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1082 Cards in this Set

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Alexander the Great refused to let his troops eat fish due to this toxin; Captain William Bligh described symptoms of this toxin among his sailors on an expedition in 1789.
Ciguatera (mostly reef fish)
Most common fish food poisoning in tropical coastal regions;
Ciguatera; Ciguatera poisoning accounts for more than half of the fish-related foodborne disease outbreaks in the United States
Symptoms of ciguatera toxin
GI then neurologic
In one highly publicized case, 26 employees developed this toxicity after eating blue marlin in the World Bank cafeteria in Washington, DC, in 1997
Scombroid. Caused by ingestion of histamine in fish muscle
Saxitoxin is associated with this ocean phenom.
Red tide
Consumption of saxitoxin in this type of seafood may result in perioral tingling, paralysis and resp failure

Mussels, clams, and oysters, as well as by crabs and snails. PSP (paralytic shellfish poisons) toxins (saxitoxin is most common) block sodium ion channels

Pufferfish (fugu) poisoning is caused by
tetrodotoxin
Treatment of pufferfish poisoning consists of
Supportive care and intestinal decontamination with gut lavage and charcoal. Case reports suggest that anticholinesterases such as edrophonium may be effective
INH toxicity antidote
B6
Dig toxicity
Ovine Dig Fab
cyanide toxicity
amyl nitrite (inhalation), Na-nitrite (IV), na-thiosulfate IV
which substance is metabolized to cyanide after ingestion –
nail glue remover (acetotitrile)
cyanide antidote kit
Lilly Cyanide Antidote Package
LMWH or heparin toxicity
protamine
TCA Toxicity
Sodium Bicarb
Salicylate toxicity (oil of wintergreen, peptobismol, alka seltzer)
urine alkalinization, hemodialysis
Bitter Almonds smell
Cyanide
Garlic smell
Arsenic
Pulmonary agent first used by the Germans in 1917, smells like newly mowed hay
Phosgene gas (CG)
fruity smell
acetone, isopropyl alcohol, ethanol
Iron toxicity
Deferoxamine
Lead toxicity treatment
dimercaprol (British Anti-Lewisite or BAL), calcium disodium ethylenediaminetetraacetate (CaNA2EDTA), or meso-2,3-dimercaptosuccinic acid (DMSA); avoid dimercaprol in hepatic insufficiency or peanut allergy, cautious use in renal insufficiency or HTN
Methemoglobin toxicity treatment (Fe in 3+ rather than 2+ results in inability to bind oxygen)
methylene blue
Ethylene glycol toxicity treatment
Ethanol or fomepizole
Organophosphate toxicity treatment
atropine, pralidoxime
Acetaminophen toxicity treatment
N-Acetylcysteine oral 140mg/kg loading then 17 doses of 70mg/kg q4hr
Narcotic antidote
naloxone
Benzodiazepine toxicity treatment
Flumazenil
Deadliest nerve agent known to man
VX gas
Pyridostigmine does not work as a pre-treatment for …
VX gas and GB (sarin)
Respiratory alkalosis, anion-gap metabolic acidosis, hyperpnea, tinnitus are al clinical clues of this overdose
Salicylate poisoning
Overdose with this substance typically causes an increased osmolar gap and ketosis without significant metabolic acidosis
Isopropyl alcohol
Antidote for nitrite overdose
Methylene blue
Three classes of medicines that are first-line treatment for anaphylaxis
Epinephrine, antihistamines, steroids
A patient with underlying hypertension goes into anaphylaxis that is refractory to epinephrine. In addition to standard measures, you should use this agent.
Glucagon (pt may be on a B blocker and resistant to epinephrine
Causes of clinical deterioration, lactic acidosis and altered mental status in a patient on nitroprusside
cyanide toxicity
AKA angel dust
PCP
AKA Special K or Kit Kats
Ketamine
AKA Georgia Home Boy
GHB
AKA Roffies or La Rocha
Rohypnol
Two most frequent symptoms of mild carbon monoxide poisoning
Headache and nausea
Accumulation of this gas is responsible for decompression illness
Nitrogen
Medical significance of N-acetyl-p-benzoquinoneimine (NAPQI)
Toxic metabolite of acetominophen
Intravenous treatment for cyanide poisoning
Sodium thiosulfate
Use this nomogram to assess tylenol toxicity at 4 and 24 hours after ingestion
modified Rumack-Matthew nomogram
Medical treatment for mild to moderate salicylate intoxication
Alkalinization of the urine
Treatment of choice for severe carbon monoxide toxicity with coma
Hyperbaric oxygen
Electrolyte abnormality classically associated with MDMA (3,4-methylenedioxymethamphetamine) intoxication
Hyponatremia
Delayed adverse reaction (that typically occurs 1-2 weeks after treatment) common in patients treated with antivenoms for Crotalinae bites (rattlesnakes, copperheads, and cottonmouths)?
Serum sickness
Metalloid chronic exposure associated with the hyperkeratosis pictured here as well as with a symmetric sensorimotor polyneuropathy, hepatic angiosarcoma, along with a variety of other CNS, CV, gastrointestinal, and pulmonary disorders
Arsenic
Symptoms of cholinergic excess
SLUDGE = Salivation, lacrimation, urination, defecation, Gastric Emptying; BBB = bradycardia, bronchorrhea, bronchospasm
2 drugs found in the Mark 1 kit
Atropine and 2-PAM-Cl
Of the three vesicants, this is the only one that does not cause immediate pain
Mustard gas (Lewisite and phosgene oxide cause immediate pain)
Lab findings in CN poisoning
Severe anion-gap acidosis, bright red venous blood
Optic neuritis, AG metabolic acidosis, osmolar gap from ingestion of this
Methanol
Ingestion of these 2 alcohols can cause a high anion gap
Methanol, ethylene glycol
Reason isopropyl alcohol does not have an increased anion gap
Isopropyl alcohol is converted to acetone (neutral compound)
The treatment of choice for lithium toxicity.
Hemodialysis
Red retinal veins after exposure to carbon monoxide
Jett's sign
Red as a beet, hot as a hare, dry as a bone, blind as a bat, mad as a hatter
Anticholinergic syndrome
Salivation, lacrimation, urination, defecation, GI upset, emesis
Cholinergic syndrome/organophosphate poisoning
Depressed mental status, depressed respiration, miosis
Opiate toxiciity
Depressed mental status, bradycardia, hypothermia, hypotension, pulmonary edema, areflexia
Barbiturate toxicity
CNS excitation, seizures, HTN, tachycardia, hallucinations, mydriasis
Stimulant toxicity (amphetamines, cocaine)
This neuromuscular junction disease is characterized by weakness that may improve with repetitive exercise
Lambert-Eaton
Term for a pink or yellow tint to centrifuged CSF in a patient with acute onset, severe HA
Xanthochromia
Spongiform encepholapathy in canabalistic tribes
Kuru
Flexion of the neck gives shock sensation down the spine in patients with MS (i.e. "Barber chair sign") - also seen in trauma, Behcet's disease, any transverse myelopathy or cord compression (disc, spondylarthropathy, Arnold-Chiari), Vit B12 def (sub-acute combined degeneration)
Lhermitte's sign
Three findings on exam that suggest an upper motor neuron lesion rather than a LMN lesion
Hyperreflexia, Babinski's sign, and increased muscle tone.
Wet, wacky, wobbly
Normal pressure hydrocephalus
In a patient with meningitis, massive neck flexion results in leg flexion
Brudzinki's sign
In a patient with meningitis, resistance to full extension of the knee with the hips flexed
Kernig's sign
Most common inheritied peripheral neuropathy
Charcot-Marie-Tooth (Herditary motor sensory neuropathy)
Impaired short term memory, confabulation, with normal cognition
Korsakoff's syndrome
Ipsilateral weakness, contralateral loss of pain and temperature sensation
Brown-Sequard syndrome
Confusion, ataxia, nystagmus
Wernicke's encephalopathy (triad)
Scanning speech, intention tremor, nystagmus
Charcot's triad (for MS)
Selective anterograde and retrograde amnesia in patients that have had Wernicke's
Korsakoff's syndrome
Frequent falls are associated with this particular seizure location
Frontal lobe
Lobe that is the site of 80% of partial seizures
Temporal lobe
name for stroke like symptoms following seizure
Todd's paralysis
Neurological symptoms seen first in B12 deficiency
Loss of proprioception and vibrioception
Miners of this element get Parkinson's disease
Manganese
Test associated wit NPH and shunting
Miller-Fischer test (evaluate gait before and after removing 30 cc CSF)
Cherry red spots
Tay-Sachs or Nieman Pick
Bilateral destruction of the temporal lobes that results in placidity, hypersexuality and loss of visual recognition.
kluver-bucy
plexus affected in Achalasia
Auerbach's
Plexus affected in Hirschprung's
Meyer's plexus
Rare condition that killed actor Dudley Moore
Progressive supranuclear palsy (or, Parinaud's syndrome)
This disease is similar to MS and is characterized by optic neuritis and transverse myelitis
Devic's disease
Lower plexus palsy affecting C8-T1 nerve roots
Klumpke's palsy
Protein found in Lewy Bodies (eosinophilic cytoplasmic inclusion bodies)
synuclein
Ratio of frontal horns of ventricle to maximal diameter of cranium
0.4
Confirmation of NPH criteria
Improvement of gait with 30cc removal of CSF
syndrome characterized by headaches, confusion, seizures and visual loss, common in the post transplant time period (2/2 tacrolimus/cyclosporine), with hypercalcemia or malignant HTN / eclampsia
Posterior Reversible Encephalopathy Syndrome (PRES) or Reversible Posterior Leukoencephalopathy Syndrome (RPLS)
Hypertension, bradycardia, irregular respirations seen with increased intracranial pressure
Cushing's triad
Hearing loss, tinnitus, vertigo
Meniere's disease
Ataxia, incontinence, mental status change
Normal pressure hydrocephalus
Non-drug treatment for benign positional vertigo
Otolith repositioning maneuver such as the Epley maneuver; (Dix Hallpike for diagnosis)
Diagnosis associated with acute onset of headache, vomiting, and ataxia
Cerebellar infarction or hemorrhage (accept either)
Name of condition characterized by rapidly flowing, dancing-like involuntary movements occurring in a chaotic, nonstereotypic fashion
Chorea
Syndrome characterized by frequent falls and vertical gaze paralysis
Progressive supranuclear palsy (or, Parinaud's syndrome)
Anticonvulsant drug associated with metabolic bone disease
Phenytoin
Rapidly progressive dementia in older person with prominent startle myoclonus is associated with this CSF protein
14-3-3 protein in Creutzfeld-Jakob
Name the symptom (not diagnosis) when an individual drops to the floor with complete muscle weakness after laughing
cataplexy
Diagnosis for extra-axial, calcified brain mass with overlying skull hyperostosis
Meningioma
Transient, acute memory loss lasting for minutes without loss of consciousness
Transient global amnesia
Auditory symptom associated with Bell's palsy
Hyperacusis
Most consistently effective treatment for spasmodic torticollis (cervical dystonia)
bo-tox injections
Syndrome characterized by dysautonomia, Parkinson's symptoms, corticospinal tract signs, and ataxia
Multiple system atrophy (Shy Drager)
Pupil with consensual but not direct response to light
Marcus Gunn pupil (afferent pupillary defect)
Ocular finding in hypercalcemia
Band keratopathy
Most common cause of conjunctivitis in adults
viral conjunctiviitis
Eye involvement associated with Crohn's disease
Uveitis
Most common malignant eye tumor
Melanoma
Eye finding often associated with abdominal straining
Subconjunctival hemorrhage
This physical exam finding can help differentiate iritis from benign conjunctivitis
ciliary flush
Most common presenting symptom in MS
Optic neuritis
Diagnostic procedure of choice for a patient with endophthalmitis
Aspiration and culture of anterior chamber (accept either part of answer)
Term for conjunctival edema
Chemosis
Disease associated with corkscrew conjunctival vessels
Sickle cell
Glaucoma diagnostic criteria (3)
Progressive loss of peripheral vision, high intraocular pressure, abnormal cup/disc ratio
Papilledema, high opening pressure, headache, and diplopia with a peripheral visual field loss is best treated with these medications
Acetazolamide or furosemide (corticosteroids in severe cases) for pseudotumor cerebri
Proliferation of opaque fibrovascular conjunctival tissue medial to iris
Pterygium
Unilateral large pupil with low reactivity to light and accomodation
Adie's pupil
Disease associated with "sausaging" of retinal veins
Macroglobulinemia (accept Waldenstrom's, hyperviscosity syndrome)
Adhesions that develop between the iris and lens capsule following iritis
Synechiae
Psychiatric disorder occuring commonly following stroke
Depression
Most common psychiatric disorder in women over the age of 65 years
Generalized anxiety disorder
Name of syndrome characterized by agitation, altered mental status, nausea, vomiting, diarrhea, dizziness, hypotension, fever, shivering and diaphoresis in a patient taking an SSRI and lithium
Serotonin syndrome
Syndrome characterized by the presence of four or more unexplained symptoms
Abridged somatization
Daily spiking fevers (quotidian), arthritis and an evenescent "salmon-colored" rash
Adult Still's Disease
Likely diagnosis in a 20 yo with recurrent R knee effusions and darkly pigmented fluid on joint aspiration containing hemosiderin-laden macrophages
Pigmented Villonodular synovitis
Pain at at the elbow is reproduced with the extension of the wrist against resistance
Lateral epicondylitis (Tennis elbow)
Leading cause of knee pain in pt <45
Patellofemoral syndrome
Most sensitive physical exam test to detect a patient's torn ACL
Lachman's test
Most common cause of foot pain (outpatient)
Plantar fasciitis
3 knee injuries that make up the Unhappy Triad
ACL tear, MCL tear, medial meniscus tear
In patient with RA, the name for the appearance of the index finger bent at 90 degrees
boutonniere deformity (PIP hyperflexion with DIP hyperextension)
Suspect this cause of proximal muslce weakness and elevated CK levels in a patient on chronic treatment for gout
Colchicine myopathy
4 seronegative spondyloarthropathies
Reactive arthritis, IBD-associated, Psoriatic, Ankylosing spondylitis
Infliximab and etanercept inhibit this mediator of the inflammatory response in RA
TNF-alpha
Infliximab
human/mouse TNF alpha antibody
Adalimumab
human monoclonal antibody to TNF alpha
Certolizumab
pegylated humanized TNF alpha Fab
Golimumab
human monoclonal antibody to TNF alpha
Etanercept
fusion protein with TNF receptor and IgG
3 components of Felty's syndrome
Neutropenia, RA, splenomegaly
Acute stridor and hoarseness in a patient with RA is a signal for involvement of this joint and is an emergent indication for steroids
Cricoarythenoid synovitis
This condition, known as 'pseudophlebitis,' can mimic a DVT
Ruptured Baker's cyst
2 large vessel vasculitidies
Giant cell arteritis, Takayusu arteritis
Suspect this diagnosis in a patient with active Hep B and vasculitis
PAN (polyarteritis nodosa)
Low complement levels are commonly seen in patients with these 2 types of vasculitis
Cryoglobulinemia, SLE vasculitis
Antibodies associated with systemic sclerosis
Anti-Scl 70 or anti-centromere
This antibody is associated with the absence of interstitial lung disease in patients with scleroderma
Anti-centromere
Myositis specific autoantibodies associated with interstitial lung disease, arthritis, and a hyperkeratotic rash on the hands
Antihistidyl-tRNA synthetase
Test for lacrimal function in patients with dry eyes
Schirmer test
Syndrome characterized by pain localized to the distal radius and a positive Finkelstein's test
De Quervain's tenosynovitis
What is Finkelsteins test?
