last min facts Flashcards
calculate ejection fraction
Ef=(EDV-ESV)/EDV
Ef= SV/EDV
Normal >55%
Immunohistochemistry test and 5 examples
using an antibody to detect a intermediate filament protein
Vimentin –> sarcomas
Desmin –> rhabdomyosarcoma
Cytokeratin –> epithelial tumors (squamous cell carcinoma)
GFAP –> astrocytoma, glioblastoma
Neurofilaments –> neuroblastoma
IL-5 (3 things) and who secretes it?
- promotes growth and differentiation of B cells.
- Enhances class switching to IgA
- Stimulates growth and differentiation of eosinophils
(secreted by Th2 cells)
where do ubiquitin tagged proteins get degraded?
proteasome
what type of cancer comes from calcitonin “C cells”
Medullary Carcinoma –> sheets of granular cells embedded in hyaline stroma
neural plate is present, but neural tube not yet complete…what day am I?
Roughly day 12
what day does neural tube close
day 28
MS lesions with vision think what?
MLF…always
E. Coli infection, pt in sepsis, what is virulence factor?
LPS endotoxin (lipopolysaccharide)
melanoma in-situ
lentigo maligna…consists of malignant cells but does NOT show malignant growth
seborrheic keratosis
waxy brown wart
noncancerous
originated is outer layer of keratinocytes
“stuck on”
Leser-Trélat sign
sudden appearance of multiple seborrheic keratoses, indicating an underlying malignancy (eg, GI, lymphoid)
left shoulder referred pain in context of internal bleeding
Kehr Sign: it is irritation of the diaphragm signaled by the phrenic nerve because the supraclavicular nerves have the same cervical nerve origin as the phrenic nerve –> this is commonly seen in a splenic rupture, ruptured ectopic pregnancy, or any other internal bleeding
ipsilateral CN III palsy mydriasis (“blown pupil”); may also see ptosis, “down and out” eye….caused by what?
Posterior communicating artery aneurysm rupture
down and out gaze
think occulomotor nerve…then need to decide if being compressed by PCA aneurysm, uncal herniation…
what does fick equation tell us?
CO=O2 consumption / (Art O2- Ven O2)
O2 consumption is proportional to body size/Hb
Art O2 is finger probe O2
Ven O2 is from Swan Ganz in pulm artery
SWAN GANZ GIVES US CO, and SVR
PCWP is equal to
LA pressure
all 3 types of shock share what characteristics?
low BP
high HR
Causes and hallmark of Cardiogenic shock
Causes: Acute MI, CHF, valvular dysfunction, arrhythmia
Hallmark: low CO caused by weak heart muscle..so all intracardiac pressure measurments are high (RA, RV, PCWP)
SVR is also high because body is clamping down trying to maintain BP
Hypovolemic shock, causes and hallmark
Causes: hemorrhage, dehydration, burns
Hallmark: low CO with ALL the internal heart measurments low (RA, RV, PCWP)
SVR is high to try to maintain BP
septic shock hallmark
hallmark –> LOW SVR
pressures are variable depending on early or late
take a bunch of acetaminophen, what do you do to liver?
deplete glutathione, replace with N-Acetylcysteine
organophosphate poisoning…FIRST STEP…then second step
GIVE ATROPINE FIRST!! (think that the organophosphate irreversibly inhibits the ACh-E, so have a shit ton of ACh. Need to give Atropine, a muscarinic antagonist to block these effects.
Then you can give Pralidoxime that regenerates ACh-E
acute intermitent porphyria enzyme
porphobilinogen deaminase
Remember 5 P’s
painful abd
port wine urine
polyneuropathy
psych
precipitated by drugs
what is the role of IkB in NF-kB signal transduction pathway
release NF-kB after undergoing phosphorylation
IkB INACTIVATES NF-kB
It is acted on by glucocorticoids
incidence calculation
new cases/# people at risk (during a specific time period)
platelet 804,000
leukocyte 146,000
anemia
this pt has CML
tx. imatinib
hydroxyurea mechanism and uses
mechanism: inhibits ribonucleotide reductase (disrupts purine and pyrimadine synthesis)
uses: sickle cell anemia (increase HbF), CML, Melanoma, polycythemia vera
foot drop
damage to deep peroneal nerve
what does dorsiflexion of the foot?
