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75 Cards in this Set

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What are the three structural genes of HIV and what does each encode?
Pol: Enzymes
Gag: p24, p7
Env: gp160, gp120, gp41
What's going on here?
What's required for this to occur?
Arrow is pointing to a lymphoid follicle. Lymphoid follicle germ center is site of B-cell proliferation during immune response.

This is where B cells undergo isotype switching to other immunoglobulins, i.e., switch from IgM to IgG.

Requires CD40 receptor on B cell and CD40-ligand on activated T cells.
What is the main immunoglobulin of primary response?
Secondary response?
Primary response is IgM

Secondary is IgG
5 year-old
Fever, abdominal pain
Diarrhea with blood
Develops pallor, oliguria

Diagnosis
Pathophys
Lab values
Hemolytic uremic syndrome:
Microangiopathic hemolytic anemia + acute renal failure + thrombocytopenia

Usually assocd w/E coli O157:H7 and Shigella

Shiga toxin enters circulation from bowel and induces vascular damage leading to thrombus formation in capillaries

Widespread thrombi consume platelets and cause damage to RBCs

Resultant hemolytic anemia-->pallor, weakness, tachicardia

Thrombocytopenia-->purpura, petechiae

Labs will show:
Dec'd Hgb, HCT, RBC count
Inc'd LDH, retic
INC'D BLEEDING TIME due to reduced number of PLTs
Gram-positive bacteria that synthesize dextrans from sucrose

Identify
What does this allow?
Strep viridans

Dextrans facilitate adherence to fibrin

Fibrin and PLTs are deposited at sites of endothelial trauma, allowing bacterial adherence and colonization leading to formation of valvular vegetation

Note: Staph aureus is more aggressive and can adhere to intact endothelium without a preexisting lesion
S4 heart sound:
Describe when you'd hear it
Cause
End of diastole just before S1 (remember systole then diastole in terms of heart sounds)

Due to LVH

Heard at apex
55 year-old alcoholic
Treated with IV saline with dextrose
Develops anterograde amnesia, nystagmus, opthalmoplegia, ataxia

Diagnosis
Pathophys
Chronic EtOH-->low levels of thiamine at baseline
IV Dextrose without prior thiamine supplementation-->WERNICKE ENCEPHALOPATHY

Thiamine needed for pyruvate DH (involved in glucose metabolism)
Mammillary body undergoes necrosis bc brain can't properly metabolize glucose without thiamine (mammillary body is sensitive)

Mammillary body is part of Papez circuit (neural PW of limbic system involved in cortical control of emotion and memory)
List the B vitamins.
B1 - thiamine
B2 - ribioflavin
B3 - niacin
(B5 - pantothenic acid)
B6- pyridoxine
B7 - biotin
B9 - folic acid
B12 - cobalamin
Label
A - fornix (bundle of axons originating from hippocampus projecting to mammillary body)--can be affected in Wernicke encephalopathy

B - Mammillary body
C - Pons
D - Thalamus
E - Inferior colliculus (audition)
F- corpus callosum
Infant born with small phallus
Hypospadias
Testes in inguinal area
Normal Testosterone
Normal BP
46XY

Diagnosis
Pathophys
5-alpha-reductase deficiency

T allowed for dev't of internal genitalia
DHT (which was lacking) is required for dev't of external genitalia. Lack of DHT-->feminization

This will resolve during puberty
List the enzyme deficits found in congenital adrenal hyperplasia, and their effects (lab wise and presentation wise).
21-hydroxylase: dec'd corticosteroids and mineralocorticoids, inc'd testosterone; ambiguous genitalia in females, salt wasting

11-hydroxylase: dec'd cortisol, corticosterone, aldosterones; inc'd testosterone
Ambiguous genitalia in females; fluit/salt retention, hypertension

17-hydroxylase: inc'd mineralocorticoids, dec'd sex hormones, corticosteroids.
All pts phenotypically female
Fluit and salt retention, HTN
0x50 + 1x30 + 2x10 + 3x10 = 80

80/100=0.8
7 year-old male
Colicky abdominal pain
Arthralgia
Proteinuria
Palpable lesions on lower extremities

Diagnosis
Pathophys
Henoch-Schonlein purpura
Deposition of IgA immune complexes on BV walls and within renal mesangium activates complement-->inflammation

Elevated serum IgA and circulating IgA-containing immune complexes
How does diphtheria cause disease?
Must acquire virulence via bacteriophage-mediated "infection" with Tox gene which codes for diphtheria AB exotoxin

Bacteriophage = Corynephage beta
Process = lysogenization
How does V, Q, V/Q differ by region of the lung (while standing)?
Base:
Q is much higher (gravity!)
V is higher
V/Q is lower

Apex:
Q is very low
V is low
V/Q is high
What's an arteriovenous shunt?