MD grasps thumb and severely ulnar deviates wrist; + = sharp pain on top of forearm
Syndrome of chelitis, dry mouth, and trouble chewing and swallowing food
Xerostomia (Sjogren's syndrome)
Essential serological finding in rheumatoid vasculitis
High titers of Rheumatoid factor
Most common extra-articular manifestation of ankylosing spondylitis
Acute anterior uveitis
candlewax appearance on back x-ray
DISH (diffuse idiopathic skeletal hyperostosis)
Autoimmune disorders that comprise Mixed connective tissue disorder
SLE, scleroderma, polymyositis
Mixed connective tissue disorder antibody
anti-U1 RNP (spliceosomal component)
Systemic Scleroderma staining pattern
Nucleolar
daily fever
quotidian
Idiopathic inflammatory myopathy that most commonly affects older men
Inclusion body myositis
2 types of arthritis that affect the DIP joints
OA (Heberden's nodes), psoriatic arthritis
name for hypersensitivity seen at sites of needle sticks in patient with Behcet's syndrome
pathergy
This class of drugs is the treatment of choice in patients with HTN crisis with scleroderma
ACE-I
Connective tissue disease in which wide mouthed colonic diverticuli are pathagnomonic
Scleroderma
This rare scleroderma-like syndrome results from ingestion of contaminated L-tryptophan supplements (interstitial infiltrates, eosinophilia, skin changes)
Eosinophilia-Myalgia syndrome
Antibody associated with neonatal lupus (congenital heart block)
Anti-SSA (Ro)
The most specific autoantibody for SLE
Anti-Smith or anti-ds-DNA
Antibody associated with psychosis and depression in SLE
anti-ribosomal P
Pulmonary complication of sjogren's syndrome predisposing to lymphoma
Lymphocytic interstitial pneumonia, activation of B cells
Apthous stomatitis, uveitis, genital ulcers
Behcet's syndrome
Blue sclera, hearing loss, brittle bones
Osteogenesis imperfecta
Lupus with renal involvement (antibody)
anti ds DNA
Primary biliary cirrhosis antibody
Antimitochondrial
Goodpasture's syndrome antibody
Anti-glomerular basement membrane
Antibody associated with drug induced lupus
anti-histone antibody
Drug used to treat Familial Mediterranean fever
Colchicine (FMF characterized by paroxysmal attacks of fever and serosal inflammation)
Major cause of mortality in patients with Familial Mediterranean Fever
Secondary Amyloidosis
The most common glycogen storage disease which can be associated with pain and weakness after exercise
McArdle's disease (myophosphorylase deficiency)
Patients of Middle Eastern descent with synovitis, erythema nodosum, sterile abscesses, and recurrent aphthous stomatitis and/or genital aphthous ulcers most likely have this disease (also a/w eye inflammatory sx and cutaneous pathergy - papular rxn persisting 24-48h after needle or skin prick)
What is Behçet disease
This HLA antigen is associated with aggressive rheumatoid arthritis
HLA DR4 (RA also associated with DR1)
This ANA pattern is typically seen in mixed connective tissue disease.
speckled
It is an inherited skeletal muscle disorder characterized by a hypermetabolic state precipitated by exposure to volatile inhalational anesthetics.
What is malignant hyperthermia?
These 2 HLA antigens have been associated with anti-glomerular basement membrane glomerulonephritis.
HLA DR2 and B7
HLA antigen associateed with ankylosing spondylitis, postgonococcal arthritis and acute anterior uveitis
B27
HLA antigens associated with Diabetes Mellitus Type 1
HLA DR3, DR4
HLA antigen associated with primary sjogren and autoimmune hepatitis
HLA DR3
HLA antigen associated with 21 hydroxylase deficiency
HLA B47
HLA antigen associated with Chronic Lyme Disease
HLA DR2 and DR4
17 year old girl with DM complaining of pain in the palmar surfaces of the first three fingers, thickening of finger skin (thick and waxy) and painful shoulders
Limited joint mobility (Cheiroarthropathy)
30 year old woman with acute onset of swelling redness and pain at the base of the big toe, amorphous calcification, normal labs, repeat x-ray 2 weeks later is normal
Hydroxyapatite periarthritis
Sign for thoracic outlet syndrome (eponym)
Adson's sign
30 year old woman with nonradiating lower back pain after delivery of her third child, trinagular sclerotic area of the ileum bilaterally, normal SI joint space, absent sclerotic changes in the sacrum
osteitis condensas ilii
The autoantibody most closely associated with Wegener's granulomatosis
C-ANCA (anti-PR3)
Congenital cystic dilatation of intrahepatic bile ducts associated with frequent bile stones
Caroli's disease
Acute colonoic pseudo-obstruction
Ogilvie's syndrome
Antibody is 95% sensitive and 98% specific for primary biliary cirrhosis
Anti-mitochondrial AB
Cause of an isolated elevation of serum alk phos in an asymptomatic woman in her 3rd trimester
Increased placental alkaline phosphatase
More common than Familial Adenomatous Polyposis, this syndrome is another hereditary form of cancer
Hereditary Non-polyposis colorectal cancer (Lynch syndrome)
Upper GI bleeding after retching
Mallory Weiss tear
Stress ulcers associated with severe burns or trauma due to ischemia of the gastric mucosa
Curling's ulcers
Erosions with incarcerated hiatal hernias, seen in 5.2% of patients with hiatal hernias
Cameron lesions
Eponym for esophageal rupture
Boerhaave's syndrome
Patient's pain out of proportion to abdominal exam findings in an elderly patient
Ischemic bowel (Messenteric ischemia)
Most common cause of an acute abdomen in a pregnant patient
Acute appendicitis
Most sensitive and specific test to diagnose acute cholecystitis
HIDA scan
Suspect this in neutropenic patient with abdominal pain
Typhlitis (neutropenic necrotizing enterocolitis)
Syndrome characterized by intestinal obstruction and pneumobilia
Gallstone ileus
Syndrome characterized by narrowing of the extra-hepatic bile duct from mechanical compression by a gallstone impacted in the cystic duct
Mirizzi's syndrome
Skin condition associated with inflammatory bowel disease but whose activity does not parallel that of the bowel disease
Pyoderma Gangrenosum
Syndrome of esophageal webs and iron deficiency anemia
Plummer Vinson syndrome
In patients with esophageal cancer, preferred non-invasive diagnostic test to determine extent of disease progression within esophageal wall and regional lymph nodes
Endoscopic ultrasonography
A cause of dysphagia that can be relieved in some patients by lifting their arms over the heads or with a Valsalva maneuver
Achalasia
Best test for suspected sclerosing cholangitis
ERCP (accept MRCP)
Gastrointestinal polyps and pigmented macules around mouth and lips
Peutz-Jeghers' disease
Drug for irritable bowel syndrome associated with ischemic colitis
Alosetron (also Tegaserod)
Drug used to treat bleeding associated with hereditary hemorrhagic telangiectasia
Combination estrogen/progesterone (accept hormone therapy)
Class of drugs causing regression of polyps in familial adenomatous polyposis
NSAIDs
Typical location of perforation in acute idiopathic intestinal obstruction
Cecum
Sudden loss of vision associated with hemorrhages confined to the optic disk and macula in acute pancreatitis
Purtscher's retinopathy
Best test to differentiate pancreatic insufficiency versus small bowel mucosal disease as a cause for malabsorption
D-Xylose test
Fe/TIBC percent consistent with hemochromatosis
45%
This monoclonal antibody reduces disease activity in both MS and Crohns disease
What is natalizumab, an alpha-4 integrin antagonist?
Stool finding with intussusception
Currant-jelly stool
Barrett's esophagus is associated with this type of abnormal cell metaplasia
Abnormal intestinal columnar epithelium
Patients with T cell mediated inflammatory rxn to gluten who present with itching may have this associated dermatologic condition
Dermatitis herpetiformis
Peutz-Jeghers syndrome is associated with these malignancies
Stomach, duodenum, breast, ovary/testicular, pancreas
Minimum Child-Pugh and MELD (Cr, INR, total bili) scores to consider liver transplantation
7 and 10 respectively
Indications for steroids and pentoxifylline in alcoholic hepatitis
Discriminant function (4.6 x (PT-control) + total bili) >32 or enchepalitis without evidence of GIB or infection
Benefit of pentoxifylline in alcoholic hepatitis
Decreased hepatorenal syndrome and mortality
Hepatotoxic mushroom
Amanita phalloides
Radiographic findings in mesenteric ischemia
Submucosal hemorrhage and edema (thumbprinting)
An elevated fecal osmotic gap suggests this type of diarrhea
Osmotic diarrhea
Formula for fecal osmotic gap
Fecal osmotic gap = stool osmolality - 2(Na + K)
Adults with acquired hypogammaglobulinemia or CVID associated with recurrent sinopulmonary infections are predisposed to malabsorption secondary to infection with this organism
Giardia
A patient with hemochromatosis develops abdominal pain, fever, and diarrhea. Stool has WBC and RBC. Infection with this organism is diagnosed.
Yersinia enterocolitica
This fundoplication operation is a surgical approach for the correction of GERD
Nissen
4 extra-esophageal manifestations of GERD
cough, asthma/RAD, hoarseness/laryngitis, dental caries
a mucosal ring at the gastro-esophageal junction that may cause dysphagia
Schatzki's ring
The appropriate treatment for ulcerative colitis with high grade dysplasia
Proctocolectomy
Eponym for syndrome with ETOH induced fatty liver, high triglycerides, and hemolysis
Zieves syndrome
This hepatic mass has been associated with the use of OCP
Hepatocellular adenoma
Bile duct cancer located at the bifurcation of the right and left hepatic ducts
klatskin tumor
In patients with varices (GI), treatment with this agent can reduce future bleeds
Beta blockers
4 well recognized causes of peptic ulcer disease
H pylori, ZE syndrome, NSAIDs, Crohn's disease
Suspect this class of diarrhea in a patient with large volume diarrhea, not relieved by fasting
Secretory
Most common cause of osmotic diarrhea
lactase deficiency
Associated with Fundal involvement of gastritis
Pernicious anemia
Associated with antral involvement of gastritis
H. Pylori
Superficial ectatic artery causing massive UGIB
Dieulafoy's lesion
RUQ pain on inspiration
Murphy's sign
A diagnostic test (not antibody) that can be used to test for celiac sprue
D-Xylose test
Extracolonic manifestiatations of Crohn's
Pyoderma gangrenosum, erythema nodosum, iritis, episcleritis, aphhthous ulcers, thromboembolic events, auoimmune hemolytic anemia, chronic hepatitis, cirrhosis, sclerosiing cholangitis
Antibody test for autimmune hepatitis
Type I: antismooth muscle Type 2: anti liver/kidney microsome Type 3: anti soluble liver antigen
5 components of child pugh classification
Ascities, encephalopathy, bilirubin, albumin, PT
RUQ pain, jaundice, fever/chills
Charcot's triad
RUQ pain, jaundice, fever/chills, MS change, hypotension
Reynauld's pentad
Syndrome where the colon is found between the liver and the diaphragm
Chilaiditi syndrome
Enlarged, palpable, nontender gallbladder seen with obstruction of the common bile duct
Courvoisier's sign
Right subscapular pain due to cholelithiasis
Boas's sign
Bluish discoloration of the periumbilical region
Cullen's sign
Hiatal hernia, gallstones, diverticulosis
Saint's triad
#1 cause of liver failure in the US
Tylenol overdose
Most common cause of asymptomatic ALT elevation
Non-alcoholic fatty liver disease
Top 3 causes of hepatitis with AST and ALT elevation greater than 5000
viral, toxins, ischemia
2 drug treatment for Hepatitis C
Interferon and ribavirin
Extrahepatic manifestions of hepatitis C
Autoimmune thyroid disease, glomerulonephritis, lichen planus, porphyria cutanea tarda, mixed cryoglobulinemia, lymphoma
Finding on colonoscopy in patient abusing laxatives
melanosis coli
This is a pancreatic islet tumor which manifests as mild diabetes, cholelithiasis, and diarrhea
What is a somatatistatinoma?
Chest pain, vomiting, cervicul subcutaneous emphysema
Mackler triad
acute hepatic or chronic biliary infection caused by eating watercress
Fasciola hepatica
Name for Intradermal antigen test for hydatid disease (echinococcus granulosus or multilocularis)
Casoni
Eponym for Hepatorenal syndrome
Frerich Syndrome
Eponym for aspiration of stomach juice
Mendelson's
Urine lab used to aid in the diagnosis of intestinal carcinoid tumor
What is 5-HIAA (5-Hydroxyindoleacetic Acid)?
