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218 Cards in this Set

  • Front
  • Back
Banana Bag
Thiamine 100 mg
Folic acid 1 mg
MVI 1 amp (Multivitamin for infusion, 1 ampule)
3 grams of magnesium sulfate
Wernicke's encephalopathy
1. Ocular disturbances (nystagmus)
2. Changes in mental state (ataxia)
3. Unsteady stance and gait
Korsakoff's syndrome
1. Anterograde amnesia
2. Variable presentation of retrograde amnesia
Wernicke–Korsakoff Syndrome
Severe thiamine deficiency
Atropthy/Infarction of mamillay bodies

DO NOT give glucose without giving thiamine as glucose will exhaust any current thiamine in system and exacerbate WKS
Aphasia
Disturbance of the comprehension and formulation of language
Apraxia
Disturbance of the comprehension and formulation of language
Risk of preoxygenation
Gives you THREE minutes where your O2 sats will not drop. You don't want to wait to intervene.....LOOK AT END TIDAL CO2 INSTEAD
What to do for obstruction in the office
1. Suction
2. Jaw thrust/chin lift
3. Tongue Pull
4. Oral/Nasal Airway
5. Positive Pressure Ventilation
6. 100% Oxygen
Diff Dx of Obstruction
1.Laryngospasm - sux 0.2mg/kg (20mg)
2.Aspiration
3.Asthma- Epi 0.2mg (2cc 1:10,000)
4. Allergic rxn- Benadryl 50mg, epi 0.2mg, decadron 8mg
5. Bronchospasm- Prop 50mg, Ketamine 50mg, Epi 0.2mg
5 Differences between Pediatric and Adult Airway
1. Larger tongue
2. Higher (C 1-2 vs C 4-5) and more anterior airway
3. Floppy Trachea
4. Narrowest part is cricoid vs vocal cords in adults
Stage 1 Anesthesia
"induction", the period between initial administration of induction agents and loss of consciousness. During this stage, the patient progresses from analgesia without amnesia to analgesia with amnesia. Patients can carry on a conversation at this time.
5 Differences between Pediatric and Adult Airway
"excitement stage", is the period following loss of consciousness and marked by excited and delirious activity. During this stage, respirations and heart rate may become irregular. In addition, there may be uncontrolled movements, vomiting, breath holding, and pupillary dilation. Since the combination of spastic movements, vomiting, and irregular respirations may lead to airway compromise, rapidly acting drugs are used to minimize time in this stage and reach stage 3 as fast as possible
Stage 3 Anesthesia
"surgical anaesthesia". During this stage, the skeletal muscles relax, vomiting stops , and respiratory depression occurs . Eye movements slow, then stop, the patient is unconscious and ready for surgery. It has been divided into 4 planes:

1. eyes initially rolling, then becoming fixed
2. loss of corneal and laryngeal reflexes
3. pupils dilate and loss of light reflex
4. intercostal paralysis, shallow abdominal respiration
Stage 4 Anesthesia
"overdose", is the stage where too much medication has been given relative to the amount of surgical stimulation and the patient has severe brain stem or medullary depression. This results in a cessation of respiration and potential cardiovascular collapse. This stage is lethal without cardiovascular and respiratory support.
Rational for ACLS protocol
1.SHOCK- give a new start
2. EPI- Large sympathetic and vasoconstrictive push to help the shock
3. Amiodarone- Treat a possible arrhythmia if 1 and 2 are not working
H's of ACLS
Hypovolemia
Hypoxia
Hydrogen ion – acidosis
Hyperkalemia / Hypokalemia
Hypothermia
Hypoglycemia and other metabolic disorders
T's of ACLS
Tablets (drug OD, accidents)
Tamponade (cardiac)
Tension pneumothorax
Thrombosis, coronary (ACS)
Thrombosis, pulmonary (embolism)
Trauma
CIWA Components
Nausea / vomiting
Anxiety
Paroxysmal sweats
Tactile disturbances (itching, bugs crawling on skin)
Visual disturbances
Tremors
Agitation
Orientation
Auditory disturbances
Headache
Psychiatric symptoms of ETOH withdrawal
disorientation, confusion,
agitation, anxiety, restlessness, visual/audio hallucinations,
paranoia, amnesia, anger, insomnia, coma.
Sympathetic symptoms of ETOH withdrawal
tachycardia, hypertension,
sweating
Physical Symptoms of ETOH withdrawal
tremors, fever, sweating
Delerium Tremens
Delirium
severe autonomic hypersensitivity
Formication
global confusion
constant tremor
fumbling movements of the hands
insomnia
Submental Triangle Boundries
disorientation, confusion,
agitation, anxiety, restlessness, visual/audio hallucinations,
paranoia, amnesia, anger, insomnia, coma.
Submandibular Triangle Boundries
Ant and post bellies of digastric and inferior border of mandible
Buccinator Nodes
Part of perifacial nodes. Can be positive when primary site of disease is lip, buccal mucosa, anterior nasal cavity, and soft tissue of the cheeck
Level II of the neck
contains upper jugular and jugulodigastric nodes and also the SPINAL ACCESSORY