How does this affect LV pressure-volume loops?
AV fistula = abonrmal communication between artery and vein that bypasses capillary beds (major source of resistance to vascular system)

Thus AV shunts allow blood under arterial pressure to directly enter venous systems

Manifests as a thrill on palpation (and bruit on auscultation)

AV shunts increase cardiac preload by increasing rate and volume of blood flow back to heart (will increase to right horizontally; no increase in pressure).
What is the effect of alpha-1-antitrypsin deficiency on lung compliance?
Results in panacinar emphysema (and liver cirrhosis)-->compliance of lung parenchyma increases
Patent Ductus Arteriosus:
Specific embryonic origin
Conditions associated with it
6th aortic arch

PDA Associated with prematurity and congenital rubella
Hypertrophic CM:
Genetic cause
Mutation to cardiac sarcomere proteins; most involving-beta-myosin heavy chain
Dilated CM:
Genetic cause
Mutations of cardiac myocyte CYTOSKELETAL proteins (DYSTROPHIN) or mitochondrial enzymes
Orotic aciduria:
Pathophys
Presentation
Treatment
Disorder of pyrimidine metabolism

Defective enzyme is orotate phosphoribosyl transferase and OMP decarboxylase--these catalyze conversion of orotate to uridine monophosphate.


Presents with Hypochromic megaloblastic anemia
Excretion of orotic acid in urine
Anemia, neurlogic abnlts
Growth retardation

Treat with uridine supplementation (will inhibit carbamoyl phosphate synthase II--first enzyme of pyrimidine synthesis)
20 year-old male
African American
Malaiase, dark urine
Mild UTI several days ago
Anemic with Heinz bodies

Diagnosis
G6PD deficiency

Likely given TMP-SMX (OXIDATIVE STRESSOR) for UTI
Glucose-6-phosphate DH:
Function (general and specific)
Glucose-6-phosphate + NADP+ --> 6-phosphogluconate + NADPH

Need to produce NADPH (part of HMP shunt) to maintain glutathione in REDUCED state (important for protection of RBCs x oxidative damage)
X-ray shows fractured 12th rib on left side.

What structure is likely to be lacerated by broken rib?
LEFT KIDNEY

Spleen is near left 9th, 10th, 11th kidney.
What drugs are likely to cause seizures?
Bupropion (antidepressant)
INH (anti-tb if given without pyridoxine)
Imipenem (abx)
TCA:
Side effects
Cadiac arrhythmias (QRS, QT elongations much like quinidine)
Sedation (antihistamine f/x)
Urinary retention (antich f/x)
COX--1 vs COX-2:
Roles
COX-1: physiologic role in NORMALLY functioning tissue, e.g., PLATELETS, the GI TRACT

COX-2: Expressed at sites of inflammation
Celecoxib:
MOA
Selective COX-2 inhibitor

Doesn't inhibit COX-1 (which is involved in NORMAL function--PLATELETS and GI TRACT)
Nitroglycerin:
Specific molecular MOA
Drug is converted into NO at vascular smooth muscle cell membrane

Within the smooth muscle cell, NO stimulates gunaylate cyclase to convert GTP into cyclicGMP

Increasing [ ] of cGMP within cell-->dec'd intracellular Ca2+
-->Dec'd activity of myosin light-chain kinsae
->Myosin light chain DEPHOSPHORYLATION and smooth muscle relaxatio n
Draw the intrinsic and extrinsic pathways.

Which is affected by which hemophilia?
Treatment?
Hemophilia A: VIII deficiency
Hemophilia B: IX deficiency

These are both part of intrinsic PW. Need both factors to activate Factor X.

If needed to treat, could administer thrombin.
6-year old male
Prolonged bleeding after dental extraction
h/o hemartrhosis after minor trauma

Diagnosis
Mode of inheritance
Hemophilia
X-linked RECESSIVE
14 year-old boy with hemophilia
Parents have no bleeding problems
Older sister without this condition is pregnant (sex of child unknown)

What is the risk her child will be affected?
Hemophilia is X-linked RECESSIVE

Chance sister is a carrier is 1/2

Chance child will be affected is 1/8
38 year-old male
IVDU
High-grade fever, fatigue, dyspnea

Diagnosis
Staph aureus tricuspid valve endocarditis-->septic emboli to lungs (hemorrhagic)
Pathology
Wedge-shaped hemorrhagic pulmonary infarcts

Hemorrhagic due to dual blood supply to lungs (pulmonary and bronchial arteries)