Two conditions with Microvesicular fatty liver
pregnancy, reyes syndrome
Lynch 1
HNPCC with colon only
Lynch 2
HNPCC with colon, ovary,breast, endometrial
Antibody associated with ulcerative colitis
P-ANCA (60-70%)
Antibody associated with Crohn's
anti-Saccharomyces cerevisiae (ASCA) in 60-70%
Treatment of Hep B
lamivudine, adefovir, telbivudine or entecavir (entacavir most potent)
Screening tests for HCC indicated in Hep B
serum AFP and hepatic US q6 months
Suspect this diagnosis in a male patient with neuronal hearing loss and renal insufficiency
Alport Syndrome (generally X linked, sometimes AR)
The most common cause of nephrotic syndrome in patients < 15 years of age
Minimal Change Disesae
Path of kidneys in patients with diabetic nephropathy
Kimmelstiel-Wilson nodules
Drug of choice for hypertensive crisis due to preeclampsia
Hydralazine
This type of RTA is assoicated with nephrolithiasis
Type I RTA (classic, distal)
Winter's formula
PCO2 = [1.5(HCO3 + 8) +/- 2
In non-diabetic adults, these are the 2 most common causes of primary nephrotic syndrome
Membranous nephropathy, FSGS
Suspect this in a patient with nephritic syndrome who presents with flank pain, macroscopic hematuria and acute worsening of their renal function
Renal vein thrombosis
5 causes of low complement GN
post infectious, SLE, cryoglobulinemia, MPGN, endocarditiis… also cholesterol emboli
Most common cause of AKI in a hospitalized patient
ATN
Marked by acute renal failure, eosinophilia and livedo reticularis
cholesterol emboli syndrome
Most likely cause of hyperkalemia in diabetic patients with mild to moderate renal insufficiency
Hyporeninemic hypoaldosteronism (accept type IV RTA)
Diagnosis associated with hypokalemia and metabolic alkalosis
Diuretic use or vomiting or Bartter's syndrome (any)
Biological drug for acute renal failure secondary to hepatitis C associated cryoglobulinemia
alpha-Interferon
Hormone results in regression of left ventricular hypertrophy in dialysis patients
Recombinant human erythropoietin
Creatinine, sex, and age-based formula to estimate glomerular filtration rate
Cockcroft-Gault formula (any part of name)
Hydrocarbon exposure is a risk factor for this pulmonary/renal syndrome
Goodpasture's syndrome
Classes of Lupus Nephritis
I Minimal Mesangial GN (normal on light, abnormal on electron) II Mesangial Proliferative nephritis - usu responds to corticosteroids III Focal Proliferative nephritis - usu responds to high doses of corticosteroids IV Diffuse Proliferative nephritis - corticosteroids + immunosuppressants V Membranous Nephritis - extreme edema and protein loss VI Glomerulosclerosis
Anion gap represents these unmeasured anions
Phosphorous, sulfate, organic acids, anionic proteins
AG in patients with Waldenstrom's (lymphoplasmocytic lymphoma)
Low
Most common cause of secondary nephrotic syndrome
Diabetes
Most common cause of acute glomerulonephritis
IgA nephropathy (Berger's disease)
Nephrotic syndrome in heroin user with AIDS
Focal segmental glomerulosclerosis
Nephrotic syndrome in patient with chronic skin popping
Secondary amyloidosis (AA)
Aminoaciduria, phosphaturia, glycosuria
Fanconi's syndrome
Hyperreninemia hyperaldosteronism, hypokalemia, metabolic alkalosis, and/or hypomagnesemia with normal BP
Bartter's syndrome (more severe) or Gittelman's syndrome (thiazide channel)
4 primary types of kidney stones
Calcium, cystine, uric acid (radiolucent), struvite
This type of glomerulopathy is seen in Hepatitis B and C
Membranous glomerulopathy
RTA with hyporeninemic hypoaldosteronism
Type IV RTA
Most common urinary analysis abnormality in a patient with SLE
Proteinuria
The first sign of bladder cancer
Hematuria
Condition associated with dysmorphic red blood cells in the urine
Glomerulonephritis
Nutrient malabsorption causing hyperoxaluria
Fat
Renal vascular disease associated with angiographic "string of beads" appearance
Fibromuscular disease (accept fibromuscular dysplasia)
Periumbilical nodule representing metastatic abdominal (usually gastric) carcinoma
Sister Mary Joseph's nodule
Roleaux formation in a patient with anemia
Multiple myeloma
Most likely etiology of anemia in a woman with an MCV < 70 but only a mild anemia
Beta thalessemia (minor)
The first and most common clnical feature of acute and chronic graft vs host disease
Skin rash
This is the factor responsible for hypercalcemia seen in patients with multiple myeloma
Osteoclast activating factor
Most common cause of cancer death in women
Lung CA
This tumor marker may be elevated in patients with pancreatic cancer
CA 19-9
This neoplastic disease is the most common paraproteinemia
MGUS
Gene mutation associated with a 50-85% lifetime risk of developing breast CA
BRCA1 or BRCA2
In addition to other findings, multiple myeloma is defined by a BM bx containing greater than this % plasma cells
10%; also presence of M spike and symptoms (CRAB)
ISS Multiple Myeloma staging criteria
What are I: Albumin GE 3.5, B2 MicroglobulinLT 3.5, III: B2 Microglobulin GE 5.5, II neither I nor III (if B2 microglobulin is 3.5 exactly than stage II)
Most common inheritied bleeding disorder
von Willebrand disease
2 most common inheritied hypercoagulable states
Factor V Leiden, PT 20210
Syndrome of AHA and ITP
Evan's syndrome
least common and typically least aggressive of the 4 myeloproliferative syndromes
Essential thrombocytopenia
The 4 myeloproliferative syndromes
CML, PV, primary Myelofibrosis, Essential thrombocytopenia
Jackie onassis died of this disease after receiving CHOP therapy
Non-hodgkin's lymphoma
Bob Marley was at increased risk for this disease, from which he died
Malignant melanoma
This brutal warrior died of a nosebleed on his wedding night in AD453
Attila the Hun
Name 5 of the hemologic emergencies
1. Acute tumor lysis syndrome 2. Hypercalcemia 3. SVC Syndrome 4. Spinal cord compression 5. Hyperviscosity syndrome/leukostasis 6. Neoplastic pericardial tamponade 7. Acute airway obstruction 8. Neutropenic fever
mechanism of action - lepirudin, bivalirudin, argatroban
Direct thromibin inhibitors; argatrobran (hepatic clearance), lepirudin (renal clearance)
Autosomal Recessive Disease resulting in deficiency of glycoprotein IIb-IIIa complexes
Glanzmann Thrombasthenia =aGGregation problem=inteGrillin function (fibrinogen receptor)
Treatment for patient with splenomegaly, TRAP+ cells, dry bone marrow aspiration
Cladribine (2-chlorodeoxyadenosine)
Etiology of anemia in a 35 year old female with myasthenia gravis and a thymoma on CXR
pure red cell aplasia
Type of lung cancer associated with gynecomastia - due to production of bHCG
Large Cell Lung CA
Hypertrophric pulmonary osteoarthropathy (HOA) is most associated with this cell type of non-small cell lung CA
adenocarcinoma
Most common acute gastrointestinal complication of radiation therapy for prostate cancer
acute proctitis
This treatment is indicated for patients with recurrent MALT lymphoma
chemotherapy or gastrectomy
This drug is more effective than pentoxifylline in improving walking distance, functional status, and quality of life for patients with claudication
Cilostazol
Most frequent cause of transient aplastic crisis in patients with chronic hemolytic anemia
Parvovirus B19
Major use of cryoprecitate is to replace this blood component
Fibrinogen
Important cause of recurrent abdominal pain in patients with paroxysmal nocturnal hemoglobinuria
Portal or mesenteric thrombosis
Disease associated with "sausaging" of retinal veins
Macroglobulinemia (accept Waldenstrom's aka lymphoplasmocytic lymphoma, hyperviscosity syndrome)
Tests for PNH
sucrose lysis test, Ham's acid hemolysis, Flow cytometry for low levels of CD55 and CD59
CBC findings in adrenal insuff
NC anemia, lymphocytosis, eosinophilia
Absence/deficiency of Gp Ib/V/IX
Bernard Soulier (vWF receptor) – will also have mild thrombocytopenia
Chipmunk facies, microcytic anemia
Beta thal major
Anemia associated with Hydrops fetalis
Hg Barts – alpha thal with all 4 alleles affected
This disease can be ruled out by testing amniotic fluid for endonuclease Mst II cleavage pattern
SS disease
Lance armstrong's cancer
GCT
Relationship between carcinogen dose and tumor induction time
Druckrey relationship
Non-nutritive megaloblastic anemia in which malignant red cell precursors are particularly evident
Di-Guglielmo disease (see M6 AML)
Congenital pure red cell aplasia
Diamond Blackfan anemia
Severe immunodeficiency, MR, predisposition to cancers due to hypersensitivity to DNA damaging agents (ie CTX)
Bloom’s syndrome
Defect in primary homeostasis, prolonged PT, mechanism for translocating PS to the platelet membrane is defective, resulting in impaired thrombin formation
Scott syndrome
3 complications of massive RBC transfusion
DIC, hypothermia, hypokalemia, hypocalcemia
Pseudo Pelger Huet anomaly
MDS or AML
Unstable Hg and oxidant stress; precipitates of denatured Hg only visible with crystal violet stain
Heinz bodies (think thallasemia, G6PD)
Diseases with target cells on blood smear (3)
Thalassemias, Liver disease, Alcoholism
disease associated with a smudge cell
CLL
Chronic hematuria, iron deficiency anemia, DVT
PNH
Testing for presence of fetal blood cells in maternal circulation
Kleihauer-Betke test
AD condition with callous formation on palms and soles, esoph papillomas, 95% chance of developing esoph SCCA by 65yo
Tylosis Palmaris
In situ breast lesion that is not invasive but has inc risk for b/l involvement
Lobular CIS
CLL ->diffuse large cell lymphoma DLBCL) +fever, wt loss, LAD
Richter’s Syndrome
Sudden appearance and rapid increase in number and size of seborrheic keratoses with pruritis
Sign of Leser trelat
Carcinoma in situ of glans penis
Erythroplasia of Queyrat
Squamous cell CA in-situ, seen in sun exposed areas
Bowens disease
MCC malignancy
Basal Cell CA
Mutant p53 allele, predisposition towards breast carcinoma, sarcomas, and brain tumors (childhood and adult neoplasms)
Li-Fraumeni Syndrome
Left axillary node assoc with metastatic dz
Irish node
Tumor arising from CBD at confluence of right and left hepatic ducts, slow growing, sclerotic
Klatskin tumor
Carinomatous metastasis from primary site high up in peritoneal cavity; may be felt through anterior rectal wall as hard shelf
Blumer’s shelf
Metastatic GI neoplasia to ovaries
Krukenburg tumor
Hemochromatosis gene
HFE gene, C282Y, H63D
MC cancers causing malig pleural or pericardial effusions
Breast, Lung, Lymphoma
MC cancers met to bone
Breast, Lung, Thyroid, Kidney, Prostate
Cancer with thrombocytosis as associated paraneoplastic syndrome
RCC
Eponym for cholestasis with RCC
Stauffer’s Syndrome
4 Paraneoplastic syndromes associated with RCC
Erythrocytosis, Thrombocytosis, Hypercalcemia, Cholestasis
3 cancers associated with erythrocytosis
RCC, hepatocellular, cerebellar hemangioblastoma
4 cancers associated with hypercalcemia
SqCLC, RCC, Ovarian CA, MM
3 paraneoplastic syndromes associated with ovarian cancer
Hypercalcemia, Cerebellar degeneration with loss of purkinje cells (anti-yo), sign of Leser Trelat
Optic atrophy, contralateral papilledema, anosmia; occ assoc w/olfactory groove meningioma
Foster-Kennedy Syndrome
Papillary Cystadenoma lymphomatosum, parotid gland involved
Warthin’s tumor
Lymphedema following mastectomy leading to lymphangiosarcoma
Stewart-Treve Syndrome
Supraclavicular adenopathy usually on left side
Virchow’s sentinel node
Rare AD syndrome characterized by multiple hamartomas
Cowden's Disease (PTEN gene); causes hamartomatous neoplasms of the skin and mucosa, GI tract (polyps), bones, CNS, eyes, and genitourinary tract. Skin is involved in 90-100% of cases, and the thyroid is involved in 66% of cases. Increased risk of breast and thyroid cancer as well as endometrial and RCC.
Favorable cytogenetics in AML
t(15;17), t(8;21), inv16, t(16:16)
Poor cytogenetics in AML
del (5q), del(7q), monosomies 5 or 7, trisomies 8 or 13, t(6:9), 3q21q26 abnormalities, 11q23 abnormaties, 12p abnormalities, 17p abnormalities, abnormalities with 3 or more genes
Heavy chain disease with infiltration of lamina propria of small intestine with lymphoplasmacytoid cells
Seligmanns Disease
Special variant of cutaneous T cell lymphoma with generalized erythroderma, periph LAD; disseminated mycosis fungoides
Sezary Syndrome (cerebriform nuclei)
Light chains in plasma cell d/o
Bence Jones proteins
(t15;17)
APL
(t9;22)
Philadelphia Chromosome
(t8;14)
Burkitt’s Lymphoma (c-myc and immunoglobulin)
Isochromosome 12
Germ cell tumors
Broken ring of lymphoid tissue located in throat
Waldeyer’s throat ring
(t14;18)
Follicular Lymphoma (immunoglobulin and bcl-2 genes)
t(11:22)
Ewing's sarcoma
(t11;14)
Mantle cell lymphoma (bcl-1 and immunoglobulin genes)
burning pain in the feet or hands accompanied by erythema, pallor, or cyanosis, in the presence of palpable pulses (common in PV)
Erythromelalgia (treat with aspirin)
Best end-point for measuring the effect of a cancer screening intervention
Cancer specific mortality
Observational studies suggest that screening mammography is useful in women who have at least this number of years of life expectancy
5 years
Metastatic solid tumor cured with bleomycin, etoposide, and cisplatin
Testicular cancer
Best drug for warm-antibody autoimmune hemolytic anemia
Corticosteroids
Hydroxyurea re-activates expression of this developmentally silenced protein
Fetal gamma globulin
Most common neurological complication of systemic cancer
Brain metastases
Serum marker that is unique for nonseminomatous testicular cancer
Alpha fetoprotein
Relapsing (cyclical) fever of Hodgkin's disease
Pel-Ebstein fever
Test used to screen for anal intraepithelial neoplasia in high risk patients
Pap smear
Vulvar lichen sclerosis predisposes to this malignant condition
Vulvar squamous cell carcinoma
Best therapy for acute chest syndrome associated with sickle cell disease
Partial exchange transfusion
Most common cause of mild, asymptomatic thrombocytopenia in pregnancy
Gestational thrombocytopenia
Best test for paroxysmal nocturnal hemoglobinuria
Flow cytometry
Drug for acute aplastic anemia
Antithymocyte globulin or cyclosporin (either)
Name for acute lower limb ischemia caused by a massive ileofemoral DVT in which the leg is painful, swollen and blue
phlegmasia cerulea dolens
The systemic malignancy most commonly associated with erythroderma
What is lymphoma (mycosis fungoides, cutaneous T-cell lymphoma, Sezary syndrome)?