This is the deep peroneal nerve
- tibialis anterior
- extensor hallicus longus
- extensor digitorum longus
- peroneus tertius
treacher collins syndrome
neural crest dysfunction –> mandibular hypoplasia, facial abnormalities
This is a problem with the FIRST pharyngeal arch
micrognathia
glossoptosis
small lower jaw
downward displacement of the tongue
BOTH of these findings are seen in Pierre Robinson sequence…derivative of the 1st arch
phosphocreatine in the context of early exercise
phosphocreatine = creatine phosphate
can anaerobically donate a phosphate group to ADP to form ATP during the first 2-7 seconds following an intense muscular or neuronal effort
**This makes it so ATP does not fall appreciably in these first few seconds because remember that not much ATP is stored in a cell**
4yo boy with a karytotype of 47,XY+21 develops pancytopenia, lethargy, numerous bruises, pallor, and fever. Subsequent examination of bone marrow will show?
excess lymphoblasts
*need to remember that a kid with Down Syndrome has a higher risk of having ALL, which has MUCH increased Lymphoblasts
bladder anatomy
specifically, what is at the top of the trigone
These are the ureteric orifices
loss of peripheral vision in BOTH eyes to the LEFT. Metastatic tumor where?
Tumor in occipital lobe
SLE systemic sx
RASH OR PAIN
- *RASH OR PAIN:**
- *R**ash (malar A or discoid)
- *A**rthritis (nonerosive)
- *S**erositis
- *H**ematologic disorders (eg, thrombocytopenia) Oral/nasopharyngeal ulcers
- *R**enal disease
- *P**hotosensitivity
- *A**ntinuclear antibodies
- *I**mmunologic disorder (anti-dsDNA, anti-Sm, antiphospholipid)
- *N**eurologic disorders (eg, seizures, psychosis)
ruptured AAA, what see on physical exam
decreased femoral pulses
severe abd pain
tachycardia, low BP
pulsatile periumbilical mass
ampicillin/amox mechanism of resistance
penicillinase in bacteria (a type of B-lactamase)
NOT ALTERATION IN PCN BINDING PROTEIN…that is mechanism for cephalosporins
RANK and RANK-L
Osteoclast precursors express a cell-surface receptor known as RANK(RANK stands for Receptor Activator of Nuclear factor-Kappa B). Osteoblasts express RANKL (RANK Ligand) on the extracellular surface of their plasma membrane.
18mo boy with severe combined immunodeficiency syndrome requires a blood transfusion for severe anemia. Which blood product is most appropriate
irradiated RBC
*this kid has no immune system and nothing to fight any infection with. give him some clean shit
Hereditary hemorrhagic telangiectasia
=Osler-Weber-Rendu syndrome.
AD
Inherited disorder of blood vessels. Findings: branching skin lesions (telangiectasias), recurrent epistaxis, skin discolorations, arteriovenous malformations (AVMs), GI bleeding, hematuria
Displays incomplete penetrance
pouches vs arches
pouches –> endoderm. ears, tonsils, bottom, to, top
arches –> Mesoderm + neural crest. MOST of the stuff (cartilage, muscle, nerve)
remember CAP (ecto, meso + nc, endo)
ursodial
nontoxic bile acid
increases bile acid secretion, decrease cholesterol secretion and reabsorption
used for gallstone prevention in someone who does not want surgery
most dangerous type of Ehlers Danlos
Vascular type (deficient Collagen III- reticulin, blood vessels)
Berry Aneurysms
Hollow organ rupture
LIFE THREATENING…80% have vascular event by age 40
Menke’s vs Wilsons
Think of them as opposite
Menke’s: ATP7A gene, impaired copper absorption leads to decrease activity lysyl oxidase (requires copper as a cofactor so unable to cross-link collagen) –> brittle, kinky hair
Wilson’s: ATP7B gene, TOO MUCH COPPER
holoprosencephaly
trisomy 13
fetal alcohol syndrome
–> failure of midline cleavage of embryonic forebrain
drug that inhibits axonal transport along microtbules
colchicene
wallerian degeneration
anterograde degeneration
disappearance of axons and myelin sheats and secondary prolif of Schwann Cells
ependymal cells
produce CSF…they line the choroid plexus
neuromelanin
blackish intracytoplasmic pigment found in substantia nigra and locus ceruleus
(disappears w/ Parkinson)