If pt is IVDU-->right heart endocarditis (S aureus)-->septic embolization
Contraindications of OCPs
h/o thromboembolic event/stroke
h/o estrogen-dependent tumor
Women >35 who smoke
Hyper-TG
Liver dz
Pregnancy
Non-immune effects of glucocorticoids
Muscle weakness, skin thinning, impaired wound-healing, osteoporosis

INCREASED LIVER PROTEIN SYNTHESIS, specifically enzymes involved in gluconeogenesis and glycogenesis; contributes to hyperglycemia
24 year-old male in coma
Cyanotic, unresponsive to painful stimuli
BP 100/60, pulse 100
RR 5/min, Temp 98F
Pupils constricted, poorly responsive to light

Diagnosis
Treatment
Treatment MOA
Opioid overdose

Treat with Naloxone (an opioid receptor antagonist)--works by blocking Mu receptors of opioid receptors (this is where narcotics bind FYI)
Signet ring cell-->Gastric adenocarcinoma
65 year-old male
Abdominal pain in waves
Nausea, vomiting
Ileocecal obstruction

Diagnosis
What would you see on radiograph?
Gallstone ileus--large gallstone intermittently obstructing lumen causing waxing/waning syx

Eventually gallstone may come to rest in ileum (smallest lumen of GI tract)

Abdominal radiograph would show air in biliary tree
63 year-old male with PE

Where could filter be placed to prevent further embolization?
IVC filter--designed to prevent travel of DVT from legs to lung vasculature
Label
A) Duodenum
B) IVC (note R Renal Vein drains into it)
C) Abdominal Aorta
D) Ileum (figure 8)
E) L Renal Vein
Diagnosis
Pathophys
(MPA = main pulmonary artery)

This is a saddle embolus likely due to DVT (endothelial damage, venous stasis, hypercoagulable state)
The IVC is located to the _______ of the vertebral bodies.
Right
Which veins join to form the IVC?
Common iliac vv
Phenytoin:
MOA
Use
Side Effects
MOA: INhibits neuronal high-frequency firing by reducing ability of Na+ channels to recover from inactivation (increasing refractory period)

Use in epilepsy

Generalized LAD
Hirsutism
Gingival hypertrophy
Valproic acid:
AE
Severe hepatotoxicity, measure LFTs
Carbamazepine:
AE
Agranulocytosis
How does a thrombus originating from atherosclerosis differ from a thrombus originating from venous stasis?
Atherosclerotic thrombi affect the arterial tree (likely to cause stroke--something arterial in route)

Venous stasis is going to affect the venous tree (pulmonary artery)--not due to atherosclerosis!
Biochemical effects of folate deficiency.

Draw normal pathway.
Provide lab values/effects.

What other B vitamin is necessary?
Will lead to inc'd homocysteine levels, inability to reproduce methionine.

And megaloblastic anemia.

Need B6 (pyridoxal phosphate)!
Need folate to make TH4!
24 year-old male
Sickle cell disease
MCV 114
Reticulocytes 5%

Diagnosis
Pathophys
Megaloblastic anemia due to folate and B12 deficiency

Due to inc'd RBC turnover

Low folic acid levels impair DNA synthesis, while leaving RNA synthesis unaffected. Cytoplasmic components then accumulate within slowly dividing RBCs-->produces larger RBCs.
Define facilitation.
WHen interviewer encourages patient to talk more about his/her experience

"And then what happened?"
Define reflection.
When physician repeats what patient tells him

"So, you're telling me you were molested as a child."
Define confrontation.
Therapist draws patient's attn to discrepancies in responses

"Although you're telling me you were disturbed by this trauma, you sound unaffected as you're describing it"
Amphotericin B:
AEs
Renal vasoconstriction-->dec'd GFR

May even be directly toxic to renal empithelium-->acute tubular necrosis, electrolyte disturbances
32 year-old man
Sharp mid-chest pain that worsens with deep inspirations
Pain decreases when he sits up
Respiratory illness one week ago
Diagnosis
Auscultative findings
Pathophys
Sharp and pleuritic chest pain (increases with breathing, decreases with sitting up and leaning forward)-->acute pericarditis

Would hear FRICTION RUB (high pitched, leathery, scratchy)

Can be caused by MI, rheumatic fever, uremia, but likely due to infectious cause given h/o respiratory infection
32 year-old female
Infertile
Menstruates 2-3 times per year
Hirsutism
Obese

Diagnosis
Hormone Imbalances
Risks
Obesity + hirsutism + oligomenorrhea ---> PCOS

Due to abnl HPA-Ovarian system

Androgen and LH levels elevated, FSH normal. Inc'd LH/FSH (>3) characteristic

Menstrual irregularity due to anovulation

Risk of endometrial adenocarcinoma (high levels of unopposed estrogen)