This study, published in June 2006, provided definitive evidence for the adequacy of CT-pulmonary angiography in the routine diagnosis of (outpatient) pulmonary embolism
PIOPED II
Cyclophosphamide metabolite that causes bladder cancer
acrolein
Criteria for APLAS
Sapporo criteria: 1. Clinical - thrombosis (unequivocal) or pregnancy morbidity a. Thrombosis or b. Pregnancy morbidity 1) abortion after 10 weeks in a normal fetus 2) abortion prior to 34 weeks from preeclampsia, placental insufficiency or eclampsia 3) 3 abortions prior to 10 weeks not otherwise explained by chromosomal or anatomical abnormalities 2. Laboratory - anticardiolipin, anti B2-glycoprotein or lupus anticoagulant on 2 occasions > 6 weeks apart
X-linked recessive disorder is characterized by immunodeficiency, severely dysfunctional platelets, and thrombocytopenia with microthrombocytes rather than macrothrombocytes
Wiskott-Aldrich syndrome
autosomal recessive disorder presenting with mild thrombocytopenia, circulating "giant" platelets, marked platelet dysfunction, and bleeding, absence of the platelet glycoprotein (GP) Ib-IX-V,
Bernard-Soulier
autosomal dominant trait characterized by giant platelets, mild to moderate thrombocytopenia, and leukocyte inclusions
May-Hegglin anomaly
a patient with anemia, thrombocytopenia, and large amounts of schistocytes on peripheral blood smear. 3 possible causes
DIC, HUS, TTP, HELLP
Causes increased risk of thrombosis with CA
tissue factor
Patients with lupus anticoagulant will bleed only if one of these two conditions are present
Thrombocytopenia, prothrombin deficiency
MALT lymphoma is associated with this infection
H. Pylori
The malignancy that often causes spinal cord compression is relatively radioresistant
Renal cell carcinoma
Syndrome of digital clubbing, chronic proliferative periostitis of long bones, and synovitis. Often seen in adenocarcinoma.
Hypertrophic Pulmonary Osteoarthropathy (Bamberger-Marie disease)
Thyroglobulin is a tumor marker for these 2 types of thyroid cancer
Papillary and follicular
GI polyps with oral papules, associated with thyroid CA, breast CA, and ovarian cysts
Cowden's disease
2 infectious causes of tropical sprue
E coli, Klebsiella, Enterobacter cloacae
Infectious cause of diarrhea that can mimic appendicitis or Crohn's disease
Yersinia enterocolitica
Auer rods on peripheral smear
AML
Tumor marker often seen in patients with ovarian cancer
CA-125
Leukemia with TRAP positive cells and dry bone marrow
Hairy cell leukemia
Autosomal dominant condition marked by hemangioblastomas, clearcell renal cell carcinomas, pheochromocytomas, endolymphic sac tumors of themiddle ear, serous cystadenomas and neuroendocrine tumors of the pancreas, and papillary cystadenomas of the epididymis and broad ligament
von Hippel-Lindau disease
an inherited neurocutaneous disorder that is characterized by pleomorphic features involving many organ systems, including multiple benign hamartomas of the brain, eyes, heart, lung, liver, kidney, and skin
Tuberous Sclerosis
Palmar fibromatosis (sometimes refererred to as palmar fasciitis) is a rare disorder most commonly associated with this neoplasm
ovarian cancer
Deficient in hereditary spherocytosis
Spectrin
Anemia, jaundice, splenomegaly, gallstones
hereditary spherocytosis
Congenital disorder of DNA repair is associateed with early and innumerable melanoma and nonmelanoma pigmentosa
Xeroderma pigmentosa
Microstaging method for melanoma
Breslow's thickness
4 types of cutaneous melanoma
Superficial spreading, nodular, lentigo maligna melanoma, acral-lentiginous
Histologic type of cutaneous melanoma, often found in subungual regions, occuring with equal frequency among whites and non-whites
Acral-lentiginous melanoma
Adjuvant biological therapy has ben shown to imporve relapse-free and overall survival in patients who are free of disease after surgical resection of high risk melanoma
Interferon-alfa
Ptosis, meiosis, anhydrosis
Horner's syndrome
Remnants of Rathke's pouch
Craniopharyngioma
Philadelphia chromosome
CML
Causes aplastic anemia in sickle cell patient
Parvovirus B19
Tender mass in left upper quadrant due to splenic hematoma (eponym)
Balance's sign
Left shoulder pain due to splenic rupture
Kehr's sign (Kehr's sign can also refer to shoulder pain due to blood/irritants in the peritoneal cavity)
Fever, neutropenia, rash
Sweet's syndrome
Side effect of 5-FU with stocking glove paresesthia, followed by painful erythema, swelling and desquamation
palmoplantar erythrodysesthesia (Hand-Foot Syndrome)
Treatment for patient with AIHA and TTP
Plasma exchange
Max dose of anthracyclines
550 mg/m2
Elevation in WBC diff in patient with myelodysplastic syndrome
Monocytes
Factor produced by the liver that is increased in anemia of chronic disease and leads to decresased release of iron from macrophages
Hepcidin
Endocrine disorders that can lead to anemia
hypothyroidism, addison disease, hypogonadism, panhypopit (including decreased growth hormone)
Expect this mass in a patient with pure red cell aplasia
Thymoma (paraneoplastic)
anticerebellar antibodie associated with small cell cancer
Anti-Hu - antineuronal nuclear antibody Type 1
anticerebellar antibodies associated with breast cancer and directed against Purkinje cells
Anti-Yo (anti-purkinje cell antibody)
Faggot cell
AML M3 Subtype (Acute promyelocytic leukemia)
"flame cell"
Multiple myeloma
"Lacunar cell"
Hodgkin's lymphoma (usuually nodular sclerosing)
Fever, retroorbital pain, "breakbone" aches and pains in a febrile traveler
Dengue fever (flavivirus, + tourniquet test - 20 petechia/inch2, Aedes aegypti mosquito)
Fever with bradycardia (pulse-temperature dissociation), abdominal pain & "rose" colored abdominal rash
Typhoid fever (Salmonella Typhi), "nervous fever"
Hot tub rash
Pseudomonas aeurginosa
The most important prognostic factor in a patient without an underlying comorbidity who has cryptococcal meningitis
CSF opening pressure
Most common cause of acute, nonepidemic encephalitis in the US
HSV
The three tic born illness endemic to Nantucket Island, and their treatments
1. Babesiosis - IV clinda/ oral quinine, 2. Lyme - doxy, 3. Ehrlichiosis - doxy
Human granulocytic anaplasmosis organism
Anaplasma phagocytophilum
Infection in asplenic/Martha's vineyard
Babesia microti (Babesiosis)
Drug used to eradicate liver hypnozoites in patient with malaria due to P. ovale or P. vivax
primaquine ("prime the liver")
The most direct method of diagnosing primary and secondary syphilis
Darkfield microscopy
Despite treatment, this test stays positive for life in patients with syphilis
Fluorescent Treponemal antibodies
4 criteria required for the diagnosis of bacterial vaginosis
Homogeneous, thin, grayish-white discharge that smoothly coats the vaginal walls, vaginal pH greater than 4.5, positive whiff-amine test, clue cells on wet mount - need 3/4 Amsel criteria
The virus contained in the smallpox vaccine
Vaccinia virus
This antiviral medication has shown antiviral activity against smallpox in animal models and may be employed in a smallpox (variola virus, poxviridae) oubreak
Cidofovir (limited by renal toxicity)
The most feared and often fatal complication of smallpox vaccination
Vaccinia necrosum; tx with VIG (vaccinia immune globulin)
Name of triad of ipsilateral facial nerve paralysis, ear pain and vesicles
Ramsay-Hunt syndrome
The reactivation of this virus causes PML (progressive multifocal leukoencephalopathy)
JC virus (polyoma virus)
Necrotizing fasciitis of the perineal and genital fascia
Fournier's gangrene
Umbilicated pearly papules
Molluscum contagiosum
Causative organism for tinea versicolor
Malassezia furfur and globosa (also the most common cause of seborrheic dermatitis)
In a patient with AIDS, disseminated (cutaneous) infection with this organism mimics molluscum
Cryptococcus
Rectal swab from a patient with suspected disseminated gonococcal infection should be plated on this agar
Thayer-Martin agar
The virus that causes Kaposi's sarcoma
HHV-8
AKA Valley Fever
Coccidiodomycoses
AKA Rabbit Fever
Tularemia
AKA Kala Azar
Visceral Leishmaniasis
AKA River Blindness
Onchocerciasis ( Onchocerca volvulus transmitted by the black fly; tx: ivermectin)
AKA Katayama Fever
Acute Shistosomiasis (fever, lethargy, the eruption of pale temporary bumps associated with severe itching (urticarial) rash, liver and spleen enlargement, and bronchospasm)
AKA Blackwater Fever
Malaria with intravascular hemolysis, hemoglobinuria, and renal failure
Eponym for severe form of leptospirosis including renal failure, hepatic failure and/or meningitis
Weil's syndrome/disease
Vector for Leishmaniasis
Sand fly (Phlebotomous)
Vector for African sleeping sickness (Trypanasoma Brucei)
Tse Tse
Vector for Chagas Disease (Trypanasoma Cruzi)
Reduviid bug
MC roundworm infection in the US
Pinworm (Enterobius Vermicularis) - no eosinophils (no invasion)
MC roundworm infection in the world
Ascaris Lumbricoides (Largest nematode, Lung disease in Larval Stage (Loffler's),Tx: Mebendazole)
Two diseases treated by ivermectin
Onchocerciasis, filariasis
Skin lesions after wading in water
Vibrio vulnificus
Bacterial agent causing pneumonia associated with the following risk factors: bronchiectasis, daily corticosteroid therapy, and malnutrition
Pseudomonas
Infection characterized by productive cough, hemoptysis, and cavitary pulmonary lesion in a patient with pulmonary silicosis
Tuberculosis
Diagnosis suggested by a severe CAP with pancytopenia in the setting of bird exposures
Chlamidophila psitticai
Class of drug useful in the treatment of both influenza A and influenza B
Neuraminidase inhibitors (zanamavir and oseltamavir)
Method of action for amantadine
interference with a viral protein, M2 (an ion channel),[15][16] which is required for the viral particle to become "uncoated" once taken inside a cell by endocytosis.
