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514 Cards in this Set

  • Front
  • Back
What is necrosis?
Non-Programmed cell death

Nucleus destroyed first
What is apoptosis?
Programmed cell death

No inflammation
What is pyknosis?
Nucleus turns into blobs
What is karryohexis?
Nucleus fragments
What is Karyolysis?
Nucleus dissolves
What is a somatotrope?
GH
What is a gonadotrope?
LH, FSH
What is a thyrotrope?
TSH
What is a corticotrope?
ACTH
What is a lactotrope?
PRL
What receptors do protein hormones use?
Cell membrane receptors
What receptors do steroid hormones use?
Nuclear membrane receptors
What are the steroid hormones?
"PET CAD"
Progesterone
Estrogen
Testosterone
Cortisol
Aldosterone
Vitamin D
*TSH (Acts like a steroid)
What does endocrine mean?
Secreted into blood
What does exocrine mean?
Secreted into non blood
What is autocrine?
Works on itself
What is paracrine?
Works on its neighbor
What is merocrine?
Cell is maintained (exocytosis)
What is apocrine?
Apex of cell is secreted
What is holocrine?
Whole cell is secreted
What organs do not require insulin?
BRICKLE
Brain
RBC
Instestine
Cornea/Cardia
Kidney
Liver
Exercising Muscle
What does GnRH do?
Stimulates LH, FSH
What doe GRH do?
Stimulates GH
What does CRH do?
Stimulates ACTH
What does TRH do?
Stimulates TSH
What does PRH do?
Stimulates PRL
What does DA do?
Inhibits PRL
What does Somatostatin do?
Inhibits GH
What does ADH do?
Conserves water, vasoconstricts
What does oxytocin do?
Milk letodwn
baby letdown
What does GH do?
IGF-1 Release from liver
What does TSH do?
T3, T4 release from thyroid
What does LH do?
Testosterone release from testes. Estrogen and Progesterone release from ovary
What does FSH do?
Sperm or egg growth
What does PRL do?
Milk production
What does ACTH do?
Cortisol release from adrenal gland
What does MSH do?
Skin pigmentation
What are the stress hormones and time frames?
Epi: Immediate
Glucagon: 20 minutes
Insulin: 30 minutes
ADH: 30 Minutes
Cortisol: 2-4 hrs
GH: 24 hours
What does ADH do?
Concentrates Urine
What is Diabetes Insipidus?
Too little ADH (urinate a lot)
What is central DI?
Brain not making ADH
What is nephrogenic DI?
Block of ADH V2 Aquaporin receptor

Can be caused by lithium, demeclocycline
What is central DI?
Brain not making ADH
What does the water deprivation test tell you?
Water deprivation --> DI fails to concentrate urine
What does giving DDAVP tell you?
DDAVP central DI concentrates urine
What is SIADH?
Too much ADH---> expanded plasma volume
What is the difference between DI and SIADH?
DI has dilute urine
SIADH has concentrated urine
What is psychogenic polydypsia?
Pathologic water drinking ---> low plasma osmolarity
What does aldosterone do?
Reabsorbs Na and 3 waters
Secretes H+ via H/K pump
What is a neuroblastoma?
Adrenal tumor in kids
Dancing eyes/feet
Secretes catecholamines
What is a pheochromocytoma?
Adrenal medulla tumor in adults
What does Z. Glomerulosa make?
Aldosterone "salt"
What does zona fasciculata make?
Cortisol "sugar"
What does Zona reticularis make?
androgens "sex"
What is Conn's syndrome?
High Aldosterone (tumor--primary)
What does ANP do?
Inhibits aldosterone
Dilates renal artery (affterent arteroiole)
What does calcitonin do?
Inhibits osteoclasts --->low serum Ca2+
What is MEN 1
Wermer's 3 P's
Pancrease
Pituitary
Parathyroid
What is MEN II a
Sipple's
Pheochromocytoma
Medullary carcinoma of the Thyroid
+/- Parathyroid
What is MEN II b
Pheochromocytoma
Medullary carcinoma of the thyroid
Oral/GI Neuromas
What does CCK do?
Gallbladder contraction
What does cortisol do?
Gluconeogenesis by proteolysis --->thin skin
What is Addison's disease?
Autoimmune destruction of adrenal cortex
What is Waterhouse Friderichsen?
Adrenal hemorrhage
What is Cushing's syndrome?
High Cortisol
Pituitary tumor, adrenal tumor or small cell CA of the lung
What is Nelson's syndrome?
Hyperpigmentation after adrenalectomy
If low dose dexamethasone test supresses, what does taht tell you?
Depressed, obese or normal variant
If low dose Dexamethasone test does not supress, what does that tell you?
Cushings. Do high dose test
If high dose Dexamethasone test supresses, what does that tell you?
pituitary tumor -->ACTH
If high dose Dexamethasone test does not supress, what does that tell you?
Test ACTH