Inc'd insulin resistance-->obesity (higher risk of DM II)

Hirsutism/acne-->inc'd androgen levels

Changes of lipid metabolism-->inc' drisk atherosclerosis and CAD
8 year-old male
Throat pain, fever, malaiase
Returns in month with fatigue, joint pain
Later develops heart murmur

Diagnosis
Pathophys
Acute rheumatic fever

It follows untreated Group A Strep pharyngitis. Syx result from structural homology between antigenic determinants (epitopes) on GAS and on human cardiac, CNS, and cutaneous tissue (Resulting in a rash!)
Mullerian ducts AKA
Paramesonephric (upper vagina, uterus, uterine tubes, cervix)
Wolffian ducts AKA
Mesonephric
How do T and DHT differ in roles of male development?
T = internal genitalia
DHT = external genitalia
Role of Omalizumab in asthma
Anti-IgE antibodies: binds to IgE to inhibit its action on mast cells, basophils--this decreases the allergic response.

Minimizes allergic responses of asthma. Are able to discontinue glucocorticoids and decrease use of steroids.
Molecular effects of diphtheria exotoxin.

Treatment?
AB exotocin ribosylates and deactivates elongation factor 2, thus inhibiting human protein synthesis--results in sore throat, fever, LAD, dyspnea, odynophagia.

Tx:
1. diphtheria antitoxin (inactivates all circulating toxin, but not those that have gained access to cardiac or neural cells; known as passive immunization)
2. PCN/erythromycin (kills bacteria in cells)
3. DPT vaccine (prevents future infection)
Where are lipids digested and absorbed?
Lipids (TGs, cholesterol, phospholipids) digested in duodenum and absorbed in jejunum.
What is the effect of cholecystectomy on lipid digestion and absorption?
Little effect--liver continues to produce bile acids, just doesn't have a place to store it. Expect inc'd blood flow to liver for this reason.

Only difference for patient will be difficulty consuming large fatty meals.
injury to Gunyon's canal
Ulnar nerve
List regions of the arm that may injure underlying nerves (also provide nerves).
Surgical neck of humerus: axillary

Head of radius: deep branch of radial nerve

Medial epicondyle of ulnar: ulnar

Carpal tunnel: Median nerve

Hook of hamate, Gunyon's canal: Ulnar
Newborn develops vomiting, lethargy
Mother states diapers smell like burned sugar

Diagnosis
Pathophys (include biochemical pathway)
Treatment
Maple Syrup Urine Disease--due to defective breakdown of branched chain amino acids: LEUCINE, ISOLEUCINE, VALINE

Specific defect in alpha-keto acid DH, resulting in elevated serum/tissue levels of alpha-keto acids (NEUROTOXICITY)

Urine has sweet odor.

Enzymes needed to metabolize L, I, V requires: Thiamine, FAD, NAD, Lipoate, CoA (Tx = dietary restriction and thiamine)
Elastin fibers in the alveolar walls of the lungs can be stretched easily during inspiration and recoil to their original shape once the force is released.

How?
Elastin has lysine groups which are crosslinked between 4 other lysine residues on 4 different elastin chains.

This crosslinking is accomplished by extracellular lysyl hydroxylase.

Note: elastin ≠ collagen!
What is the role of CFTR in sweating? How does it differ in cystic fibrosis?
When sweating, fluid is initially isotonic with ECF.

CFTR then reabsorbs Cl- and Na+ to make hypotonic sweat.

In CF, there is less reabsorption of Na+ and Cl-.
Infant
Bilateral cleft lip
Microcephaly
Microphthalmos
Omphalocele
Trisomy 13: Patau

Could also see:
Neural Tube defects
PDA
PCKD
Pyloric Stenosis
ROCKER-BOTTOM FEET
POLYDACTYLY
Bacterial transpeptidase:
Role
What antibiotics target it?
Transpeptidases are a form of PBP that cross-link peptidoglycan in bacterial cell wall

Inhibited by PCN and cephalosporins
Which antibiotic targets nuclear proteins?
Fluoroquinolones target nuclear proteins (DNA GYRASE)
Which antibiotic targets the formation of cell wall glycoproteins?
Vancomycin
Which antibiotic targets ribosomal proteins?
Macrolides
Tetracyclines
An isolate of streptococcus pneuomoniae is incubated with low-dose radiolabeled ceftriaxone and subjected to protein electrophoresis.

Five bands are detected by radioautography.

Another isolate from a different patient undergoes the same protocol but electrophoresis only yields two bands.

What accounts for the difference?
Change in protein structure (PCN BP); must indicate that for second patient, three of the the PCN BPs have been altered in such a way that inhibits binding of ceftriaxone.