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20 Cards in this Set

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Middle aged, 40-60
Painless, generalized lymphadenopathy
Germinal center B cells
CD19, CD20, CD10+
t(14;18)
Follicular Lymphoma (FL)
Prognosis?
Indolent but incurable.
40% transform to Diffuse Large B-Cell Lymphoma, death within 1 year.
Median age 60, but wide range
B-Symptoms common (fever, weight loss, night sweats)
Diffuse, large (4-5x normal) cells
Diffuse Large B-Cell Lymphoma
Prognosis?
Fatal if untreated.
Chemo 75% remission, 35% cured.
>50 years old
lymphocytosis
later, cytopenia
smudge cells in PB
diffuse effacement of nodal architecture, with homogeneous small round lymphocytes
CD19, CD20, CD23, CD5
Chronic Lymphocytic Leukemia (CLL)
Small Lymphocytic Lymphoma
Prognosis?
Indolent, incurable
Survival 4-6 years
pancytopenia -> infections, bleeding
transform to Prolymphocytic leukemia (20%)
transform to Diffuse Large B-cell Lymphoma (10%)
mature looking lymphocytes in stomach
H.pylori infection
extranodal Marginal Zone Lymphoma (MALToma)
Prognosis?
Cured by killing H. pylori
starry sky pattern cells
EBV
Burkitt Lymphoma
African (endemic) presentation?
Sporadic presentation?
Endemic: Mandible
Sporadic: Iliocecal
c-myc oncogene on chromosome 8
CD19, CD20, CD10, surface Ig
t(8;14)
Burkitt Lymphoma
Prognosis?
Virus?
Extraordinarily aggressive
Usually cured with high dose chemo.
EBV
middle aged male
pancytopenia, splenomegaly
PB: pale blue cytoplasm with thread or bleb-like extensions
BM: dry tap
Spleen: beefy red appearance
CD11c, CD20, CD25, CD103
Hairy Cell Leukemia
Prognosis?
Easily cured.
>50 years old, male
bone pain
cytopenia
organomegaly
renal insufficiency secondary to hypercalcemia, Bence Jones proteins, amyloid deposition
Multiple Myeloma
Prognosis?
Untreated, death in 1 year.
Alkylating chemo - 3 years.
if <50 yo, bone marrow transplant - 10 years
Multiple Myeloma
Diagnostic Criteria
M-protein in serum or urine
Bone marrow clonal plasma cells or plasmacytoma
Organ or Tissue Impairment - what is CRAB?
Calcemia (hyper)
Renal Insufficiency
Anemia
Bone Lesions
Painless rubbery large lymph nodes
Pain in lymph nodes post EtOH
Fever, night sweats, weight loss
Reed-Sternberg cells
Hodgkins Lymphoma (HL)
What is Ann Arbor staging?
I single lymph node (LN) region
II 2 or more LN regions on same side of diaphragm
III LN regions on both sides of diaphragm, which could include spleen
IV Multiple / disseminated involvement of 1 or more extralymphatic organs or tissues (including bone marrow)
Reed-Sternberg (RS) cells
CD15, CD30
Hodgkin's Lymphoma
Classical type
what are subtypes?
Nodular sclerosis 65%
Mixed cellularity 25%
Lympocyte depleted <5%
Lymphocyte rich - very uncommon
Reed-Sternberg (RS) cells
CD20, CD45
Hodgkin's Lymphoma
Variant type
what is the subtype?
Lymphocyte predominant 5%
young adult
Enlarged mediastinal lymph nodes.
Histo: Lymph node has large nodules surrounded by thick fibrous collagen bands.
Reed-Sternberg (RS) cells
Classical Hodgkin's
Nodular Sclerosis
Reed-Sternberg (RS) cells
EBV
Biphasic - young adults & adults > 55
Classical Hodgkin's
Mixed Cellularity
Reed-Sternberg (RS) cells
EBV
RS cells are bizarre
Elderly or HIV+
Classical Hodgkin's
Lymphocyte Depleted
<35 yo
Cervical or axillary nodes
Reed-Sternberg (RS) cells
EBV negative
RS cells are "popcorn" cells
Variant Hodgkin's Lymphoma
Lymphocyte predominant
Prognois?
Indolent but tend to recur.
<5% transform to non-Hodgkin's large B-cell lymphoma
Hodgkin's Lymphoma
Treatment and Prognosis
Stage is most important prognostic indicator.
5 year survival:
Stage I-II: 90%
Stage IV: 60-70%
What is side effect of therapy?
Long term survivors get secondary cancers (AML, LungCA) due to drugs.
Abrupt and severe onset -> Flu that won't stop.
Cytopenia
Enlargement of LNs, liver, spleen
Thymic enlargement
TdT+, CD2, CD7
NOTCH1 mutation
Precursor T-cell
Acute Lymphoblastic leukemia/lymphoma
Prognosis?
No prediction.
Abrupt and severe onset -> Flu that won't stop.
Cytopenia
Enlargement of LNs, liver, spleen
Testicular enlargement
CNS involvement
TdT+, CD19
Precursor B-cell
Acute Lymphoblastic leukemia/lymphoma
Good Prognosis:
Age: 2-10 years
WBC in PB: low
Pre-B type
hyperploidy (>50 chromosomes)
t(12;21)
All others die within months.
What are the good and bad translocations in ALL?
Good: t(12;21)
Bad: t(9;22)