Low ACTH: Adrenal Adenoma -->cortisol

High ACTH: Small cell CA of the lung --->ACTH
What are the survival hormones?
Cortisol: Permissive under stress
TSH: Permissive under normal
What does epinephrine do?
Gluconeogenesis/
Glycogenolysis
What does Erythropoietin do?
Makesw RBCs
What does gastrin do?
Stimulates parietal cells to produce IF and H+
What does GH do?
Growth: sends somatomedian to growth plates

Gluconeogenesis by proteolysis
What is achondroplasia (laron dwarf)?
Abnormal FGF receptors in extremities
What is a midget?
Decreased somatomedian receptor sensitivity
What is acromegaly?
Adult bones stretch

Coarse facial features
Large, furrowed tongue
Deep, husky voice
Jaw protrusion
Increased IGF-1 d/t GH tumor
What is gigantism?
Childhood acromegaly
What does GIP do?
Increase insulin action leading to post prandial hypoglycemia
What does glucagon do?
Gluconeogenesis
Glycogenolysis
Lipolysis
Ketogenesis
What does insulin do?
Pushes glucose into cells and K+ follows
What is Type I DM?
Anti-islet cell Ab
Coxsackie B
Low insulin
DKA
Polyuria
Polydypsia
What is Type II DM?
Insulin receptor insensitivity
High Insulin
HONK coma
Acanthosis nigricans
How does DKA present?
Kussmaul respirations
Fruity breath (acetone)
Altered mental status
What is the Dawn phenomenon?
AM Hyperclycemia secondary to growth hormone
What is the Somogyi Effect?
AM hyperglycemia secondary to every gypoglycemia?
What is factitious hypglycemia?
Injected insulin (Increased insulin, decreased C Peptide)
What is an insulinoma?
Insulin secreting tumor (increased insulin and increased C peptide)
What is metabolic syndrome X?
"Pre DM"

HTN
Dyslipidemia
Hyperinsulinemia
Acanthosis Nigricans
What are foot ulcer risk factors?
DM/Glycemic Control
Male
Smoking
Bony abnormalities
Previous ulcers
What conditions cause weight gain?
Obesity
Hypothyroidism
Depressions
Cushing's
Anasarca
What does motilin do?
Stimulates Segmentation (primary peristalsis, MMC)
What does PTH do?
Stimulates osteoblast to turn on osteoclast
What does vitamin D do?
Helps in Ca2+ reabsorption from the GI tract
What do parathyroid chief cells secrete?
PTH
What do stomach chief cells secrete?
Pepsin
What is the difference between norepinephrine and epinephrine?
NE= neurotransmitter
Epi=Hormone
What is primary hyperparathyroidism?
Parathyroid adenoma
What is secondary hyperparathyroidism?
Renal failure
What is familial hypocalciuria/hypercalcemia?
Decreased Ca2+ excretion
What if both serum Ca and PO4 decrease?
Vitamin D Deficiency
What if serum Ca and PO4 change in opposite directions?
Hypoparathyroidism
What is the MCC of primary hypoparathyroidism?
Thyroidectomy
What is pseudohypoparathyroidism?
Bad kidney PTH receptor
Decreased urinary cAMP
What is pseudopseudohypoparathyroidism?
G Protein defect, no calcium problem
What is Hungry Bone Syndrome?
Remove PTH -->Bone sucks in Ca
What does secretin do?
Secretion of bicarb
Inhibit gastrin
Tighten pyloric sphincter
What does somatostatin do?
Inhibits secretin, motilin, CCK
What do T3 and T4 do?
Growth, differentiation
What disease has exopthalmous?
Grave's
What disease has enopthalmous?
Horner's
Grave's Disease
Expothalmos
Pretibial Myxedema
TSH receptor Antibody
Dequervain Disease
Viral (self limiting) hyperthyroidsm
Silent thyroiditis
Post partum hypothyroidism
Plummer's
Bening adenomona 50 yo hyperthyroidism
Jod-Basedow
Transient hyperthyroidism due to increased iodine
Hashimoto's Thyroiditis
Antimicrosomal Ab = TPO Ab
Reidel's struma
Woody

Hypothyroidism
Cretinism
Hypothyroid mom and baby
Euthyroid sick syndrome
Low T3 syndrome
Wolff-Chaikoff
Transient Hypothyroidism
What is Plummer's syndrome?
Hyperthyroid adenoma
What is Plummer-Vinson syndrome?
Esophageal webs
What does testosterone do?
Makes external male genetilia
What does Mullerian inhibiting factor do?
Makes internal male genetilia
What do TPO and Thymosin do?
Help T cells mature
What does VIP do?
Inhibits secretin, motilin, CCK

Opens sphincters
How does a VIPoma present?
Watery diarrhea
How does a somatostatinoma present?
Constipation
What are the hormones with disulfide bonds
PRL
Insulin
GH
Inhibin
Which hormones have the same alpha subunits?
LH, FSH, TSH
Which hormones are produced by acidophils?
GH
PRL
What hormones are produced by basophils?
FSH
LH
ACTH
TSH
What hormones are released from the posterior pituitary?
ADH (supraoptic nucleus)
Oxytocin (paraventricular nucleus)
Elevated cholesterol
Xanthomas on extensor surfaces

