• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/34

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

34 Cards in this Set

  • Front
  • Back
What do the following Translocations express? Which cancer?
----
t(15,17)
PML-RAR

APML (AML)
t(14,18)
BCl2

follicular
t(8,14)
C-myc

Burkitt’s
t(11,14)
Cyclin D

Mantle cell lymphoma
t(9,22)
Philadelphia -- BCR-ABL (tyr K)

CML (chronic myelogenous leukemia)
Jak 2 mt
All myeloproliferative Disorders (CML; PV, ET, Myelofibrosis)
Where do you see the following smears?
---
Auer rods
AML
Smudge Cells
CLL/SLL
Hairy Cytoplasm
Hairy Cell leukemia
RS cells
HL
Sezary Bodies
Mycosis Fungoides
Starry sky
Burkitt’s lymphoma
Tear Drop cell
Myelofibrosis
For the following give me Clinical Features, Prognosis, Tx
----
AML
MPO+ (Auer rods)
CD33, 13+
Superficial infiltration (gums, skin)

Good:
inv (16)
t(8,21)= ETO
t(15,17) = PML-RAR

7 (ara C) +3 (anthracycline)
ATRA for APML
ALL
tDt+
Tissue infiltration (LAD, splenomegaly, CNS, testes)

Good:
t(12,21) = TEL/AML
Hyperploidy

Bad:
t(9,22) = Philadelphia (BCR-ABL)

CNS px
CLL
CD5, 23, 19, 20 +
Smudge cells

Complications:
Hemolytic anemia
Ricther transformation to Large B-cell

Bad:
Zap 70
17q deletion
CD38+

Reye Staging: ↑ lymphocytes → accumulate LN → accumulate Spleen → accumulate BM (BM failure)
0 = lymphocytosis
1= LAD
2= splenomegaly
3= Anemia
4= thrombocytopenia

Tx: Wait and Watch
Hairy Cell
+TRAP
Hairy cytoplasmic process

Tx: 2-CDA (cladribine)
HL=
RS cells → B-symptoms
CD15, 30+, 20- (except: Lymphocyte predominant)
Localized LAD

Stage:
1
1 LN
2 = >1LN same side diaphragm
3 = >1LN diff side diaphragm
4 = extranodal

ABVD:
Adriamycin
Bleomycin
Vinblastine
Dacarbazine
Follicular Lymphoma=
t(14, 18)
Bcl2
CD19, 20, 10+
BM: Paratrabecular lymphoid aggregates

Rituximab + Bendamustine
Marginal Lymphoma
MALToma (H. pylori)
Lymphoepithelial lesions (destroy glands)

Antibiotic
Mycosis Fungoides
Sezary cells
Microabscesses (epidermis)
Diffuse Large B cell
CD19, 20

Bad:
APLES = age >60, performance status, LDH, extranodal, Stage 3, 4

R-CHOP:
Rituximab
Cyclophosphamide
HydroxyDaunrubocin
Oncovine
Prednisone
Brukitt’s=
t(8,14)
C myc
Starry Sky
CD10, 20, BCl6
African -- EBV

CNS prophylaxis
Mantle cell lymphoma
t(11,14) = Cyclin D
CD5, 20+, 23- (ddx CLL)
Lymphoblastic Lymphoma
similar to ALL:
+tDt
Mediastinal (thymus) enlargement

CNS prophylaxis
Clinical features & tx for all MPD?
panhyperplasia (↑ of all myeloid cells) -- Hydroxyurea
Jak 2 mt -- Ruxolitinib
Splenomegaly
For the following give me Clinical features, Ddx, Tx
---
Polycythemia Vera
↑ RBCs, ↓ EPO (-ve feedback)
Venous thrombosis (RBC viscosity)

Ddx:
Reactive Polycythemia = ↑ RBCs, ↑ EPO
- Lung dz = ↓ O2 sat
- Renal dz, Ectopic = nl O2 sat

Phlebotomy
Essential Thrombocythemia
↑ platelets (>600k) → Thrombosis

Ddx:
Reactive Thrombocytosis
-Fe deficiency anemia → ↑ serum ferritin

Antiplatelet therapy
Myelofibrosis
↑ stromal cells → ↑ PDGF → marrow fibrosis
Tear Drop cells

BM transplant
Chronic myelogenous leukemia (CML)
↑ granulocytes
Ph+ =t(9,22)
Basophillia

Progress to Acute Leukemia w/ out tx:
1. Chronic phase (Premalignant) = asymptomatic
2. accelerating phase
3. Blast phase (malignant) -- >20% blasts -- acute leukemia

Ddx:
Leukemoid rxn
- High LAP

Imatinib Mesylate (gleevac) = Tyr K (-)