IIa is anterior to SA
IIb is posterior to SA

skull base to carotid bifurcation (hyoid)
Level III of the neck
contains middle jugular lymph node group including juguloomohyoid nodes.

from hydoid/carotid bifurcation to cricothyroid/junction of omohyoid with jugular
Level IV of the neck
contains the lower jugular lymph node group.

from cricothyroid/omohydoid jug junction to clavicle
Submandibular Triangle Boundries
parathryoidal, paratracheal, precricoid (delphian)

positive in thryoid, piriform sinus, subglotic, cericval esoph and cervical tracheal disease.
Modified radical neck
Preservation of any of the three stuctures

I. Spinal Accessory
II. + Jugular
III. ++ SCM
Selective neck
Sparing of one or more LYMPH NODE GROUPS that would usually be taken in RND
Types of Selective Neck Dissections
SOH
Lateral
Posterolateral
Anterior Compartment
FOM and Tongue cancer spreads to which nodes?
Submental, submandibular, upper and middle jugular nodes
Contra lateral theraputic neck dissection should be done when....
N2C disease (contralateral node 3-6cm in size)
Selective neck dissection- lateral type
En bloc resection of II, III, and IV

indicated in ca of oro, hypo and larynx
Selective neck dissection- Posterolateral Type
En bloc resection of II to V and suboccipital and postauricular nodes

used for posterior scalp, nuchal ridge, occiput or posterior upper neck malignancies

nodes include post auricular nodes, occipital, posterior triangle and jugular groups
Selective neck dissection- Anterior Type
En bloc removal level VI nodes

thyroid, hypo, cervical trachea, cervical esoph, larynx

removal of perithyroidal, pretracheal, paratracheal, delphian
CT criteria for cervical metastasis
1. any node larger than 1.5cm
2 .central lucency of node
3. irregular borders
4. loss of plane between mass and adjacent structure
Stage I Ca
T1, N0, M0
Stage II Ca
T2, N0, M0
Stage III Ca
T3, N0, M0
T1,2,3 with N1 ,M0
Stage IV Ca
T4 ,N0 or N1, M0

Any T, if with N2 or 3
Any T, if with M1
Triple Scope
Laryngoscopy
Bronchonsopy
Esophogoscopy
Inications for RND
1. One or more clinically positive nodes are present
2. Nodal involvement other than first echelon
3. High risk of occult positive nodes
4. Regional mets after primary has been treated
5. positive node after previous radiation
6. fixed neck mass that becomes mobile after radiation
CONTRAINDICATIONS to RND
1. uncontrollable cancer
2. distant mets
3. nodes unchanged by radiotherapy
4. short life expectancy (less than 3 months)
CT criteria for cervical metastasis
1. Electively when there is >20% chance of occult disease and surgery if being done for primary
2. ipsilateral when it is to be followed by radiotherapy
Basic Radiation Therapy
2 y per day for 5 to 7 weeks for a total of 55-65 grays

external beam radiation
Reasons for radiation alone
Small cancers
Poor surgical access
functional disability that will be less with rad- swallowing, speech
Side effects of radiation
Mucositis
Xerostomia
ORN
Reasons for postop radiation tx
1. advance primary disease- t3 or 4
2. close positive margins
3. multiple positive neck nodes
4. extracapsular extension
Why post op rather that pre op radiation??
1. to avoid a difficult dissection
2. to avoid loss of well defined margins
3. would healing complications
4. can deliver a higher dose post than preop

but one big problem is that would complications delay post op rad which should ideally be given within 6 weeks
Upper lip and commisure ca spread to?
preauricular, periparotid, submandibular nodes
Lower lip ca spreads to?
Submental and submandibular nodes
Initial reaction to vessel injury
1. Vasoconstriction
2. Release of
1. vWf
2. Collagen
3. Tissue Factor (III)
Most powerful platelet activators
Collagen
Thrombin
Platelet granules
Dense Granules- secrete serotonin, ADP, ATP, Calcium