Increased risk for CAD
Elevated triglycerides
Xanthelasmas on eyelids and face

Increased risk of pancreatitis
Chylomicrons
Takes triglycerides from GI to liver and endothelium
VLDL
Takes triglycerides from liver to adipose
IDL
Takes triglycerides from adipose to tissue
LDL
only one to carry cholesterol
VLDL is made?
only one made in liver
IDL+ LDL
Breakdown products of VLDL
Tx for Hypercholesterolemia
Statins PASL
Pravastatin (only one renally excreted)
Atorvastatin
Lovastatin
Simvistatin

Liver enzyme check every 3 months
MOA of statins
Inhibit HMG-CoA Reductase

Most active around 8 PM. Must take at night for max efficiency
Acute recurrent Hepatitis Infection
HBcAg+, HBsAg+ (HBcAb+/-)
Recent Hepatitis Immunization within 2 wks
HBsAg+ only
Hepatitis immunization greater than 2 wks ago
HBsAb+ only
Previous hepatitis infection, now immune
HBcAb+, HBsAb+, HBsAg-
Marker of Hepatitis Infectivity
HBeAb+
Patient is non infectious re: hepatitis
HBeAg-
Patient is a chronic carrier of Hepatitis
HBsAg+ for more than 6 months
Labs in the window period of Hepatitis
HBeAb+, HBcAb+, HBsAg-
Type I hyperlipidemia
Defect of the liver type of lipoprotein lipase. Chylomicrons increased.
Type IIa Hyperlipidemia
Clathrin Pit or B100 Deficiency. LDL increased
Type IIb Hyperlipidemia
LDL/VLDL receptor deficiency. LDL and VLDL increased. This is the most common in the general population
Type III hyperlipidemia
Apo E deficiency. IDL increased
Type IV hyperlipidemia
Defect of the adipose type of lipoprotein lipase. VLDL increased.
Type V hyperlipidemia
Enzyme and receptor defect of HDL CII. Chylomicrons and VLDL increased. Assoc w/ DM
GI X-Ray Corkscrew
Esophageal spasm
GI X-Ray Apple Core
Cancer
GI X-Ray Stacked Coin
Intussusception
GI X Ray Abrupt cutoff
Volvulus
GI X Ray Bird's Beak
Achalasia
GI X Ray String sign
Pyloric stenosis
Causes of solid dysphgia
Schatzki's rings
Stricture
Cancer
Schatzki's rings
Lower esophageal webs
Causes of liquid dysphagia
Scleroderma
Achalasia
Barrerr's Esophagus
Metaplasia
Increased adenocarcinoma risk
Esophageal varices
Due to portal hypertension
Vomit blood when they rupture
Mallory-Weiss
Chronic vomiters
Tear at the LES mucosa
Boerhaave's esophagus
"Trasmural" tear of the esophagus. All layers are involved.
Achalasia (also Chagas)
Increased LES pressure
Decreased peristalsis
Loss of LES Auerbach's plexus
Bird's beak on X-Ray
Hirschprung's
Congenital lack of Auerbach's in the rectum. Newborn won't pass meconium
Zenker's Diverticulum
Above UES. Cough undigested food. Halitosis
Traction Diverticulum
Below the UES.
Plummer-Vinson Syndrome
Esophageal webs (UES)
Spoon nails
Fe Def Anemia
TE Fistula (H-Type_)
Choke w/ each feeding
Esophageal atresia w/ TE Fistula (C Type)
Vomi with first feeding
Huge gastric bubble
Duodenal Atresia
Bilious vomiting with first feeding
Double bubble
Down's syndrome
Pyloric Stenosis
Non-bilious projectile vomiting (3-4 wks old) RUQ olive sign
Choanal Atreis
Turns blue w/ feeding (smurf on a nipple) (vs TOF which turns blue when crying)
Beozar
Antrum obstruction due to mass of undigestible material
Type A Gastritis
Autoimmune
Anti-Parietal cell antibodies
Atrophic/Achlorhydria
Adenocarcinoma (Increased Risk)
Type B Gastritis
H. Pylori
Spicy Foods
Dudoenal Ulcer
Loss of barrier
Pain after meal and during the night
Relieved by eating (weight gain)
Assoc w/ H Pylori, Type O blood
Gastric Ulcer
Loss of barrier
Pain during meals
Assoc w/ NSAIDS, Type A blood
Sliding Hiatal Hernia
Fundus slides through esophageal hiatus into thorax
Rolling Hiatal Hernia
Bowel protrudes through a defect in hte diaphragm. Strangulates bowel.
Menetrier's disease
Loose protein through the rugal folds (generalized edema). Thick rugal folds
Diarrhea
>200g/day

Osmotic: Watery
Secretory: Laxative use
Inflammatory: Blood/pus
celiac Sprue
Jejunum
Wheat allergy
Villous atrophy
Anti Gluten/Gliadan antibodies
Tropical Sprue
Distal Ileum
Mesenteric Ischemia
Pain out of proportion to exam
Bugs that cause bloody diarrhea
CASES

