Rx_2.25 (HemOnc) Flashcards
1
Q
Fatigue, anorexia, weight loss + enlarged lymph nodes + blood smear ==> dx?
A
- chronic lymphocytic leukemia (CLL) vs. small lymphocytic lymphoma (SLL)
- CLL = >4000cells/mm3 in bloodstream (more than SLL)
- “smudge cell” = characteristics finding on peripheral smear
- fragile lymphocytes (B cells) are flattened in theprocess of examining smear
- CD5
- CD19
- CD20
- CD23
- fragile lymphocytes (B cells) are flattened in theprocess of examining smear
2
Q
Warm-reactive autoimmune hemolytic anemia presentation and tx
A
- sx/labs
- jaundice
- anemia sx/lab findings
- increased retic count
- positive warm-agglutinin test
- tx
- corticosteroids ==> interfere w/immune destruction of erythrocytes
- inhibit Fc receptor-mediated clearance of sensitized RBCs
- corticosteroids ==> interfere w/immune destruction of erythrocytes
3
Q
Txs of autimmune hemolytic anemias
A
- IVIg ==> adult autoimmune hemolytic anemia
- cyclosporine ==> tx of refractory autoimmune hemolytic anemia in children
- splenectomy ==> tx in children w/chronic or refractory autoimmune hemolytic anemia
4
Q
Direct vs. Indirect Coombs test
A
- direct
- anti-IgM/IgG added to patients serum
- RBCs agglutinate if IgG/IgM is attached to the surface
- indirect
- normal RBCs added to patient’s serum
- if pt. has antiRBC antibodies ==> attach to normal RBCs
- add anti-IgM/IgG; RBCs agglutinate if anti-RBCs have attached
5
Q
Positive Coombs test indicates ==> ?
A
[most likely] autoimmune hemolytic anemia
6
Q
Tx of acute DVT/PE
A
- LMWH
- e.g. enoxaparin
- MOA: subq admin, inhibition of factor Xa
- does not require monitoring
7
Q
In warfarin tx, monitor…
A
- PT (prothrombin time) = measure of extrinsic coag pathway
- not standardized between labs
- INR = standardized between labs
8
Q
In heparin tx, monitor…
A
- PTT (partial thromboplastin time) = measure of intrinsic coagulation pathway
9
Q
Unfractionated Heparin: MOA
A
- activation of antithrombin III ==> decreased level of available thrombin
- inhibition of factor Xa
10
Q
Serious complications of heparin
A
- bleeding
- heparin-induced thrombocytopenia )HIT)
- antibodies against heparin-platelet factor 4 complexes ==> clotting
- ==> MI, stroke, DVT
- platelets ==> < 50% of prev. level
- occurs w/in 5-14 days
11
Q
Heparin antidote
A
protamine sulfate
12
Q
Characteristics of hemophilia
A
- x-linked recessive hematologic disorders
- A = factor VIII deficiency
- B = factor IX deficiency
13
Q
Translocations assoc. w/hematologic malignancies
A
- Burkitt’s lymphoma = t(8;14)
- 8 = c-myc
- 14 = IgG heavy chain locus
- ==> overexpression of c-myc
- CML = t(9;22)
- BCR-ABL fusion ==> increased tyrosine kinase activity
- Mantle Cell lymphoma = t(11;14)
- 11 = cyclin D1
- Follicular lymphoma = t(14;18)
- 18 = BCL2 ==> inhibits apoptosis
- AML (acute pro-myelocytic leukemia) = t(15;17)
- 17 = retinoic acid receptor
14
Q
fatigue, weight loss + enlarged spleen + peripheral smear ==> dx?
A
- hairy cell leukemia
- B-cells have “hairy” appearance
- rarely presents w/fevers and night sweats
- 4x more prevalent in men vs. women
- elevation of tartrate-resistant acid phosphatase @ B-lymphs in bone marrow = confirmation
- “TRAP the HAIRY beast”
15
Q
older pt w/central area of necrosis + ring enhancing lesion @ R hemisphere ==> dx?
A
- Glioblastoma multiforme
- “pseudopalisading necrosis” = central necrosis + hypercellular zone
- most common primary intracrainal neoplasm
- usually @ older patients
- poor prognosis