Preferred first-line antibiotic for the pneumonic form of tularemia
Gentamicin or streptomycin
Nasal mucosal atrophy and foul-smelling crusts in the nasal passages
Ozena (klebsiella infection in atrophic rhinitis)
Gram-stain finding in expectorated sputum from a chemotherapy patient
Candida
Class of anti-influenza drugs with activity against influenza B
Neuraminidase inhibitors
The two most common bacterial pathogens associated with bronchiectasis
Pseudomonas and Staphylococcus
Name of childhood illness caused by parvovirus B 19
Erythema infectiosum (fifth disease)
Etiological agent of fish tank granuloma
Mycobacterium marinum
Cutaneous anthrax location that is an indication for IV antibiotics
Face and neck
Causative organism for this skin finding
Treponema pallidum (condyloma lata)
Triad: arthritis, dermatitis, tenosynovitis
Meltzer's triad (disseminated gonococcal infection)
Acute necrotizing ulcerative gingivitis (eponym)
Vincent's angina
Two HIV drugs that cannot be used together
AZT and d4T
Bacteremia and sepsis in splenectomized patient bitten by dog
Capnocytophaga canimorsis
HIV drug may cause a hypersensitivity reaction consisting of a generalized rash and/or flu-like illness
Abacavir
The 2 bacteria associated with bacterial endocarditis and colon cancer
Strepotoccus bovis and Clostridium septicum
Organism responsible for whipple's disease
Tropheryma whippelii
Vector for HGA
Ixodes tick
Appearance of KOH prep in a patient with tinea versicolor
spaghetti and meatball appearance
Benign, recurrent aseptic meningitis
Mollaret's meningitis
Increased sebum production in patients with acne leads to proliferation of this organism
Propionobacterium acne
Most common cause of epididymitis in sexually active men aged < 35 years old
N. gonorrhea (chlamydia second)
This HIV medication can cause BM suppression
Zidovudine
Patient with HIV with foot drop and neg MRI
mononeuritis multiplex
Rickettsial infection with no insect vector. Presents with fever, headache, myalgias, nonproductive cough, and hepatitis
Q fever (Coxiella burnetti)
Causative organism for the plague
Yersinia pestis
This protease inhibitor is associated with kidney stones
Indinavir
CT head in HIV with ring enhancing lesions
CNS toxoplasmosis or lymphoma
2 indications to use steroids in PCP
pO2 < 70 or AA gradient > 35
CDC recommended medicine for leishmaniasis
Pentavalent antimony (stibogluconate; Pentastam)
Patients with cirrhosis and sepsis following raw oyster feast - suspect this bacteria
Vibrio vulnificus
Painful genital ulcer
Haemophilus ducreyi
Disease causing clue cells ona a wet prep
Bacterial vaginosis (Gardnerella vaginalis)
Strawberry cervix
Trichomonas vaginalis
Lymphogranuloma venereum (LGV)
Chlamydia trachomatis (L1, L2, and L3 serovars)
Caused by klebsiella grannulomatosis, this uncommon disease is characterized by horrible appearing genital ulcers
Granuloma inguinale (Donovanosis)
Usual cause of traveler's diarrhea
ETEC
Enteritis with this organism is associated with Guillian-Barre syndrome
Campylobacter Jejuni
E. coli O157:H7 must be grown on this media
MacConkey-Sorbital agar
Lyme disease vector
Ixodes tick
TB vaccine name
Bacille Calmette-Guerin
Toxin from clostridium tetanus
Tetanospasm
Impetigo
Streptococcus
Rose spots
Salmonella typhi
Fever, flu-like symptoms, tachycardia, hypotension during syphilis treatment
Jarisch-Herxheimer reaction
Organism associated with chronic diarrhea and eosinophilia in an AIDS patient
Isospora Belli
Treatment for Toxoplasmosis
Sulfadiazine, Pyrimethamime, folic acid
Bullous myringitis associated with this organism
Mycoplasma pneumoniae
Mycoplasma pneumoniae may cause this hematologic abnormality
Hemolysis (60%; secondary to cold agglutinin)
Mycoplasma is most commonly treated with this antibiotic
Azithromycin
Infection that is the leading cause of adult onset seizures
Taenia solium (from eating undercooked pork; larval stage metacestode causes cysticercosis)
Tapeworm infection associated with eating undercooked beef
Taenia saginata
Tapeworm infection associated with eating fish
Diphyllobothrium latum
2 medications used in the treatment of measles
Ribavirin and Vitamin A
1st disease
Rubeola
2nd disease
Streptococcal spotted fever
3rd disease
Rubella
4th disease
Filator-Duke's disease
5th disease
Erythema infectiosum (Parvo)
6th disease
Exanthem Subitum (HHV 6)
Koplik's spots
Measles
Rocky mounted spotted fever organism
Rickettsia rickettsii
Horder spots
Psittacosis
Jugular vein thrombophlebitis secondary to Fusobacterium
lemierre's syndrome
Eponym for posterior cervical lymphadenopathy in Trypanosomiasis
Winter bottom sign
Rash in disseminated pseudomonas
Ecthyma Gangrenosum
HIV drug associated with nightmares
Efavirenz
HIV drug associated with Fanconi's syndrome
Tenofovir
Most common cause of eosinophilic meningitis in the world
Angiostrongylus Cantonensis
Strain of e coli causing recent outbreak in 2010
O145
findings on exam suggestive of severe aortic insufficiency
severity proportional to DURATION of murmur (except in acute and severe late disease)
Rapid rise and fall of pulse (AR sign)
Corrigan’s (or Watson's) water-hammer pulse
A systolic and diastolic bruit heard when the femoral artery is partially compressed (sign of AI)
Duroziez’s sign
A pistol shot pulse (systolic and diastolic sounds) heard over the femoral arteries, esp with distal compression (sign of AI)
Traube’s sound
Pulsating cervix (sign of AI)
Shelly’s sign
Visible pulsations of the retinal arteries and pupils (sign of AI)
Becker’s sign
Splenic pulsation (sign of AI)
Gerhard’s sign
Head-bobbing with heartbeat (sign of AI)
de Musset’s sign
Systolic pulstations of the liver (sign of AI)
rosenbach's sign
More than a 15 mmHg decrease in diastolic blood pressure with arm elevation from the value obtained with the arm in the standard position. (AI sign)
Mayne's sign
Popliteal cuff systolic pressure exceeding brachial pressure by more than 20 (60?) mmHg (AI sign)
Hill's sign
Systolic pulsation of uvula (AI sign)
Mueller’s sign
Subungal capillary pulsations (AI sign)
Quincke’s pulses
findings on exam suggestive of severe aortic stenosis
pulsus parvus et tardus, late peaking murmur, inaudible A2, single or paradoxically split S2, LV heave, S4
Pulse of severe aortic stenosis
Pulsus parvus et tardus
echo classification of AS
1.) gradient: mild < 25, moderate 25-40, severe >40; 2.) Velocity > 4 m/s (severe) 3.) AoVA (cm2): mild 1.5-2, moderate 1.0-1.5, severe < 1.0
hematologic abn a/w more severe AS
acquired von Willebrand disease (destruction of vWF by shear forces)
Notching in the ascending limb of the S wave in leads V3 and V4 in a pt with MI and known LBBB
Cabrera's sign
Notching of the ascending limb of the R wave in lead V5 or V6 in a pt with MI and known LBBB
Chapman’s sign
A clenched fist pressed against the center of the chest in a patient with angina
Levine’s sign
Which finding is most highly suggestive of significant ischemic heart disease on exercise ECT testing
An S3 heart sound heard during the test
Duke Treadmill Score
Exercise time - 5 (ST segment deviation) - 4xangina (1 nonlimiting, 2 limiting) Low GE 5 Moderate -10 to +4 High LE -11
Pleuritic chest pain alleviated in pericarditis when bending to a chest on knee position
Pins’ sign
Exaggeration of pulmonary sounds in acute pericarditis.
Warthin’s sign
Most common cancers causing Pericardial effusions
Lung, breast, NHL, RCC
Dullness at the angle of the left scapula caused by pericardial effusion
Ewart’s sign
A paradoxical increase in venous distention and pressure during inspiration seen in constrictive pericarditis
Kussmaul’s sign (sign of RV dysfunction, also seen in effusion w/ tamponade, restrictive CMP, RV failure/infarct, tricuspid stenosis)
Physical exam finding in hypertrophic cardiomyopathy, this ‘sign’ is characterized by a large atrial kick, a sustained left ventricular impulse, and an S3.
The triple ripple
Pulse of HOCM
Pulsus bisferians
The jugular venous pulse wave caused by bulging upward of the closed tricuspid valve during RV contraction
C-wave
Brockenbrough phenomenon
Paradoxically diminished pulse occurring after a premature beat in HOCM
Severe left ventricular failure EKG finding
Pulsus alternans
cyclic crescendo-decrescendo respiratory effort and airflow during wakefulness or sleep (associated with heart failure)
Cheyne-Stokes
HACEK
Haemophilus (Haemophilus parainfluenzae, Haemophilus aphrophilus, and Haemophilus paraphrophilus)[3] Actinobacillus actinomycetemcomitans (now called Aggregatibacter actinomycetemcomitans) Cardiobacterium hominis Eikenella corrodens Kingella kingae
Name these pathognmonic, (typically) distal, nontender, erythematous/hemorrhagic, macular/nodular lesions and associated condition
Janeway lesions; infective endocarditis
Name these painful, red lesions on the palms of the hands and soles of feet c/w immune complex deposition and the classic associated disease states
Osler's nodes; infective endocarditis; also seen in SLE, maranatic endocarditis, disseminated gonococcal infection, infected arterial catheters (distal to catheter)
JONES criteria
Joints, Carditis, Nodes (subcutaneous), Erythema marginatum, Sydenham's chorea
Antibiotics for endocarditis prophylaxis
Amoxicillin/Ampicillin 2 grams Clindamycin 600 mg PO/IV
The 2 bacteria associated with bacterial endocarditis and colon cancer
Strepotoccus bovis and Clostridium septicum
Activation of receptors in the atria, great veins, and left ventricle may lead to this reflex causing neurocardiogenic syncope
Bezold-Jarisch reflex
Venous waveform letters
a = atrial contraction c = closure of TV with early ventricular contraction - bulging of TV back into RA x = atrial relaxation, downard movement of ventricle during contraction v = venous filling against a closed valve y = opening of TV
Lenegre-Lev syndrome
An acquired complete heart block due to idiopathic fibrosis and calcification of the electrical conduction system of the heart (His bundle, or bundle branches with corresponding conduction blocks). Both sexes affected; onset over 50 years of age. It is often described as senile or sclerodegenerative degeneration of the conduction system.
anti-hypertensive that raises ICP (avoid in neuro HTN emergency)
nitroprusside
The ejection fraction or systolic left ventricle internal diameter used as in indication for surgical intervention in severe mitral regurgitation
Left ventricular ejection fraction < 60% or left ventricular internal diameter in systole > 45 mm
dig toxicity
digi FAB,
These 2 agents are first line anti-anginal therapies for patients with cocaine induced angina an EKG changes
Nitroglycerin and calcium antagonists
EkG findings in a patient with a low body temperature
Osborne waves
ECG changes found in patients with massive PE that may correlate with more severe RV strain
Anterior T wave inversions
Consider witholding calcium as a treatment of hyperkalemia in patients on this drug
Digoxin
ECG changes with hypercalcemia
shortened QT interval
Abnormality associated with fixed splitting of S2
ASD
Diastolic murmur with opening snap
Mitral stenosis
Eponym applied to physical examination sign describing an increased intensity of a heart murmur during inspiration
Carvallo's sign
Diagnosis associated with equalization of diastolic pressures in right atrium, right ventricle, wedge pressure, and left ventricle
Tamponade or constrictive pericarditis
Drug reduces risk for aortic valve replacement for chronic aortic regurgitation
Nifedipine
Eponym associated with systolic plethora and diastolic blanching in the nail
Quincke’s pulse
Most important factor determining prognosis following myocardial infarction
Left ventricular ejection fraction
Coronary artery most often responsible for ischemic papillary muscle rupture
Posterior descending artery (accept RCA)
Diagnosis associated with bradycardia and variable intensity of S1
Complete heart block
Presence of this drug is a contraindication to calcium gluconate in the treatment of hyperkalemia
Digitalis
Drugs used for "pill-in-the-pocket" treatment of atrial fibrillation
Flecainide and propafenone
Cardiac auscultatory finding associated with acute ischemia that disappears with relief of the ischemia
Mitral regurgitant murmur (accept holosystolic murmur), paradoxical splitting of S2, and an S4 (any one answer accepted)
Phase of respiration when pericardial friction rubs are best heard
Inspiration
Meaning of each of the 1st three letters in NBG pacing code
Chamber paced, chamber sensed, response to sensing
When placing a temporary TV pacer, these are the 3 things that you must set on the device
HR, output (mA), sensitivity
Result of placing a magnet over a DDD pacemaker
Failure of sensing (function asynchronously), reverts to factory settings
Feared complication that can occur in asynchronous (AOO) pacing
R-on-T phenomenon causing Torsades
Syndrome charactererized by long QT and congenital deafness
Jerville-Lange-Nielson Syndrome
Preferred treatment for RV-outflow tract ventricular tachycardia
Catheter ablation
S2 in a patient with LBBB
Paradoxical splitting
Refractory tachycardia in a patient on theophylline
Multifocal Atrial Tachycardia (MAT)
5 causes of PEA
Hypovolemia, Hypoxia, Hydrogen ion (acidosis), Hyper/hypokalemia, Hypothermia, Hypoglycemia Tablets or Toxins, Trauma, Tension Pneumo, Tamponade, Thombosis (coronary), Thrombosis (pulmonary)
Sensitivity of TTE/TEE
65%/>90%
An appropriate antiarrhythmic for a fib in patients with CRF
quinidine
Single most common cause of culture negative endocarditis
Prior antibiotic use
Feared complication of inserting a PA catheter in a patient with LBBB
RBBB (trifascicular block, LBBB + RBBB)
Causes of high output heart failure
Thyrotoxicosis, anemia, AV fistula, Paget's, Carcinoid, thiamine deficiency (Beriberi)
Valvular lesion that occurs in 70% of patients with coarctation of the aorta
Bicuspid aortic valve
Classic EKG findings in patients with intracerebral hemorrhage
Diffuse T wave inversions, prolonged QT, bradycardia
Cardiac drug causing pneumonitis, thyroid dysfunction, and proarrhythmia
Amiodarone
ASD leading to right to left shunting
Eisenmenger syndrome
Most common adult congenital heart disease
Bicuspid aortic valve
Most common cyanotic congenital heart disease
Tetrology of Fallot
Disorder characterized by transient dysfunction of the apical portion of the LV, with compensatory hyperkinesis of the basal walls, prducing ballooning of the apex with systole in the absence of coronary artery disease
Takotsubo cardiomyopathy
JVD, decreased heart sounds, hypotension
Beck's triad (cardiac tamponade)
3 causes of holosystolic murmur
MR, TR, VSD
short PR with no delta wave
Lown-Ganong-Levine
Long QT (AD; without deafness)
Romano Ward
Association between bleeding from gatrointestinal angiodysplasia and severe aortic stenosis which may resolve with aortic valve replacement; may also be explained by acquired type Iia von Willebrand's syndrome
Heyde's syndrome
Chronic ergotism (historically from consumption of rye contaminated with ergot fungus); characterized by intense burning pain of the feet, hands, and whole limbs due to vasoconstrictive properties of ergot
st anthony's fire
Sydenham's chorea (eponym)
st vidus's dance
Aortic insufficiency like murmur in early diastole found in anemia
Cabot-Locke
Rapid xy descent
Constrictive pericarditis
Left vocal cord paralysis secondary to LAE secondary to mitral stenosis
Ortner's syndrome
Valvular abnormality associated with Ankylosing spondylitis
