Shit - Heme UWorld Flashcards
Erb-B2
Her-2-nu
Ab = trastuzumab
Fibrin selective thrombolytic:
vs.
non-selective:
Selective = tPA, alteplase, reteplase, tenecteplase
Non-selective = streptoknase, urokinase
Which cancer creates a tyrosine kinase fusion protein
CML: bcr-abl
Rx = imatinib (binds TK)
enoxaparin, dalteparin, fondaparinux
LMWH
binds AT-III promoting Xa inactivation
Prothrombin
Factor II
PNH triad
Pancytopenia: acquired stem cell mutatoin, so other lineages mutated too; can also be aplastic anemia
Negative coombs HA: loss of GPI anchor, so no CD55 or CD59 to inhibit MAC
Vanous thromboses (i.e. budd-chiari): prothrombotic factors released from lysed RBCs and platelets
Reed-sternberg =
HODGKINS
yellow-brown pigment =
lipofuscin OR hemociderin
Cytic AND solid brain tumour in kids
Pilocytic astrocytoma
Lung cancer with neuroendocrine markers
(synaptophysin, chromogranning, neurofilaments, neuron-specific enolase
Prolonged PTT but normal PT and thrombin time = deficiency in:
VIII, IX, XI, or XII
von Willibran disease inheritance
AD with variable penetrance
increased bleeding time indicates:
platelet problem
Cox -1 vs Cox- 2 funcitons/AE
Cox-1 blocks TXA-2, so prevents clots/causes bleeding; also blocks PG-I
Cox-2 blocks PGs (and PG-I only wrt blood sutff), so anti-inflammatory but pro-coagular/anti-bleeding
CCl4 causes
free-radical damage
Dysplasia vs carcinoma?
reversibility
MC location of cancer in LiFraumeni
breast, brain, adrenal cortex, sarcomas, leukemias
Angiogenesis GFs
VEGF (can be stimulated by IL-1 and IFN-g)
FGF
Aplastic anemia classic signs
BM: hypocellular with fatty replacement and stroma
Spleen: NO splenomegaly to complensate (because stem cell problem)
Non-truma foot/wrist drop
Churg strauss
Lead poisoning
Shortest t1/2 of CFs and result
VII
In liver problems, PT is first thing to be elevated
(most CFs made in liver)
vincrinstine AE
neurotoxicity: tingling in fingers and toes (peripheral neuropathy)
leucovirin
aka folinic acid
THF derivative that doesnt need DHF-reductase to be activated
Rescure for BM suppression, mucositis, GI problems
infliximab
Anti-TNF-a
rituximab
MAb-CD20
cancer with altered PDGF
chronic myelomonocytic leukemia
Protein C resistance
Factor V leiden mutation
Functions of the genes in cancer translocations:
- 8;14
- 14;18
- 11;14
- 9;22
- 15;17
- 8;14: 8 = c-myc = TC activator = burkitts
- 14;18: 18 = bcl-2 = blocks apoptosis = follicular
- 11;14: 11 = cyclin D1 = cell cycle regulator = mantle cell
- 9;22: 22 = abl = tyrosine kinase (cyto + nuc) = CML
- 15;17: 15 = RAR = myelocyte differentiation = PAML
glucose and heme synthesis
glucose inhibits ALA-synthase
Rx for AIP
(also blocked by heme)
painless waxing and waning LAD
follicular lymphoma
cachexia hormone
TNF-a (cachexin)
microsomal monooxygenase
= CYP450
Overexpression converts more pro-carcinogens to carcinogens, increasing risk of cancer
kid with blasts in periphery with trouble breathing and swallowing
T-ALL via mediastinal thymic mass
Raltegravir
Prevents integration, thus host from making virus mRNA
hematology drug causeing neutropenia presenting as fever and mouth ulcers
Ticlopidine (ADP-R blocker)
use only if allergic to asprin + clopidogrel
PE:
acute management
vs
longterm prevention DOC
Acute = herparin
longterm = warfarin
lymphocytosis + low ALP
CML
P glycoprotein mechanism
ATP-dependent transporter
in bacteria and cancer cells
PUre recc cell aplasia: causes
IgG of CD8 against erythroid precursors/progenitors.
Often linked to thymomas and lymphocytic leukemias
why do pregnancy catastrophies cause DIC?
Thromboplastin (TF/CF III) released from placenta
Hemolysis in G6PD
INH, sulfonamides, dapsone, asprin, ibuprofen, primaquine, nitrofurantoin
most important prognostic factor
STAGE = TMN (alnd invasion)
(NOT grade = level of differentiation)
Myeloperoxidase +ve leukemia
AML
(also see auer rods, these are what stain)
Isolated increase in BT
Bernard soulier (no GpIb)
ASA (decrease TXA2)
Uremia (platelets to aggregate/adhere properly)
cisplatin/carboplatin nephrotoxicity rescue
Amifostine and chloride saline diuresis