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30 Cards in this Set

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270. Burkitt’s Chromosomal translocation and gene affected?
a. t(8;14) c-myc activation.
271. Follicular lymphoma Chromosomal translocation and gene affected?
a. t(14;18) bcl-2 activation.
272. M3 AML Chromosomal translocation?
a. t(15;17) -responsive to all-trans retinoic acid.
273. Ewing’s sarcoma Chromosomal translocation?
a. t(11;22)
274. Mantle cell lymphoma Chromosomal translocation?
a. t(11;14)
275. Langerhans cell histiocytosis (LCH) and what do defective cells express?
a. Proliferative disorders of dendritic (Langerhans) cells.
b. Defective cells express S-100 and CD1a.


Jeef note: If its S-100 it must be neural crest in origin
276. Characteristic histo feature of Langerhans cell histiocytosis?!?!
a. Birbeck granules “tennis rackets” on EM.
277. 4 chronic myeloproliferative disorders?
1. Polycythemia vera
2. Essential thrombocytosis
3. Myelofibrosis
4. CML
b. The myeloproliferative disorders represent an often-overlapping spectrum, but the classic findings are described below.
278. RBCs, WBCs, Platelets, JAK2 mutations in Polycythemia vera?
a. RBCs: ↑
b. WBCs: ↑
c. Platelets: ↑
d. JAK2 mutation: Positive.
279. Polycythemia Vera classic findings?
a. Abnormal clone of hematopoietic stem cells are increasingly sensitive to growth factors.
280. RBCs, WBCs, Platelets, JAK2 mutations in Essential thrombocytosis?
a. RBCs: -
b. WBCs: -
c. Platelets: ↑
d. JAK2 mutation: Positive (30-50%)
281. Essential thrombocytosis classic findings?
a. Similar to polycythemia vera, but specific for megakaryocytes.
282. RBCs, WBCs, Platelets, JAK2 mutations in myelofibrosis?
a. RBCs: ↓
b. WBCs: variable
c. Platelets: variable
d. JAK2 mutation: Positive (30-50%)
283. Myelofibrosis classic findings?
a. Fibrotic obliteration of bone marrow.
b. Teardrop cell
c. “Bone marrow is crying because its fibrosed”
284. RBCs, WBCs, Platelets, JAK2 mutations in CML
a. RBCs: ↓
b. WBCs: ↑
c. Platelets: ↑
d. JAK2 mutation: NEGATIVE
e. Philadelphia chromosome positive.
285. Significance of JAK2 in the myeloproliferative disorders?
a. JAK2 is involved in hematopoietic growth factor signalling.
b. Mutations are implicated in myeloproliferative disorders other than CML.
286. Plasma volume, RBC mass, O2 saturation, and EPO in Relative Polycythemia?
a. Plasma volume: ↓ (its basically just due to dehydration)
b. RBC mass: -
c. O2 sat: -
d. EPO: -
287. Associated causes of appropriate absolute polycythemia?
a. Lung disease
b. Congenital heart disease
c. High altitude
288. Plasma volume, RBC mass, O2 saturation, and EPO in Appropriate absolute polycythemia?
a. Plasma volume: -
b. RBC mass: ↑
c. O2 sat: ↓
d. EPO: ↑
289. Cause of Inappropriate absolute polycythemia?
a. Due to ectopic erythropoietin:
1. RCC (Renal cell carcinoma)
2. Wilm’s tumour
3. Cyst
4. HCC (Hepatocellular carcinoma)
5. Hydronephrosis
290. Plasma volume, RBC mass, O2 saturation, and EPO in Inappropriate absolute polycythemia?
a. Plasma volume: -
b. RBC mass: ↑
c. O2 sat: -
d. EPO: ↑
291. Plasma volume, RBC mass, O2 saturation, and EPO in polycythemia vera?
a. Plasma volume: ↑
b. RBC mass: ↑↑
c. O2 sat: -
d. EPO: ↓
292. MOA of Heparin?
a. Cofactor for the activation of antithrombin.
b. ↓ thrombin and Xa.
c. Short half-life.
d. Activates antithrombin, which ↓ the action of IIa (thrombin) and Xa.
293. Clinical use of heparin?
a. Immediate anticoagulation for pulmonary embolism, stroke, acute coronary syndrome, MI, DVT.
294. Can heparin be used during pregnancy?
a. Yes, does not cross placenta.
295. What coag value do you follow w/heparin?
a. PTT
296. AE of Heparin?
a. Bleeding
b. Thrombocytopenia (heparin-induced thrombocytopenia HIT)
c. Osteoporosis
d. Drug-drug interactions
297. Antidote for heparin?
a. Protamine sulfate.
b. Positively charged molecule that binds negatively charged heparin.
298. Difference with newer low-molecular-weight heparins such as enoxaparin?
a. Enoxaparin acts more on Xa, has better overall bioavailability, and 2-4 times longer half-life.
b. Can be administered subq and w/out laboratory monitoring.
c. Not easily reversible.
299. Heparin-induced thrombocytopenia (HIT)?
a. Heparin binds to platelet factor IV, causing antibody production that binds to and activates platelets leading to their clearance and resulting in a thrombocytopenic, hypercoagulable state!