Aortic regurgitation
RBBB, persistent ST elevations in leads V1 and V2 without evidence of structural heart disease
Brugada's syndrome
High Risk Cardiac contraindications to pregnancy
Eisenmenger's, severe pulm HTN, complex cyanotic heart dz, marfan's with aortic root or valve involvement, severe AS, aortic or mitral valve dz with EF < 40%, NYHA class III or IV, prior peripartum cardiomyopathy
Continuous LTOT would be indicated with a pO2 56-59 in these patients
dependent edema, cor pulmonale with p pulmonale on ECG (>3mv in inferior leads), or Hct>56
Findings comprising Bergman's Triad and associated disease state
petechia, dyspnea, MS changes; a/w Fat Emboli syndrome
Eponym for high-pitched, blowing murmur that may be found in a patient with pulmonary regurgitation resulting from pulmonary HTN
Graham-Steell
Endocarditis with cancer
Marantic Endocarditis
2 possible causes of hypercalcemia in a patient with a high PTH-intact level
1. primary hyperparathyroidism, 2. Familial Hypocalciuric Hypercalcmia, Lithium use
The drug used to treat hyperthyroidism in pregnancy, is associated with a small risk of agranulocytosis
PTU
Hypotension, gingival and palmar crease hyperpigmentation is seen in this disease
Addison's disease (primary adrenal insufficiency)
Most common type of secretory pituitary mass
Prolactinoma
Failure of lactation following a complicated C-section delivery
Sheehan's syndrome
Sudden onset of severe headache, visual changes and hypotension in a patient with a known pituitary macroadenoma
Pituitary apoplexy (pituitary hemorrhage)
Hemochromatosis, when involving the pituitary, most commonly results in deficiency of this pituitary hormones
Gonadotropin deficiency (LH, FSH)
President George H. Bush
Possible TSH-receptor antibodies
According to the WHO, a T score of this value is the definition of osteoporosis
T-score < or = to 2.5
Suspect this dx in a male with premature osteoporosis and loss of libido
Hypogonadism
Most important initial therapy in patients with significant hypercalcemia
Volume expansion
Suspect this diagnosis in a patient with significant diuretic induced hypokalemia
Primary hyperaldosteronism
95% of cases of congenital adrenal hyperplasia are due to deficiency of this enzyme
21-hydroxylase deficiency
2 most common etiologies seen in single adrenal masses
Adrenal Adenoma Metastasis to adrenal glands
3 drugs used to treat a patient in thyroid storm
Beta blockers, PTU/Methimazole, iodine, steroids
Jane Austen is believed to have died of this, brought on by TB of a particular organ system
Primary adrenal insufficiency (Addison's disease)
Best test to distinguish thyroiditis from factitious hyperthyroidism in a patient with a low RAIU
thyroglobulin
Osteitis fibrosa cystica - chronic hyperparathyroidism eponym
Von Recklinghausen disease of the bone
Diabetic syndrome of symmetric proximal leg weakness and pain
Diabetic amyotrophy
Preferred imaging test for insulinoma
Endoscopic ultrasonography
Sign associated with contraction of the facial muscles after tapping facial nerve
Chvostek's sign
Facial plethora as a sign of increased thoracic inlet pressure/obstruction with the raising of the patient's arms
Pemberton's sign; can be caused by retrosternal thyroid gland
This hormone deficiency is associated with kallman's syndrome
Gonadatropin-releasing hormone
Non-insulin hormone responsible for storing body fat
Leptin
Severe hypertension, metabolic acidosis, hypokalemia and suppressed plasma renin activity and plasma aldosterone
Liddle's syndrome
Metabolic disease that is associated with patient smelling like putrid fish
Trimethylaminuria
Acromegaly screening/confirmatory tests
IGF-1 (somatomedin C), 100 gram glucose load challenge
Most sensitive test for primary adrenal insufficiency
ACTH stim test
Screening test for patient with glucose intolerance, several skin tags, and who on colonoscopy has multiple polyps
IGF-1 (Glucose tolerance test is confirmatory)
PCOS eponym
Stein Leventhal syndrome
Order this test to follow a patient with secondary hypothyroidism
Free T4
Thyroid cancer associated with MEN2
Medullary thyroid cancer
Feared complication of PTU and methimatazole
Agranulocytosis
The 2 tests that distinguish Grave's disease, factitious thyrotoxicosis and subacute thyroiditis
RAIU and TG (or ESR)
In a patient with subacute hypothyroidism, this test is the best predictor if overt hypothyroidism will develop over time
Anti-TPO antibodies
Adrenal insufficiency may have these CBC abnormalities
eosinphilia, normocytic anemia, lymphocytosis
Polyglandular autoimmune syndrome I
Parathyroid insufficency, adrenal insuficiency, mucocutaneous candidiasis
Hyperkalemia is seen in this type of adrenal insufficiency
Primary adrenal insufficiency
Polyglandular autoimmune syndrome II
adrenal insufficiency,autoimmune thyroid disease, Diabetes Mellitus I
Polyglandular autoimmune syndrome III
autoimmune thyroiditis with another autoimmune disease that is not autoimmune adrenalitis
This substance can give hypokalemia and HTN
Licorice
Genetic disorder affecting the Na channel in the renal tubule
Liddle's syndrome
AB present in Hashimoto's
Thyroid peroxidase (TPO) antibody
Components of Sipple's syndrome
Medullary thyroid cancer, pheochromocytoma, hyperparathyroidism
Components of Wermer syndrome
Hyperpara, hyperpit, pancreatic tumor
Hyperpigmentation in adrenal insufficiency is caused by this
ACTH
Hyperthyroidism following iodine contrast
Jod-Basedow phenomenon
Sudden exposure to excess serum iodide inhibits organification of iodide, thereby diminishing hormone biosynthesis
Wolf-Chaikoff effect
Genetics of MEN1
Chromosome 11, MEN 1 gene
Genetics of MEN2
Chromosome 10, ret-proto oncogene
Hyperthyroidism drug not given to women
Methimazole (causes aphasia cutis in newborns)
3 endocrine disorders that can cause carpal tunnel syndrome
Acromegaly, hypothyroidism, diabetes
First manifestation of iodine deficiency
Goiter
Most common thyroid cancer
Papillary carcinoma
Found on FNA of papillary thyroid cancers
Psammoma bodies
2 hormones from posterior pituitary
oxytocin and ADH
Hypogonadic hypogonadism (Low GnRH with low FSH and LH), anosmia, and color blindness
Kallman syndrome
Antibody to test in Diabetes Type I
Glutamic acid decarboxylase
Diabetes, hirsutism, post-menopausal women
Achard-Thiers
Disappearing bone disease
Gorhams Disease
Osmolality equation
2Na +Glucose/18 + BUN/2.8
Osmolality when thirst begins
295
Time of peak for ACTH
3-4 am
Two hormones controlling GH
GHRH, Somatostatin
Two hormones controlling TSH
TRH, Somatostatin
Most common cause(s) of pituitary macroadenoma
lactotrophs, gonadotrophs
Most common presentation of gonadotroph tumo
non-functional mass (can test for alpha subunits to help diagnose; TRH stimulation test can also be used)
Treatment for empty sella syndrome
usually none - 90%+ function normally
Threshold of prolactin when prolactinoma very likely
>200
PRL Levels correlate with tumor size in macroadenomas - true or false
TRUE
Treatment for prolactinoma
Bromocriptine (safe in pregnancy) and cabergoline (better tolerated, more expensive)
Contraindications to cabergoline
known lung, heart valve, and retroperitoneal fibrotic disease (Parkinson's at increased risk for diseased heart valve)
Postpartum infarct of pituitary that results in anterior hypopit and sometimes central diabetes insipidus
Sheehan's syndrome
Other causes of pituitary mass
craniopharyngioma, cns lymphoma, 1% metastatic cancer (Breast and lung)
Definition of pituitary incidentaloma
<10 mm; asymptomatic - requires work-up for PRL only
Variable onset with severeheadache, N/V, meningismus, vertigo, visual defects, fluctuating consciousness
Pituitary apoplexy (pituitary hemorrhage) - can occur immediately or over 1-2 days
Diabetes mellitus, hypogonadism, large hands and feet, large head with a lowering brow and course features
acromegaly
Most common endocrine conditions that cause carpal tunnel syndrome
DM, acromegaly, hypothyroidism
Screening and confirmatory test for GH excess
IGF-1 (>3 u/ml), 100 gm oral glucose suppression test
Treatment for somatotroph adenoma
Always treat even if symptomatic -> transphenoidal surgery, irradiaiton. Bromocriptine can be used paradoxically. Can also use octreotide/lanreotide or pegvisomant (GH R antag)
What can mimic partial nephrogenic DI
polydipsic DI
Alternate treatment choices for DI
Desmopressin, Thiazide diuretics
adipsic hypernatremia
occurs when thirst and adh osmoreceptors are damaged - hypernatremic dehydration without thirst
Treatment for refractory SIADH
Demeclocycline (adverse rxn: photosensitivity and nephrotoxicity)
ADH antagonists
Conivaptan, Tolvaptan
RAIU result in hCG secreting tumor
increased
Amiodarone effect on thyroid
hyper or hypo; decreased T4 to T3 conversion; low RAIU (saturated with iodine)
Most common cause of hypothyroidism
Chronic Autoimmune thyroiditis ("Hashimoto")
Causes of tongue enlargement
Hypothyoroid, Amyloid …
CBC finding in hypothyroidism
Normochromic normocytic anemia (except when associated with pernicious anemia)
Most common TSH/T4 in euthyroid sick
low tsh, normal t4 (should check this answer)
Biliary cirrhosis, hepatitis, clofibrate and narcotic effect on thyroid function tests
increase TBG
Meds that block t4 to t3 conversion
propranolol, glucocorticoids, propylthiouracil, amiodarone
Adrenal insufficiency affect on thyroid hormones
increased TSH
Test to differentiate secondary and tertiary hypothyroidism
sella imaging
medical comorbidity requiring slow titration of Thyroxine
CAD (especially elderly)
mortality of myxedema coma
30-40%
Two classic signs of myxedema coma
Decreased mentation and hypothermia
Eponym for automimmune adrenalitis and thyroiditis
Schmidt syndrome (suspect with hypoglycemia and hypothyroid)
Treatment for myxedema coma
passive rewarming, ivf, normalizing serum sodium, t3, intravenous t4 or both t3 and t4; stress dose steroids if any suspicion for adrenal insufficiency; empiric broad spectrum abx until infection excluded
Most common cause of thyrotoxicosis
Graves disease
Cause of abnormal ACTH stim test in hyperthyroidism
low cortisol binding protein; hyperthyroid patients usually don't have true adrenal dysfunction
buzzword for hyperthyroidism in the elderly
apathetic hyperthyroidism - "failure to thrive" picture
2 immune mediated hematologic abnormalities associated with Graves
pernicious anemia and ITP
Lab finding associated with reduced incidence of relapse of Graves after treatment
absence of stimulatory immunoglobulins
treatment of graves with history of prior radiation
surgery; give ptu or methimazole +/- beta blockers before surgery
Precipitating events (3) for thyroid storm
surgery, infections, iodine load
Treatment of thyroid storm (6)
1. IV propranolol or esmolol 2. high dose thionamide 3. iodine solution (blocks release of preformed hormone 4. iodinated contrast and glucocorticoids (blocks peripheral conversion) 5. empiric broad spectrum abx until infection excluded 6. supportive care in ICU (volume status, temperature, heart rate)
Cause of acute thyroiditis
Bacterial infection
Cause of subacute thyroiditis
Virus (also called granulomatous); PAIN - very tender neck, becomes fibrotic, returns to normal months later
Cause of chronic thyroiditis
autoimmune -mediated (Hashimoto's), painless, postpartum
TX of subacute (granulomatous) thyroiditis
ASA or NSAIDS; glucocorticoids in refractory (8 week taper); frequent reevaluation until thyroid fxn normalizes (1 week - most - to 12 months)
Percent of patients with painless thyroiditis that eventually develop Hashimoto's
50%
Eponym for thyroid tissue in an ovarian teratoma
Struma Ovarii
Percent of cold thyroid nodules that are benign
85%
nonmalignant thyroid nodule after neck radiation
colloid adenoma
Two diagnostic tests done after finding a palpable nodule
tsh and thyroid ultrasound; FNA if high low TSH and cold nodule, high TSH with concerning ultrasound, or normal TSH
Size criteria for FNA of incidentaloma (thyroid) with normal TSH
1 cm
principle cell involved with medullary thyroid cancer
parafollicular C cells
Gene involved in MEN2
RET protoncogene - tyrosine kinase, transduces signals for cell growth
Serum marker for medullary thyroid cancer
calcitonin
Spread of folllicular cancer is by what route and to what tissue
hematogenous; bone, lungs, CNS
spread of papillary cancer is by what route and to what tissue
lymphatics; bone, lungs
treatment of thyroid cancer
near-total thyroidectomy; posterior capsule often left in place to minimize the risk of recurrent laryngeal nerve damage; TSH allowed to rise to >30 then high dose radioactive iodine
follow-up studies for thyroid cancer in "remission"
neck ultrasound, total body scans, and/or thyroglobulin (interferred with by anti-TPO)
Concern when hashimoto's develops fast growing thyroid mass
Thyroid lymphoma
Vegetables that act as goitrogen
cassava root, Brussel sprouts, cauliflower, cabbage
3 main indications for treatment of nontoxic multinodular goiter
Compression of trachea, venous outflow obstruction, growth into intrathoracic area
Treatment of toxic multinodular goiter
usually ablative (I131)
3 zones of adrenal cortex
Zona Glomerulosa (salt), Zona Fasciculata (sugar - cortisol), Zona Reticularis (sex)
Product of chromaffin cells in adrenal medulla
mainly epinephrine
most common cause of CAH and resultant increased precursor
21 hydroxylase deficiency and 17 hydroxy progesterone
Enzyme deficient in late-onset CAH with hypertension and hyperkalemia
11 hydroxylase - causes increase in 11 deoxycortisol and 11 deoxycorticosterone (an active mineralocorticoid) in addition to testosterone
Cancers associated with ectopic ACTH
bronchogenic, pancreatic, thymic … carcinoid (if age > 60, then small cell lung cancer is the most common cause of Cushing's)
1st and 2nd most common cause of Cushing syndrome
exogenous steroids and pituitary adenoma (Cushing disease)
Causes of pseudo-cushing's
obesity, alcoholism, depression
What distinguishes Cushing disease and adrenal carcinomas from adrenal adenomas
Presence of increased androgens (adrenal DHEA) and hirsutism and acne
Failure of high dose dex to suppress cortisol production
Ectopic production of ACTH -> image with CT and check 5-hydroxyindoleacetic acid
Causes of Addison's disease
Autoimmune, granulomatous, HIV, CMV, amyloid, sarcoid
chronic mucocutaneous candidiasis, adrenal/pituitary insufficiencies +/- pernicious anemia, hepatitis, allopecia, Hashimoto's and premature ovarian failure
Polyglandular Autoimmune Syndrome I
>= 2 of the following Addison disease, hashimoto's, premature ovarian failure, type I diabetes +/- pernicious anemia, vitiligo, alopecia, sprue, myasthenia
Polyglandular Autoimmune Syndrome II
Most common cause of secondary AI
rapid withdrawal of chronic glucocorticoids
Primary adrenal insufficiency and hypothyroidism
Schmidt syndrome - give cortisol first; thyroid replacement first can worsen shock
Electrolyte that impacts aldosterone secretion
potassium
Most common cause of hypoaldosteronism
decreased production of renin in diabetic patients
Drugs that suppress aldosterone (directly or indirectly)
ACE inhibitors, NSAIDs, chronic heparin
Medications that interfere with work-up for primary and secondary hyperaldosteronism
ACEI/ARBs
Imaging test for pheo if CT/MRI normal
metaiodobenzylguanidine scintigraphy
Medication that interferes with urine metanephrines and catecholamines
TCA2 - wean two weeks prior to surgery, etc.
