferase)
Acute Lymphoblastic Leukemia/Lymphoma (ALL)
Smudge cells
CD 5 +
CD 19 +
CD 20 +
Chromic Lymphocytic Leukemia
BCL2 +
Follicular Lymphoma
What chromosome is involved in BCL2 gene? What lymphoma is this associated with?
t(14;18)
Follicular Lymphoma
Spreads via Lymphomatoid polyposis
CD 5 +
DI expressed
Mantle Cell Lymphoma
What are the key features of Marginal Zone Lymphoma? (3)
Found in tissues involved in inflammation/infection
Remains localized for long time
Regress if you get rid of the agent
Huge B-cell that can fit about 4-5 other cells within it
Diffuse Large B-cell Lymphoma
Immunodeficiency-associated Ig B-cell Lymphoma
Body Cavity Ig cell Lymphoma
Are subtypes of what Lymphoma?
Diffuse Large B-cell Lymphoma
Diffuse Large B-cell lymphoma subtype associated with:
T-cell immunodeficiency w/
Neoplastic B cells infected w/ Epstein-Barr virus
Immunodeficiency-associated Ig B-cell Lymphoma
Diffuse Large B-cell Lymphoma subtype associated with:
HIV or elderly patients w/
tumor cells associated with KSHV/HHV8
Body Cavity Ig cell Lymphoma (Primary effusion lymphoma)
Burkitt Lymphoma
Just know that it exists
Maltoma: mucosa-associated-lymphoid-tumors
Marginal Zone Lymphoma
Which type of immature cell is most common in childern <3 and which is in Teenagers for ALL?
< 3: Pre-B cells
Teenagers: Pre-T cells
Pre-T cells in ALL is associated with
Mediastinal masses from the involvement of Thymus
What makes the prognosis of ALL worse?
< 2 years old
Presence in adulthood/teenager
Periperheral blood > 100, 000
Phila Chromosome t(9;22)
Chromosome t(9:22)
Phila chromosome
Acute Lympoblastic Lymphoma/Leukemia
What is Leukocytosis?
Increase in WBC
What are the factors that affect peripheral leukocyte count? (4)
Size of pool
Rate leaving pool
Marginal pool
Extravasation rate from blood to tissues
Leukocytosis casued by Inflammation
Neutrophilic leukocytosis
Drug toxicity most commonly causes what?
Neutropenia (agranulocytosis)
Systemic fungal infection, parasitic infection causes
Eosinophilia
Caused by recovery from neutropenia, TB
Monocytosis
Caused by chronic hemolytic anemia, Myeloproliferative disease
Basophilia
Define Lymphocytopenia
Decrease in absolute lymphocytes
Caused by Rheumatoid arthritis/lupus
Plasmacytosis
CD 4
HTLB-1 infection
Adult T cell Leukemia/Lymphoma
Most common Sx: Bone pain
Multiple Myeloma
Most common serum monoclonal protein found in Multiple Myeloma
IgG
Sx: plasma cell dyscrasia
but patient presents as Asx with low serum M protein
MGUS
Monoclonal protein found in Waldenstrom Macroglobulinemia (hyperviscosity syndrome)
IgM
Rouleaux formation (due to Increasedd globin)
Multiple Myeloma
Lab: Increase Ig/Bence Jones Proteins (light chain) in blood and urine
Multiple Myeloma
EBV with hemophagocytic syndrome
Extranodal NK/T-cell Lymphoma
ALK gene
Horseshoe nucleus
Anaplastic Ig Cell Lymphoma
Felty Syndrome
Large Granular Leukemia/lymphoma
Rheumatoid arthritis
Large Spleen
Neutropenia
Felty Syndrome
CD 4
Skin lesions
Mycosis Fungoides
Sezary Syndrome
Reed Sternberg Cell (owl eyes) with non-neoplastic background
Hodgkin Lymphoma
What is the avg age Hodgkin Lymphoma is seen?
What is used to give the prognosis?
32 yrs old
Tumor Stage
Is the spread of Hodgkin Lymphoma predictable?
YES!
Spread pattern for Hodgkin Lymphoma
Nodal dz
Splenic dz
Liver dz
Marrow involvement
Extranodal dz
Lacunar cells within collagen is seen in which stage of Hodgkins Lymphoma
Nodal dz
CD 15 +
CD 30 +
EBV -/+
Classical HL
CD 15 -
CD 30 -
EBV -
Non-classical HL
Lymphocyte predominance
Non-classical HL
Localized to single node group
HL or Non-HL
HL
Multiple nodes involved
HL or Non-HL
Non-HL
Orderly spread
HL or Non-HL
HL
Non-continous spread
HL or Non-HL
Non-HL
Rarely involves mesenteric nodes and Waldeyer ring
HL or Non-HL
HL
Commonly involves Waldeyer ring and mesenteric nodes
HL or Non-HL
Non-HL
Rarely presents as Extra-nodal
HL or Non-HL
HL
Commonly presents as Extra-nodal
HL or Non-HL
Non-HL
Myloperoxidase
CD 13, 33, 117
CD 14, 64
Myeloid Antigens
Chromosome t(15;17)
Acute Myeloid Leukemia
Patient with AML is at high risk for...
DIC
What are the Major feartues of AML? (3)
M6 Acute erythroleukemia
> 50% erythroblasts
> 20 % myleblasts in nonerythroids
Which major feature Dx AML?
> 20% of myeloid blasts in bone marrow
GPIIb/IIIa of vWF
Acute Megakaryoblastic Leukemia
Most common AML in Down Syndrome
Acute Megakaryoblastic Leukemia
Peripheral blood cytopenia with NO organ enlargement
Myelodysplastic Syndrome
Refractory anemia with Ringed Sideroblasts
Classification of MDS
5q- Syndrome is associated with what syndrome?
Myelodysplastic Syndrome
BCR-ABL Fusion
Philedelphia Chromosome
Chronic Myeloid Leukemia
JAK2 point mutation (tyrosine kinase mutation)
Polycythemia Vera
Birbeck granules on EM
Langerhan Cells
What is a Thymoma?
Tumors of thymic epithelial cells
What is Thymic carcinoma?
Tumors that are cytologically malignant