Campylobacter
Amoeba (E. Histolytica)
Shigella
E. Coli
Salmonella
Cholangitis
Inflammation of the bile duct

Charcot's triad: Jaundice, Fever (usually w/ rigors), RUQ pain

Reynold's Pentad: Triad above + Hypotension and change in mental status
Ascending Cholangitis
common bild duct infection due to stone
Primary Sclerosing Cholangitis
p-ANCA
Bile Duct Inflammation
Beading
Assoc W/ Ulcerative Colitis
Cholestasis
Obstruction of Bile Duct
Pruritis
Increased Alk Phos
Jaundice
Cholelithiasis
Formation of Gallstones
RUQ colic
Choledocholithiasis
Gallstone obstructs bile duct
MC Gallstone
Cholesterol (invisible on X Ray)
Gallstone seen on XR
Calcium bilirubinate
Conjugated bilirubin
Water soluble
Direct
Unconjugated bilirubin
Fat soluble
Indirect
Signs of alcoholic cirrhosis
Spider angioma
Palmar erythema
Gynecomastia
Hepatorenal syndrome
build up of liver toxins causes renal failure
Xanthoma
Cholesterol buildup (elbow, achilleus)
High cholesterol leads to
Atherosclerosis
Xanthelasma
Triglyceride buildup under the eye
High triglycerides causes
Pancreatitis
Criglar Najjar Type I
Unconjugated bilirubin build up in infants
Gilbert's syndrome
Stress leads to increase in unconjugated bilirubin

Increased load saturates glucouronyl transferase
Rotor's syndrome
Bab bilirubin storage leads to increased conjugated bilirubin
Dubin Johnson
Bad bilirubin excretion leads to black liver and increased conjugated bilirubin
Hemorrhagic pancreatitis
Cullen's sign: Bleeding around the umbilicus

Turner's sign: Bleeding into flank
Tests for following pancreatitis
Amylase (sensative) breaks down carbohydrates

Lipase (specific) breaks down triglycerides
Ranson's criteria
Prognosis for pancreatitis
Ranson's criteria at presentation:
WBC>16
Age >55
Glucose > 200 (islet cells affected)
LDH>350
AST>250
Ranson's Criterial at 48 hours
BUN Increase> 5mg
Ca<8mg
HCT drops >10%
Sequester >6L fluid
pO2<60
Carcinoid syndrome
Flushing, Wheezing, Diarrhea
Currant Jelly Sputum
Klebsiella
Currant Jelly Stool
Intussusception
Familial Polyposis
100% risk of colon cancer
APC defect
Begin annual colonoscopy at 5 yo
Gardener's syndrome
Familial polyposis with bone tumors
Turbot's syndrome
Familial polyposis with brain tumors
Puetz-Jegher syndrome
Hyperpigmented mucosa
Crohn's disease
IBD w/ cobblestones, melena, creeping fat, fistulas
Ulcerative Colitis
IBD w/ pseudopolyps, hematochezia, lead pipe colon, toxic megacolon
Intussusception
Currant jelly stool, stacked coin enema
How does diverticulosis present?
Bleeds
How does diverticulitis present?
LLQ Pain
How does spastic colon present?
Intermittent Severe Cramps
How does IBS present?
Alternating diarrhea/constipation with a history of stress
How do external hemmorhoids present?
Pain on defecation
How do internal hemmorhoids present?
No pain
What is pseudomembranous colitis?
Overgrowth of C. Diff d/t normal flora being killed off (usually because of Clindamycin use)
What is Whipple's disease?
T. whippelii destroy GI tract, then spread causing malabsorption, arthralgia
What color is an upper GI bleed?
Black
weight gain
0-6m
6-12m
doubles, triples, x4?

length
0-6m
6-12m
1 y

head circum
0-6
6-12
Wt- regains birth wt by 2wks
0-6mos: 5-7 oz/wk, 2lbs/mo
6-12mos; 3-4oz/wk, 1lb/mo
5-6mos: doubles birth wt
1 year: triples birth wt
2 1/2 yrs: quadruples birth wt

Length:
0-6mos: 1in/mo
6-12mos: 1/2in/mo (add 6in)
1 year: 1 1/2 times birth length

Head circ:
0-6mos: 1/2 in/mo
6-12 mos: 1/4in/mo
What adds color to stool?
Stercobilinogen being oxidized to stercobilin
What gives urine its yellow color?
Urobilinogen being oxidized to urobilin
What is the default color of stool?
Clay colored
Dx Major Depression
5+ of the following >2/52

