3/6 UWORLD- test #34 Flashcards
Q 14. What cephalosporins (2) treat pseudomonas?
Third gen: Ceftazidime
Fourth gene: Cefepime
Q 14. What drugs treat pseudomonas? (6 drug classes)
- cephalosporins (ceftazidime, cefepime)
- aminoglycosides
- fluoroquinolone
- monobactem (aztreonam)
- carbapenems (-penem)
- broadspectrum penicilins (piperacilin, ticarcilin)
Q 1. suspensory ligament of ovary houses ovarian vessel. what is fancy word for this ligament? This ligament connects what?
infundibulopelvic ligament
connects ovary with lateral pelvic wall
Q 2. Which immune cells mediate killing of tumor cells ? Which cytokine mediates this?
NK cells
IL-2
Q 2. Which immune cells secrete IL-2? What cells does it stimulate for growth?
primarily from Helper T cells
Stimulates all sorts of T cells (helper, cytotoxic, regulatory) + NK cells
Q 3. What is glial fibrilary acidic protein? What cells show immunoactivity for this protein? What CNS tumors (2) will be positive?
- GFAP
- astrocytes
- glioblastoma multiforme & pilocytic astrocytoma
Q 3. What is synaptophysin? Which cells (3) will show immunoactivity for this protein?
- transmembrane glycoprotein in presynaptic vesicles
- neuron, neuroendocrine, neuroectoderm
Q 4. What determines severity of tetralogy of Fellot?
RVOT (right ventricle outflow tract) obstruction
-> will cause irreversible damage to pulmonary artery
- right ventricular hypertrophy could be reversible
Q 5. How AV shunt changes hemodynamics?
Arterioles bypass capillary and directly enters venous
-> thus it will increase venous return & preload
Q 6. When does beta thalessemia major become symptomatic? why?
After 6 month of child birth
Before 6 months, gamma globulin chain will be predominant form. So Fetal hemoglobin (HbF, two alpha, two gamma) will be normally functioning.
As Fetal hemoglobulin drops after 6 months, newborn baby cannot produce normal HbA, becoming symptomatic.
This rule applies to other beta globulin disorder (sickle cell disease)
Q 7. characteristics/functions of tRNA
- trinucleotide sequence in 3’end?
- D arm (dihydrourine)?
- T arm (ribothymidine, pseudouridine, cytidine)?
- 3’ end CCA
- D arm (dihyrdourine): tRNA recognition by correct aminoacyl-tRNA synthetase
- T arm (ribothymidine, pseudouridine, cytidine): tRNA ribosome binding
Q 7. Function of aminoacyl-tRNA synthetase? what part of tRNA ensure integrity of this enzyme’s reaction?
transfer of aminoacid to 3’OH end of tRNA
pairing of right aminoacyl-tRNA is mediated by D arm (dihydrourine)
Q 9. MRI finding of loss of grey-white matter with sulcal effacement suggests what?
hypoxic brain injury
possibly due to acute MI
Q 9. nuclei for eye: function? location?
- Edinger-westphal nucleus
- pretectal nucleus
- lateral geniculus nucleus
- Edinger-westphal nucleus: ipsilateral efferent CN3, located in upper midbrain
- pretectal nucleus: receives afferent CN2, sends BILATERALLY to Edinger-westphal nucleus, located in upper midbrain
- lateral geniculus nucleus: receives afferent CN2, sends ipsilaterally to calcarine sulcus for vision, located in thalamus
Q 9. Draw how CN2/CN3 are interconnected for pupillary light reflex
FA. 487
Q 10. Define psychologic term “avoidance”
vs. “schizoid”?
not socialize due to fear of criticism / rejection
Schizoid is voluntary withdrawal from socializing.
In avoidance, affect/repectfulness are intact, while schizoid is not.
Difference between antisocial vs. conduct disorder?
Disrespectful, violation of rights of others
- antisocial: > 18 yo
- conduct disorder: <18 yo
Q 10. Define 4 characteristics of boarderline disorder
- emotional instability
- suicidality & self-mutilation
(don’t confuse this with depression) - emptiness
- impulsivility