three familial cancer syndromes with pheos
MEN2, VHL, neuofibromatosis
new name for pheo outside the adrenals
extraadrenal paraganglioma
Pre-op med for pheo
Phenoxybenzamine then propranolol
incidentaloma not requiring a work-up
Myelolipoma
3 indications for removing adrenal incidentaloma
tests indicate a functioning tumor, mass is >6 cm, prior was <4 and evidence of growth on 6 month repeat
parathyroid hyperplasia, pituitary adenoma, pancreatic islet cell tumors (insulin, gastrin)
MEN1 (Wermer's)
(cardiac) myxomas, spotty pigmentation, and endocrine overactivity
Carney complex
Pheo, C cell hyperplasia -> medullary thyroid cancer, parathyroid hyperplasia
Men2a (sipple's)
Pheo, medullary thyroid, mucosal neuromas ("blubbery lips"), marfanoid body type
Men2b (or MEN III) - no consistent eponym
Diagnosis represented by "bilateral symmetric pseudofractures"; presenting symoms of bone pain and proximal muscle weakness
osteomalacia - commonly caused by vitamin d deficiency; usually caused by malabsorption
Test to diagnose osteomalacia
25(OH)D (not 1,25) - also marked by increased iPTH and alk phos, decreased Ca and decreased Phos
Effect of Magnesium on Calcium and MOA
Hypomagnesemia decreases PTH causing hypocalcemia
hypocalcemia with normal or elevated PTH and absence of 4th and 5th knuckles
pseudohypoparathyroidism - genetic mutation in PTH receptor
Drug of choice for myeloma-associated hypercalcemia
pamidronate
Guidelines for parathyroidectomy for Hyperparathyroidism (2008 guidelines)
Serum calcium 1.0 mg/dl above ULN, creatinine clearance < 60 ml/min, T-score < 2.5 at any site and/or previous fragility fracture, Age <50
Causes of hypercalcemia other than PTH (5+)
Vitamin D excess, Vitamin A excess, thiazide diuretics, lithium (increases PTH setpoint), benign familial hypocalciuric hypercalcemia, PTHrP, granulomatous diseases, bone mets, MM, immobilization *in setting of high turnover - thyroid, pagets, adolescence)
Mottled-looking band stretching horizontally across the center of the cornea
Band keratopathy in hypercalcemia
Subperiosteal bone resorption with a moth-eaten appearance to phalangeal cortex on finger radiographs
osteitis fibrosa cystica with prolonged PTH excess
Most common cause of vitamin d deficiency
malabsorption
Whipple's triad
hypoglycemic signs and symptoms, low glucose level, relief of symptoms with glucose administration
Two main categories of hypoglycemia symptoms
neuroglycopenic and autonomic
postrprandial hypoglycemia found in T2DM and in some post-GI surgical patients (when gastric contents get dumed into the small intestine too quickly with a brisk release of incretins)
Idiopathic reactive hypoglycemia
Four tests usined in the work-up of confirmed, nonreactive hypoglycemia
serum insulin, serum proinsulin (increased to >20% with insilunoma), c-peptide,urinary/plasma sulfonylurea test
Hormone that both increases osteoblasts (like corticosteroids) and inhibits osteoclasts (like calcitonin)
Estrogen
Autoantibodies in type 1 DM
anti-islet, -insulin, -glutamic acid decarboxylase, -tyrosine phosphatases IA-2 and IA-2beta
HLA (on chromosome 6) associated with DM
DR3 and DR4
Ketoacids in diabetes
Beta-hydroxybutyrate and acetoacetate (only one detected by Acetest)
Etiologies of brittle DM
gastroparesis, poor communication, malingering, increased growth hormone in puberty (increased insulin resistance)
Improvement of hyperglycemia after diagnosis and institution of treatment
Honeymoon effect
Increased blood glucose between 4 and 7 am with no preceding hypoglycemia
Dawn phenomenon (early morning rise in cortisol and GH)
Increased blood glucose with preceding hypoglycemia
Somogyi effect (classically at night with associate headaches and nightmares)
Triad of carbohydrate intolerance, glossitis, and erythematous rash
Glucagonoma
red, blistering rash that spreads across the skin, particularly the lower abdomen, buttocks, perineum, and groin
Necrolytic migratory erythema
analogue to amylin which is secreted by the pancreatic beta cells
Pramlintide - cut the insulin dose by 50% when using
sitagliptin moa
dipeptidyl peptidase 4 inhibitor
act by stimulating insulin release, inhibiting prostprandial glucagon release, slowing nutrient absorption, and accelerating satiety
byetta (glucagon-like peptide 1)
Nerves most often involved in diabetic mononeuropathy
CN 3 and 6, peroneal nerve (foot drop) and radial nerve (wrist drop)
glucose goals in pregnancy
60-90; <120 postprandial (note that pregnant patients require 50% more insulin)
Syndrome characterized by clinical and biochemical evidence of thyrotoxicosis, low 24-hour radioactive iodine uptake, nontender thyroid gland, and normal sedimentation rate
Silent (lymphocytic) thyroiditis or factitious (exogenous) thyrotoxicosis
Oral hypoglycemic agent that should discontinued prior to contrast imaging studies
metformin
Diagnosis suggested by high insulin, proinsulin, C-peptide levels and hypoglycemia
insulinoma
Long-acting, irreversible nonselective alpha-blocker used for pheochromocytoma
Phenoxybenzamine
Drug stimulates new bone formation by increasing osteoblast activity
Teriparatide (accept recombinant human parathyroid hormone)
This is a feared complication of removal of > 1 liter of fluid in a patient with a large pleural effusion
Reexpansion pulmonary edema
Light's criteria
protein ratio > 0.5, LDH ratio > 0.6, LDH fluid > 2/3 upper limit of normal
In a 24 y.o. pt with asthma and freq night symptoms, these 2 drugs are the mainstay of chronic therapy
Inhaled corticosteroids (#1) and long acting B agonists (#2)
Frequent asthma exacerbations, eosinophilia, elevated IgE and proximal bronchiectasis
Allergic Bronchopulmonary Aspergillosiss
Refractory asthma, pulmonary infiltrates, eosinophilia, and fever
Churg-Strauss Disease
Seen on CXR , this pleural based wedge shaped defect from infarction just above the diaphragm
Hamptom's Hump
Located near the hilum, this may be seen on CXR from a patient with confirmed PE
Westermark's sign
Extremely low values of this are seen in pleural effusions of patients with RA
Low glucose
Pleural effusion, LE edema, yellow nails
Yellow Nail Syndrome (2/2 disorder of lymphatics, pleural effusion can persist > 1 year); a history of bronchiectasis, bronchitis, or sinusitis in association with chronic pleural effusion should suggest the diagnosis.
Spirally twisted mucous plugs of shed epithelium that occur in the sputum of asthmatics
Curschmann's spirals
According to the ACCP, chest tube drainage is indicated in pleural effusions with a pH of this value
pH < 7.2; also glucose <60 or positive gram stain
Exudative criteria with better specificity than Light's
Serum-effusion albumin gradient LE 1.2; cholesterol effusion > 45 and LDHeff > 200
Markers for exudative effusion when concern for heart failure pseudoexudate
albumin gradient LE 1.2 and cholesterol >60
These 3 diseases are in the differential of an effusion with glucose <60
RA, malignancy, infection
Marker of chylothorax
Triglyceries > 110
The test used to distinguisha chylothorax with triglycerides from 50-110
Lipoprotein analysis to check for chylomicrons
Marker of urinothorax
Creatinine effusion/serum ratio GT 1
Aneurysmal dilation of a pulmonary artery that results from the local inflammation due to cavitary TB
Rasmussen's aneurysm
Mental status changes, petechiae (often in the axilla/thorax) and dyspnea
Bergman's triad (fat emboli syndrome)
Syndrome of pulmonary rheumatoid nodules in patient with co-existing coal worker's pneumoconiosis
Caplan's syndrome
Interstitial lung disease characterized by upper lobe masses in patient with known silicosis
Progressive massive fibrosis
Slowly progressive pulmonary syndrome associated with cystic changes in the lungs occurring almost exclusively in smokers
Pulmonary Langerhans Cell Histiocytosis
The earliest pleural manifestation of asbestos exposure
benign asbestos pleural effusion
Neck circumference measurement associated with an increased risk of obstructive sleep apnea
> 17 inches (43 cm)
Disease with chest CT findings described as "crazy paving"
Pulmonary alveolar proteinosis
Shortness of breath in the erect position
Platypnea
Laryngeal finding associated with vocal cord dysfunction
Adduction of vocal cords (or paradoxical motion of vocal cords)
Inhaled drug that is effective for bronchoconstriction due to propranolol
Ipratropium
Cystic lung disease in women of childbearing age
Lymphangioleiomyomatosis
Late, severe complication of silo filler's disease
Brochiolitis obliterans
Upper airway complication of prolonged intubation
Tracheal stenosis (or tracheomalacia)
Syndrome characterized by quadriplegia, paralysis of horizontal eye movements with preservation of vertical eye movements, and inability to speak
Locked in syndrome
Smoke inhalation victim with coma, hypotension, profound anion-gap metabolic acidosis unresponsive to volume replacement and oxygen
Cyanide poisoning
Three things that move oxyhemoglobin curve to the right
decreased pH, increased temp, increased 2,3 DPG (diphosphoglycerate)
Wool Sorter's disease (causative organism)
Bacillus anthracis
Continuous LTOT would be indicated with a pO2 56-59 in these patients
Those with resting pO2 56-59 with edema, cor pulmonale, or Hct>56
Interventions that increase oxygenation in an intubated patient
increased FiO2, increased PEEP, increased I/E ratio
cyclic crescendo-decrescendo respiratory effort and airflow during wakefulness or sleep (associated with heart failure)
Cheyne-Stokes
Fat Emboli Syndrome
Bergman's Triad - petechia, dyspnea, MS changes
Besides ABCs and aggressive fluid resuscitation, these are 4 additional treatment options in CCB overdose patients
IV calcium, IV glucagon, IV insulin and glucose (high dose 1u/kg insulin bolus), cardiopulmonary bypass? (May also accept pressors, pacemaker, atropine, phosphodiesterase inhibitors, aortic balloon pump, activated charcoal)
Description of mediastinum LN in sarcoid
Potato nodes
Patient with SLE admitted for SOB. DLCO elevated. DX?
Diffuse Alveolar hemorrhage
Feared complication from too rapidly correctin a patients significant hypernatremia
Cerebral edema
Hemoptysis and tram-tracking on CXR
Bronchiectasis
Components of Samter's triad
ASA sensitivity, nasal polyps, asthma
Histologic findings in Hamman-rich syndrome
Organizing diffuse alveolar damage
Mode of mechanical ventilation wher there is a set tidal volume and rate and the patient gets the set tidal volume with every breath
AC
The TV in ARDS patients should not exceed this
6 ml/kg of predicted weight
Acute sarcoid with anterior uveitis, parotid enlargement, fever, and facial nerve palsy
Heerfordt Waldenstrom Syndrome
Suspect his as a cause if patient's hypoxia does not correct with 100% FiO2
Shunt
5 general causes of hypoxemia
Decreased FiO2, hypoventilation, shunt, VQ mismatch, decreased diffusion
Causes of increased DLCO
asthma, L to R cardiac shunting, diffuse alveolar hemorrhage, polycythemia, obesity
Over 90% of massive hemoptysis comes from these arteries
Bronchial arteries
Dyspnea occuring only in upright position
Platypnea (associated with hepatopulmonary syndrome)
Desaturation in the upright position but better in the supine position
Orthodeoxia (associated with hepatopulmonary syndrome)
Oxygen saturation gap is associated with this
methemoglobinemia (cyanosis with a normal PaO2)
Congenital central hypoventilation syndrome associated with this GI disease
Hirschprung's disease (also associated with neuroblastoma and dysphagia)
Congenital disease with decreased autonomic control of ventilation, central sleep apnea (eponym)
Ondine's curse
2 causes of heme-negative hemoptysis
Serratia marcecens, INH treatment
Microscopic findings in Langerhans Cell Histiocytosis
Staining for S100 and CD1a or anti-langerin. Also birbeck granules may be seen
Spontaneous pneumothorax now with chylous effusion
Lymphangioleiomyomatosis
Lymphangioleiomatosis can be associated with a higher incidence of this neuro malignancy
Meningioma
Treatment for LAM
Hormonal manipulation but of unproven benefit; also sirolimus or lung transplantation (Oophorectomy not recommended, progestin, tamoxifen, GnRH analogs)
Cartilage disorder and bronchiectasis (eponym)
william Campbell
eponym for hyperpigmented patches on thighs proximal to the knees, from chronic elbow pressure as the emphysematous patient rests leaning forward to improve breathing
Dahl's sign
The age at which medicare takes effect
65
This part of Medicare pays for physician office visits, ambulanc rides, and outpatient treatments administered in a doctor's office
Part B
This part of Medicare covers inpatient treatment
Part A
Medicare Advantage plans (privatized)
Part C
Prescription Drug Plan
Part D
BMI values
Obesity if >30, Overweight if 25-30
Metabolic syndrome
three or more of the following: 1. Blood pressure equal to or higher than 130/85 mmHg 2. Blood sugar (glucose) equal to or higher than 100 mg/dL 3. Large waist circumference (length around the waist): Men - 102 cm or more Women - 88 cm or more 4. Low HDL cholesterol: Men - under 40 mg/dL Women - under 50 mg/dL 5. Triglycerides equal to or higher than 150 mg/dL
President W. Henry Harrison
Pneumonia
President Kennedy's tan
Addison's disease
President George Washington
epiglottitis
President Andrew Jackson
Heart Failure
Risk factors for developing preeclampsia
1. Nulliparity 2. Chronic HTN 3. family history 4. renal disease 5. diabetes 6. obesity
Name applied to decision making for a patient whose preferences are not known but are based upon the best evidence of what the patient would have wanted
Substituted Judgement
Federal law requiring health care institutions participating in Medicare/Medicaid to ask if a patient has an advance directive, to provide information about advance directives, and incorporate advance directives into the medical record
Patient Self-Determination Act of 1990
In 50% of women with contraceptive associated hypertension, the blood pressure will return to normal within this time span
3 months
Diagnosis suggested by dyspareunia and punctate ulcers in the vestibule located primarily around the Bartholin's glands
Vulvar vestibulitis
Pregnancy complication of untreated Trichomonas vaginitis
PROM or preterm delivery
Federal Act of 1996 contains rules about privacy of medical records
Health Insurance Portability and Accountability Act (HIPAA)
An advance directive appointing a surrogate who will make decisions if the patient is unable to do so
Durable power of attorney (for health care)
Name describing generalized swelling of an entire digit
Dactylitis
Eponym for a bruise over the mastoid, indicating a basal skull fracture
Battle's sign
Chronic renal failure increases risk for this third trimester pregnancy complication
Preeclampsia
Vasodilator of choice for peripartum cardiomyopathy
Hydralazine
Treatment of gestational hypertension improves this renal outcome
Decreased proteinuria
Probability of a positive test in a patient with disease compared to the probability in a patient without disease
Positive likelihood ratio
Breast cancer prediction model based upon personal and family risk factors
Gail model
Best trimester to perform "semi-elective" abdominal surgery
2nd trimester
Normal PCO2 level during pregnancy
28-32 mm Hg (accept any answer within range)
Major fetal effect of maternal ACE inhibitor use
Renal tubular dysgenesis
In pregnant patients with a normal fasting glucose, what screening test at 24-28 weeks is recommended for the detection of gestational diabetes
What is 50-g glucose tolerance test at 24-28 weeks gestation?