Sleep disturbances (early wakign)
Guilt
Energy loss
Concentration loss
Appetite loss
Psychomotor agitation
Suicidal ideation
Autism
Repetitive movements
Lack of verbal skills
Lack of bonding
Asperger's
Impaired relationships
Good communication
No mental retardation
Rett's
Girls only
Normal until 5 mo
Decreased head growth
Lose motor skills
Hand wringing
Childhood disintegrative disorder
Stops walking and talking
Selective mutism
Talks sometimes
Separation anxiety
Screams when mom leaves
ADHD
Overactivity, difficulty in school
Dysthymia
Low level sadness >2 yrs
Cyclothymia
Dysthymia w/ hypomania
Double depression
depression w/ dysthymia
Bipolar I
Depression and mania
Bipolar II
Depression and hypomania
Loose associations
Incoherent ideas, switches topics
Word Salad
Unrelated word combinations
Perseveration
repeates same words
Neologisms
makes new words
Delusion
False belief
Illusion
Misinterpreted stimulus
Hallucination
Falso sensory perception. Formication in EtOH withdrawl or cocaine intoxication
Nihilism
Thinks the world has stopped
Loss of Ego boundaries
No concpet of where I end and you begin
Cataplexy
Loss of muscle tone due to emotional stress
Paranoid personality disorder
Suspicious about everything, uses projection
Schizotypal personality disorder
Odd behavior, magical thinking; people leave them alone b/v they're weird but they will interact if approached
Schizoid personality disorder
Recluse, don't want interaction with others
Antisocial personality disorder
Lie, cheat, steal, act on impulses
Conduct Disorder
Bite. <15yo w/ traits of antisocial personality disorder
Oppositional Defiant Disorder
Bark. Defiant, noncompliant, resists authority
Histrionic personality disorder
Theatrical, sexually provocative, uses repression as a defense mechanism
Borderline personality disorder
"perpetual teenager" uses projection, acts out, self-mutilation, uses splitting as defense mechanism
Narcissistic Personality Disorder
Pompous, no empathy
Dependent personality disorder
Clingy, submissive, low self-esteem, uses regression
Obsessive-Compulsive Disorder
Perfectionist, doesn't show feelings, uses isolation
Avoidant personality disorder
Socially withdrawn, wants to fit in but fears rejection
Kleptomania
Steals for the fun of it
Pyromania
Starts fires
Intermittent explosive disorder
loses self control disproportionately to circumstances
Trichotillomania
Pulls out their own hair and eats it
Lewy Body Dementia
Stiff, visual hallucinations
Normal pressure hydrocephalus
Ataxia (magnetic gait)
Incontenence
Dementia
Korsakoff Psychosis
Alcoholic B1 deficiency
Vascular dementia
Multi-infarct
Sudden onset
uneven progression
"Stair step" decline
Huntington's Chorea
Trinucleotide repeate disorder
Chromosome 4 CAG
Personality change
Choreiform movement
Creutzfeld-Jacob
Prion induced
Die within 1 year
Corneal transplant
Pick's disease
Frontal lobe atrophy
Disinhibition
Alzheimer's
Decreased Ach in nucleus basilis of Meynert
Bad Apo E
Amyloid plaques
Tau protein
Parkinson's
Substantia nigra
Lewy bodies
Bradykinesia
Pill rolling tremor
Somatization
Psychological trigger gets them sick

Pain in 4 places, 2 GI problems
Hypochondirasis
Find in themselves the symptoms of other sick people, seek medical attention
Body dismorphic disorder
Imagined physical defect
Pain disorder
Prolonged pain not explained by physical findings
Conversion disorder
blindness, mutism triggered by a stressor
Malingering
Fakes illness for monetary gain or getting out of jail. Avoids actual treatment.
Factitious disorder
Fakes illness for attention
Seeks treatment
Factitious disorder by proxy
Fakes illness of a child to get attention
Multiple personality disorder association
Incest
Sublimation
substitute acceptable for unacceptable behavior (pt likes to fight so becomes a boxer)
Identification
Defense mechanism, acts like someone else
Displacement
Takes anger out on someone else
Idealization
Sees only good in someone despite evidence to the contrary
Transferance
Patient views Dr as parent
Countertransferrance
Dr views pt as child
Acting out
Expression of impulse (tantrums)
Regression
Immature behavior (go back in development)
Rationalization
Makes excuses for behavior in advance
Justificaiton
Makes excuses for behavior afterwards
Intellectualization
Acts like a know it all in order to aboid feeling situational emotions
Isolation
Isolate feelings in order to keep on functioning
Supression
Consciously blocks memory
Reaction formation
Unconsciously act opposite to how you feel (tears on a clown)
Undoing
Doing exactly opposite of what you used to do in order to try to right a wrong
Compensation
Doing something different from what you used to do in order to fix a wrong
Alzheimer's Drugs
AchInh---> Donezepil
NMDA Receptor BLocker: Memantine
Parkinsons Neurotransmitters
Decreased Dopamine and Decreased Ach
Parkinsons Drugs (list)
Levodopa
Carbidopa
Bromocriptine
Amantadine
Selegeline
Benztropine
Levodopa MOA
Pro drug---> Dopamine in the brain
Carbidopa MOA
Inhibits decarboxylation of levodopa in periphery
Bromocriptine MOA
Dopamine Agonist
Selegiline MOA
Selective MAO-B Inhibitor
Benztropine MOA
Antichoinergic
Typical Antipsychotics
Antagonists at D2
Haloperidol: NMS
Thioridazine: Retinitis pigmentosa
Atypical Antipsychotics
Antagonize D2 and Increase Ser

Risperidone
Olanzepine: Obesity and agranylocytosis
Clozapine: Agranulocytosis
Tricyclic Antidepressents
1) NE + Ser Reuptake Inh
2) Alpha Blocker
3) Antimuscarinic

Amitryptaline, Imipramie (used for bedwetting)
SSRI
Selective Serotonin Reuptake Inhibitors

Fluoxetine, Citalopram
MAO-I
Tyramine oxidase inhibitors

Penelzine,, Tranycypromie
Heterocyclics (list)
Trazodone
Venlafaxine
Mirtazepine
Buproprion
Trazodone
Ser Reuptake Inhibitor
Heterocyclic

Priapism
Venlafaxine
Ser, NE, Dopamine reuptake inh
Heterocyclic
Mertazepine
Heterocyclic
Alpha 2 blocker
Buproprion
Heterocyclic

Ser, NE, Nicotinic reuptake inh
Ethosuxamide
Absence Seizures in children

T-Channel Deprendent Calcium Blocker
Na Channel Blockers (anticonvulsants)
Valproic Acid
Carbemazepine (Hepatotoxic, Aplastic Anemia)
Phenytoin (Gingical Hyperplasia, lymphadenopathy)
Topiramate (also a GABA enchancer)
GABA Agonists
Gabapentin
PerGAGAlin
GABA Enhancers
Topiramate (also NA Channel BLocker)
Tiagabine
Benzo MOA
Increase the frequency of Chloride Channel Opening leading to GABA potentiation
Short acting Benzo
Alprazolam
Medium Acting Benzo
Lorazepam
Long Acting Benzo
Diazepam, Chlordiepoxide
Barbiturates MOA
Increased DURATION of CL channel opening
6 Low complement associated Nephritic Syndromes
Serum Sickness
SLE
SBE
PSGN
MPGNII
Cryoglobulinemia
Hormones with disulfide bonds
"PIGI"

Prolactin
Inhibin
GH
Insulin
Psammoma bodies
Papillary CA of Thyroid
Serous cystadenoma of Ovary
Meningioma
Mesothelioma
Jones criteria for ARF
"J<3NES"
Joints (polyarthritis)
Carditis
Nodules Subcutaneous
Erythema MArginatum
Sydenham Chorea
IgA Nephropathies
Henoch-Schonlein Purpura (HSP)
Berber's
Alports
Renal Induced Acidosis
Plasma (RTA)
Ammonia production in the CD (10% Of Urea Cycle)
Glutaminase
Carbonic Anhydrase
Hormones produced by small cell CA of Lung
ACTH (MC)
ADH
PTH
TSH
ANP
5 Causes of SIADH
"SIADH"
Small cell carcinoma
Increased ICP
A Pain
Drugs
Hypoxia
Low volume state with ACIDOSIS
RTA
Diarrha
Types of Kidney stones
Ca Oxalate (80%)
Struvite
Uric Acid
Cysteine
Pseudogout
Ca Pyrophosphate
+ Birefrengent Crystals
Rhomboid Crystals
MC older pts
Seen equally in both genders
Bladder Cancer Risk Factors
Smoking
Aniline Dyes
Benzene
Aflatoxin
Cyclophosphamide
Schistosoma haematobium
Von Hippel Lindau
Tubular Sclerosis
Causes of Papillary Necrosis
Vasculitides
AIDS
3 Anatomic Narrowings of the Ureter
Hilum
Pelvic Brim
Entrance of Bladder
Nephritic Syndrome
Hypertension
Hematuria
RBC Casts
Protein Loss <3.5 g
Nephrotic Syn
Edema
Hyperlipidemia (VLDL)
Hypercoaguable (2,7,9,10 C and S)
Decreased serum albumin
Increased urine albumin
Protein loss greater than 3.5g
MCC of UTI
1) E. Coli
2) Proteus
3) Klebsiella
Most frequent UTI in F 5-10 and 18-24
S. Saprophyticus because they stick things inside themselves
Pre-Renal Failure
Serum BUN:Creatinine > 20:1
Urine Na+ Low
Fractional Na exc <1%
Concentrated Urine
Intrarenal Failure
Serum BUN 10-15
Urine Na+ High
Fraction Na excretion >2%
Dilute urine (low specific gravity)
Renal artery stenosis
Clot in front of renal artery
GN
Inflammed glomeruli
Interstitial Nephritis
Clot off medulla
Focal Segmental GN
Clot off pieces of nephron
RPGN
Crescent Formations
MC Nephritic Disease in adults
Membranous GN
MC renal disease in blacks and hispanics
FSGN
MC renal disease in HIV/IV Drug Users
FSGN
MC Renal mass
Cyst
MC malignant renal tumor in adults
adenocarcinoma
MC malignant renal tumor in kids
Wilms Tumor
MCC of RPGN
Goodpasture's
MC Nephritic disease in kids
Minimal change disease
Oxalate stone in 3yo white F
Cystic Fibrosis
Oxalate stone in 5 yo black F
Celiac Sprue
Oxalate stone in Adult F
Whipple's Disease
Oxalate stone in adult M or F
Chron's disease
Type I RTA
High Urine pH
Metabolic Acidosis
Frequent UTI
Stones
Type II RTA
High Urine pH early....low pH late d/t depeletion of HCO3-