Therapy indicated in a 28 yo gravid female at 10 weeks with a low TSH and normal T4 that was found on routine testing
What is no therapy is necessary? HCG during the 1st trimester is in high concentration and acts as a partial TSH agonist. Recheck later in pregnancy.
Diagnostic criteria for preeclampsia
What is systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg (on two separate occasions with prior normal BP after 20 weeks gestation) and proteinuria of 300mg or greater in a 24-hour urine specimen?
Ingredients in lactated ringer
chloride, potassium ,calcium, lactate, sodium,water
5 As for quitting smoking
Ask, Advise, Assess, Assist, Arrange
Deficiency of this vitamin results in cardiomyopathy and muscle pain
Selenium
Most likely deficiency in person with anemia, cheilosis, and seborrheic dermatitis who takes a tricyclic antidepressant
Riboflavin (Vitamin B2)
Most common cause of jaundice during 1st and 2nd trimesters
Acute viral hepatitis
Stunted growth, loss of adipose tissue, generalized wasting of protein mass, no edema
Marasmus (protein and energy deficiency)
Growth failure, edema, hypoalbuminemia, fatty liver, preservation of subcutatneous fat
Kwashiorkor (protein deficiency
Dermatitis, dementia, diarrhea
Pellagra (niacin deficiency)
High output heart failure, peripheral neuropathy, Wernicke's encephalopathy, Korsakoff syndrome
Beriberi (thiamine deficiency)
Perifollicular hyperkeratotic papules, purpura, poor wound healing, hemorrhages
Scurvy (vitamin C deficiency)
Location of surgeries associated with greatest risk in patients with COPD
Upper abdominal or thoracic
Duration of prophylactic antibiotics for uncomplicated surgical procedures
24 hours
Recommended preoperative screening prior to cataract surgery
None
Percentage of patients with a negative history but abnormal bleeding tests that require preoperative treatment
0.3% (Less than 1% acceptable)
General surgery may be safely performed if the INR is below this level
1.5
Vitamin deficiency noted bby dwarfism, gonadal atrophy, severe dermatitis, alopecia
Zinc
Vitamin deficiency noted by cardiomyopathy, proximal muscle weakness, macrocytosis, pseudoalbinism
Selenium (Keshan disease)
Enzyme deficiency in Tay-sachs
hexosiminadase A
Enzyme deficiency in Niemann Pick
Sphingomyelinase
5 Kubler-Ross stages of grief
Denial, Anger, Bargaining, Depression, Acceptance
Name all of the clinical competencies
1. Medical Knowledge,2. Professionalism, 3. Practice Based Learning and Improvement, 4. Systems based learning/practice, 5. Interpersonal/communication skills, 6. patient care
Formula for relative risk
RR = pexposed/pnotexposed = [a/(a+b)]/[c/(c+d)]; used in cohort and randomized/prospective studies
Formula for odds ratio
ad/bc (used in case control and retrospective studies)
Marfanoid habitus, increased risk of strokes, and CAD is seen in this congenital syndrome
Homocysteinuria syndrome
2008 Guidelines for surgery for asymptomatic hyperpara
Age < 50, Creatinine > 1mg/dl over ULN, creatinine clearance < 60 ml/min, T score < 2.5
He was a US Army chemist and surgeon credited with originating the technique of liquid chlorination of drinking water. It has been plausibly asserted that more lives have been saved and more disease prevented by this contribution to sanitation than by any other single achievement in medicine or public health.
Dr. Carl Rogers Darnall
Nobel awardee for development of electrocardiogram
Willem Einthoven
First to provide experimental proof that blood was pumped through a closed circulatory system
William Harvey
The 1910 report that revolutionized medical education and established current system of education
Flexner report
First to use mecury in a thermometer to measure temperature
Gabriel Daneil Fahrenheit
Persian physician who gave first accurate description of measles and smallpox
Rhazes (Razi)
first to describe angina pectoris
heberden
Invented blood storage and the first blood bank; started Red closs blook bank; mobile blood stations in WWII
Charles Drew
Highest DO rank, commander WRAMC
LTG Ronald Blanck
1st true surgeon general, weather records, started library
Joseph Lovell
The first surgeon general of the air force; achievements included developing body armor to protect combat crews; devloping electrically heated clothing, device to protect gunners from windblast, etc.
Malcolm Grow
assistant army surgeon during the Apache wars who was the first Medal of Honor award winner (chronologically by date of action)
Bernard Irwin
American neurologist and surgeon general who founded the Army Medical museum and co-founded the American neurological Associatoin
William Hammond
Typhoid vaccine
MAJ Frederick Russell
first meningitis polysaccharide vaccine
MAJ Ronald Gold
Army nurse corps chief, 1st female general in Army history
Anna Hays
Promoted immediately after Anna Hays, the 2nd female general in Army history
Hoisington
This former Walter Reed and Tripler-based Army physician is credited with recognizing the entity of agammaglobulinemia most often seen in young boys
Ogden Bruton
Under the guidance of this former Army surgeon general, Army hospitals became training institutions for the first time in history by offering residency training programs to the career officer
Raymond Bliss
Preferred treatment for acute episodes of angioedema in hereditary angioedema
C1-INH (inhibitor) concentrate (accept danazol or stanzolol)
Complement level that typically remains low between attacks of hereditary angioedema
C4
3 rare but severe side effects of IVIG administration
anaphylaxis, volume overload, renal failure, aseptic meningitis
Patients with this immune deficiency should not receive IVIG
IgA deficiency
The MMR vaccine contains a small amount of this antibiotic
Neomycin (avoid MMR if patient is allergic to neomycin
Low IgM, high IgA and IgE
Wiskot-aldrich syndrome
Patient becomes pregnant despite daily OCPs
antibiotics, phentyoin, rifampin
Patient with elevated LDL and triglycerides develops rhabdomyolysis while taking simvastatin
Gemfibrozil
Patient with well treated hyperlipdemia, a-fib, and hypertension develops rhabdo while taking Zocor
Diltiazem or verapamil (Ca channel blocker)
Patient with GERD and anemia fails treaatment with Levaquin for their CAP
antacids, iron or Zn
Hypothyroid patient with heavy menses remains hypothyroid despite escalating her synthroid dose
iron, calcium
Aspirin MOA
irreversible cyclooxygenase inhibitor (platelets)
Plavix MOA
Inhibits binding of ADP to platelets
Integrillin (eptifibitide) MOA
blocks the GP Iia/IIIb platelet receptor
Heparin MOA
Antibthrombin III activator
This chemotherapy can cause auditory toxicity
Cisplatin
This chemotherapy can cause HUS
Mitomycin C
This cancer treatment can cause an ARDS like presentation
All trans retinoic acid
Lipid lowering agent that is least likely to interact with antiretrovirals
Pravastatin

This antiepileptic is structurally similar to TCAs

Carbemazipine
Risk of giving pentamidine IV
Torsades des pointes
Dose limiting toxicity of vincristine
peripheral neuropathy
Treatment of TB with this medicine may aggravate gouty symptoms
Pyrazinamide
Estrogen found in most OCPs
Ethinyl estradiol
Androgen used in hereditary angioedema
Danazol
Overdose of this causes CNS depression, tachycardia, QT prolongation
TCA
AIDs medication that can cause bluish discoloration of the nails
AZT
Herbal antidote to deathcap mushrooms
Milk thistle
Nmbing sensation on tongue when taken orally
Echinacea
High doses can decrease blood levels of some anti-convulsants
Ginko biloba
Can cause premature contractions
Black cohosh
used for migraine treatment
Feverfew
Treatment for eczema or arthritis
Evening primrose
Urology medicine associated with pulmonary fibrosis
Nitrofurantoin
Gardasil
6/16/2018
indications for AoVR
1.) symptomatic AS, 2.) asx severe with LVEF <50%, 3.) asx severe with AoVA <0.6, gradient >60, jet >5 m/s or high likelihood of rapid progression, 4.) also c/w patients in mod-sev asx AoS undergoing CABG, valvular or Ao root surgery
natural progression for AS
"ASK (actually ASC) 532", angina 5yr mean survival, syncope 3yr mean survival, CHF 2 yr mean survival; typically 0.1cm per yr decrease in AoVA; follow with TTE q1-2y in mod, q3-5y in mild
medical Rx for AoS
HTN control, caution with diuresis, maintenance of NSR, statin, avoiding venodilators and negative ionotropes in more severe disease
hematologic abn a/w more severe AS
acquired von Willebrand disease (destruction of vWF by shear forces)
Class I recommendation for GXT
1. intermediate pretest probability of CHD 2. prognosis and managment of patients with prior CHD including stable angina or prior MI 3. Screen for CHD in high risk asymptomatic populations (not routine screening for DM or CKD) 4. Eval exercise capacity and response to therapy in heart transplant list patients 5. Assist in differentiation between cardiac and pulmonayry causes of dyspnea 6. Identify appropriate settings in patients with rate adaptive pacemakers 7. Eval patients with congenital complete heart block prior to sports/increased activity
Contraindications to GXT
1. Acute MI within last 2 days 2. Unstable angina 3. Uncontrolled arrhythmias causing symptoms/hemodynamic 4. Symptomatic severe AS 5. Uncontrolled symptomatic HF 6. Active endocarditis/myocarditis/pericarditis 7. Acute aortic dissection 8. Acute embolism 9. Acute noncardiac disorders that may affect exercise 10. Baseline ECG abnormalities including preexcitation, complete LBBB, more than 1 mm ST depression at rest, paced ventricular rhythm, use of digoxin
Positive exercise stress test
60 to 80 ms of 1mm or greater horizontal or downsloping ST depression or elevation (lead V5 most diagnostic) Others: 1. Poor exercise capacity (< 5 Mets) 2. exercise induced angina 3. Low peak systolic blood pressure (<130) or fall in blood pressure 4. Chonotropic incompetence 5. New S3
Absolute Fibronylitic Contraindications
1. any prior intracranial hemorrhage known structural cerebral vascular lesion (AVM) 2. Known malignant intracranial neoplasm Ischemic stroke within 3 months (except if within 3 hours) 4. Suspected aortic dissection 5. Active bleeding or bleeding diathesis (not menses) 6. Significant closed head trauma or facial trauma within 3 months
Relative Fibrinolytic Contraindications
1. History of chronic, severe, poorly controlled HTN 2. Severe uncontrolled HTN on presentation (SBP > 180 or DBP > 110) 3. History of prior ischemic stroke > 3 months, dementia or known intracranial pathology 4. Traumatic or prolonged (>10 mintes) CPR or major surgery (<3weeks) 5. Recent (within 2-4 weeks) internal bleeding 6. Noncompressible vascular punctures 7. Pregnancy 8. Active peptic ulcer 9. Current use of anticoagulant (worse the higher the INR) For streptokinase/anistreplase: prior exposure (>5 days ago) or prior allergic rx to these agents

a

a

Venous waveform letters
a = atrial contraction c = closure of TV with early ventricular contraction - bulging of TV back into RA x = atrial relaxation, downard movement of ventricle during contraction v = venous filling against a closed valve y = opening of TV
Cardiac output
Q=SVxHR
O2 extraction ratio-
SaO2-SvO2/SaO2
O2 delivery-
Q x CaO2
FICKS equation for oxygen consumption
VO2 = Q(Ca -Cv) (volume of oxygen used = cardiac output (difference in oxygen content)
Oxygen content
(1.34 x HB x SaO2) + (0.0031 x PaO2)
Causes of Complete Heart Block
Medication Ischemia CNS - Cushing's reflex (increased intracranial pressure) Metabolic - Hyperkalemia (usually greater than 6.3) Hypo/hyperthyroid Infection - Lyme Rheum - SLE, dermatomyositis Sarcoid High Vagal tone Lenegre-Lev syndrome
The ejection fraction or systolic left ventricle internal diameter used as in indication for surgical intervention in severe mitral regurgitation
Left ventricular ejection fraction < 60% or left ventricular internal diameter in systole > 45 mm
amiodarone toxicity
1. CARDIAC: hypotension with rapid infusion, prolonged QT, torsades 2. NEUROLOGIC problems occur in 20-40%, including malaise, ataxia, and peripheral neuropathies 3. ENDOCRINE: hypothyroidism and hyperthyroidism 4. GI problems occur in 25% 5. OPHTHALMOLOGIC disturbances include optic neuropathy, papilledema, and photosensitivity 6. SKIN: blue grey pigmentation 7. PULMONARY: pulmonary fibrosis
Indications for IE prophylaxis
1. Previous IE 2. Prosthetic heart valve 3. Unrepaired cyanotic heart disease (including palliative shunts and conduits); 4. Completely repaired congenital heart defects with prosthetic material or device, whether placed by surgery or by percutaneous catheter intervention, during the six months after the procedure; 5. Repaired congenital heart disease with residual defects at the site, or adjacent to the site, of a prosthetic patch or prosthetic device (which inhibit endothelialization); and 6. Previous cardiac transplantation with subsequent cardiac valvulopathy (substantial leaflet pathology and regurgitation).
HPV strongly associated with cervical cancer
16, 18, 31, 45
Vector for ehrlichiosis
HME - Ambyomma americanum, dermacentor variabilis HGA - Ixodes
Organism for spotless RMSF
Erhlichiosis chaffeensis - human monocytic erlichiosis Also: Anaplasma phagocytophilum - Human granulocytic anaplasmosis