Hypokalemia

No carbonic anhydrase in PCT
Type IV RTA
Diabetics
Hyperkalemia
No Aldosterone (infarcted JG apparatus)
Which part of the nephron concentrates urine?
Medulla
What is Glodblatt's Kidney?
Flea-bitten kidney (contralateral side)
What is uremia?
Azotemia + Symptoms
What is azotemia?
Renal failure
What is nephritic kidney disease?
Protein loss <3.5
What is nephrotic kidney disease?
Protein loss >3.5

Massive proteinuria and lipiduria
What is seen in RPGN?
Crescents
What is post strep GN?
Subepithelial humps
What is interstitial nephritis?
Urine eosinophils (drugs), toxins
What is lupus nephritis?
Glomerular destruction
Autoimmune complexes
ds-DNA
What is MGN (Membranoglomerulonephritis)
Deopsition
What is MPGN?
Tram tracks (type II)

Low C3
What is minimal change disease?
Kids (up to age 20)
Fused foot processes
Loss of charge barrier
What is FSGS? (focal segmental glomerulosclerosis)
HIV Patients
What are the vasculitides with low C3?
PMS is Salt Lake City
Post Strep GN
MPGN Type II
SBE
Serum Sickness
Lupus
Cryoglobulinemia
What is the MCC of kidney stones?
Dehydration
What is the most common type of kidney stone?
Calcium pyrophosphate (oxylate)
What type of kidney stones have coffin lid crystals?
Triple phosphate
What type of kidney stones have rosette crystals?
Uric acid
What type of kidney stones have hexagonal crystals?
Cysteine
What type of kidney stones have envelope or dumbbell shaped crystals?
Oxalate
What disease has aniridia?
Wilm's Tumor
What is phimosis
Foreskin scarred at penis head
What is paraphimosis?
Foreskin scarred at penis base
What is urge incontinence?
Detruso spasticity leads to small bladder volume
What is stress incontinence?
Weak pelvic floor muscles (estrogen effect). Urogenital diaphragm.
What is overflow incontinence?
Cannot completely empty bladder
What structure in the GU system have one way valves?
Urethra
Ejaculatory duct
What has WBC casts?
Nephritis
What has WBC casts ONLY?
Pyelonephritis (sepsis)
What has WBC casts + eosinophils?
Interstitial nephritis (allergies)
What has WBC casts plus RBC casts?
Glomerulonephritis
What has fat casts?
Nephrotic syndrome
What has waxy casts?
Chronic renal failure
What has tubular casts?
ATN (acute tubular necrosis)
What has muddy brown casts?
ATN (acute tubular necrosis)
What has hyaline casts?
Normal sloughing
What has epithelial casts?
Normal sloughing
What has crescents?
RPGN
How do you measure afferent renal function?
Creatinine (or inulin)
How do you measure efferent renal function?
BUN or PAH
What is pre-renal failure?
Low blood flow to kidneys (BUN:CR> 20:1)
What is intrarenal failure?
Damaged glomerulus BUN:CR<20:1
What is post renal failure?
Obstruction
What is the job of the proximal tubule?
Reabsorb 60-80% of everything filtered
What is the job of the thick descending limb?
Reabsorbs water
What is the job of the thick ascending limb?
Make the concentration gradient by reabsorbing Na, K, Cl, Mg, Ca without water
What is the job of the early distal tubule?
Concentrate urine by reabsorbing NaCl
What is the job of the late distal tubule and collecting duct?
Final concentration of urine by reabsorbing water. Excretion of uric acid and make new HCO3-
What does the macula densa do?
Measures osmolarity (Na+)
What does the J-G aparatus do?
Measures volume
What is Fanconi's syndrome?
Old tetracycline use- destroys PCT

Urine phosphates, glucose, amino acids
What is Bartter's syndrome?
Defective triple transporter. Decreased Na, Cl, K but normal BP
What is psychogenic polydypsia?
Dilute urine due to excess water intake
What is central pontine myelenosis?
Due to correcting na_ faster than 0.5mEq/hr
Causes of widened S2
Increased pO2
Increased volume in R vent
Blood transfusion
Supplemental O2
Pregnancy
IV fluids
ASD (fixed split)
Deep breating
AVMs
Machinery murmur

Heart: PDA
Elbow: Dialysis Fistula
Brain: Von Hippel Lindau
Lungs: Oslet-Weber-Rendu
Heart block clue
Pain with normal heart rate

HR should increase by 10 bpm for every 1 degree increase in temperature
Maximum sinus rate
220-age in years
P wave Ions
Ca++
QRS complex ions
Na+
ST interval ion
Ca++
T wave ion
K+
U wave ion
Na+
MC non cyanotic congenital heart disease
VSD
ASD
PDA
Coarctation of Aorta
Pansystolic murmur
Mitral regurg
Tricuspid regurg
VSD
MI- Enzymes
Troponin I- Appears 2 hrs, Peaks 2 days, gone 7 days

CKMB: Appears 6 hrs, peaks 12 hours, gone 2 days

LDH: Appears 1 day, peaks 2 days, gone 3 days
P Wave
Atrium

Phase 0
PR Interval
AV node

Phase 2
Q wave
Septum

Phase 2
R upstroke
Anterior wall

Phase 2
S downstroke
Posterior wall

Phase 2
ST interval
Ventricle

Phase 2
T wave
Ventrucle

Phase 3
U Wave
Ventricle

Phase 4
What organs have resistence in series?
Liver, Kidney
What organ has the highest AV-O2 difference at rest?
Heart
What organ has the highest AV-O2 different after exercise?
Muscle
What organ has the highest AVO2 difference after a meal?
Gut
What organ has the highest AVO2 different during an exam?
Brain
What organ has the lowest AVO2 difference?
Kidney
Where does a type A thoracic dissection occur?
Ascending aorta

(cystic medial necrosis, syphillis)
Where does type B thoracic aortic dissection occur?
Descending aorta

(Trauma, atherosclerosis)
What layers does a true aortic aneurysm involve?
Intima and media
What layers does a pseudo aortic aneurysm involved?
Intima and media
What vessel has the thickest layer of smooth muscle?
Aorta
What vessels have the most smooth muscle?
Arterioles
What vessels have the largest cross sectional area?
Capillaries
What vessel has the highest compliance?
Aorta
What vessel has the highest capacitance?
Veins and venules
What stain is used to see amyloidosis?
Congo Red (apple green birefrengence
What is hemochromatosis?
Fe Deposition in organs, hyperpigmentation, arthritis, DM
What is cardiac tamponade?
Pressure equalizes in all 4 chambers

Quiet precordium

No pulse or BP

Kussmahl's sign

Pulsus paradoxus (Decrease in systolic pressure on inspiration)
What is a transudate?
Effusion of mostly water

Too much water: Heart failure, renal failure

Not enough protein: Cirrhosis, Nephrotic syndrome
What is an exudate?
Effusion of mostly protein

Purulent: Bacteria
Hemorrhagic: Truama, Cancer, PE
Fibrinous: Collagen vascular disease, Uremia, TB
Granulomatous: Non Bacterial
What murmur has a watterhammer pulse?
AR
What murmur has pulsus tardus?
AS
What cardiomyopathy has pulsus alternans?
Dilated cardiomyopathy
What disease has pulsus bigeminus?
IHSS
What murmur has an irregularly irregular pulse?
A fib
What murmur radiates to the carotids?
AS, AR
What murmur radiates to the axilla?
MR
What murmur radiates to the back?
PS
What disease has a boot shaped X-Ray?
Right ventricular hypertrophy
What disease has a bananna shaped X-Ray?
IHSS
What disease has an egg shaped X-Ray?
Transposition of the great arteries
What disease has a snowman shaped X Ray?
Total anomolous pulmonary venous return
What disease has a 3 shaped xray?
Aortic coarctation
What is Osler-Weber-Rendu?
AVM in lung, gut, CNS. Sequesters platelets leading to telangiectasias
What is Von Hippel Lindau?
AVM in head, retina (Increased risk of renal cell CA)
When do valves make noise?
Closure
What valves make noise at the start of systole?
M & T (S1)
What murmurs occur during systole?
Holosystolic (pansystolic): MR, TR, VSD

Ejection: AS, PS, HCM
What are the diastolic murmurs?
Blowing: AR, PR
Rumbling: MS, TS
What valves make noise at the start of diastole?
A&P (S2)
What murmurs are continuous?
PDA, AVM
What has a friction rub while breating?
Pleuritis
What has a friction rub while you hold your breat?
Pericarditis
What does a mid-systolic click tell you?
MVP
What does an ejection click tell you?
AS, PS
What does an opening snap tell you?
MS, TS
What does S2 splitting tell you?
Normal on inspiration b/c pulmonic valve closes later
What does wide S2 splitting tell you?
Increased O2
Increased RV volume
Delayed PV opening
What does fixed wide S2 splitting tell you?
ASD
What is Cor Pulmonale?
Pulmonary HTN leading to RV failure
What is Eisenmenger's?
Pulmonary HTN leading to a reversal L-R to R-L shunt
What is transposition of the great arteries?
Aorticopulmonary septum did not spiral
What is tetraolgy of Fallot?
Overriding aorta
PS (prognostic)
RV hypertrophy
VSD (L to R shunt)
What is truncus arteriosus?
Spiral membrane did not develop (neural crest origin)

One A/P trunk (mixed blood)
What is Epstein's anomaly?
Tricuspid sits very low (large R atria)

Teratogenic effect of lithium
What is cinchonism?
Hearing loss, tinnitus, thrombocytopenia