Alpha Granunes- secrete vWF, fibringogen (I), V and XI, protein S
PLatelet pathology
2 y per day for 5 to 7 weeks for a total of 55-65 grays

external beam radiation
Extrinsin Pathway
III activates VII then activiates extrinsic pathway (X to II to I)
Intrinsic (Propogator) Pathway
XII, XI, IX, (VIII), X to Xa
Common Pathway
Xa turns II into IIa (thrombin) which turns I (fibrinogen) into Ia (fibrin)
Antiplatelet vs Anticoagulant
Anticoagulant blocks FIBRIN formation
CHADS2
C - CHF 1
H - HTN 1
A - AGE >75 1
D - DIABETES 1
S - STROKE 2

Used to stratify stroke risk
0 is 1.9% stroke risk
6 is 18.2% stroke risk
Upper lip and commisure ca spread to?
Bare metal
Drug Eluting


In first year drug eluting stents have higher risk of thrombosis as oppoed to BMS which is 1 month
IIb/IIIa inhibitors
Abciximab
Eptifibitide
Tirofiban

ONLY IV- Used in AMI and PCI
ADP Inhibitors
plavix, prasugrel, tigacrelor, ticlodipine
NSAID MOA
blocks cox from converting arachodonate to PG A2 which then forms TA2 which causes vasoconstriction and PLATELET AGGREGATION
COX 1
Increases

Mucosal integrity
Platelet aggregation
Vasoconstriction
Vascular porliferation
COX 2
Platelet aggregation
Vasoconstriction
Vascular porliferation
Plavix vs prasugrel
Both are prodrugs that need to activated. Plavix activated by CYP450 2C19 (liver). Prasugrel does not need this to be activated

Approximately 30% of population is missing this enzyme

BUT prasugrel does have higher risk of serious bleed

Both are IRREVERSIBLE
Ticagrelor
does not require liver biotransformation like plavix and prasugrel

REVERSIBLE
Stents and surgery
DES- Wait 6 months

BMS- Wait 6 weeks

DO NOT TAKE OFF DUAL ANTIPLATELET THERAPY
Natural Anticoagulants
AT III
Tissue Factor Pathway Inhibitor (TFPI)
Protein C/S
Vitamin K dependent co-factors
2,7,9,10 and protein c/s
INR and odds ration of stroke
Anticoagulant blocks FIBRIN formation
LMWH
inactivates Xa

thrombin (IIa) is partially inactivated

can be reversed with protamine

Less frequent dosing
No need for APTT
Less risk of HIT
Factor Xa inhibitors
Fondapurinox (Arixtra) - subq

Rivoroxaban (Xarelto)- Oral
Antofibrinolytics
Amicar- Aminocaproic acid
Tranexamic acid

Inhibit conversion of plasminogen to plasmin..therefore increase clot stabilization
Direct Thrombin Inhibitors
Hirudin
Argatroban

Dabigatran (Pradaxa)- Oral

NO REVERSAL AGENTS
Brain Volume with growth
Triples in first year
Quadruples by second year
NSAID MOA
14% with one fused suture
42% with more than one fused suture
Trigonocephaly
Meitopic suture synostoses
Midline forhead ridge
Triangular shape
Hypotelorism
Bitemporal narrowing
Scaphocephaly
Saggital suture synostosis
Biparietal and bitemporal narrowing
occipital protuberence
varrying degree of frontal bossing
Anterior Plagiocephaly
Unilateral coronal suture synostosis
oblique/flat shape
unilateral palpebral fissure widening
unilateral supraorbital rim displacement sup and post
Elevation of ear, sphenoid wing (harlequin)
Flattning of root of nose on affected side
Brachycephaly
Bilateral coronal suture synostosis
"short head"
apert, crouzon, pfeiffer
bilateral palpebral fissure widening
bilateral supraorbital rim displacement sup and post
bilateral harlequin
Posterior Plagiocephaly
Lambdoid suture synostosis
Components of epidermis
Keratinocytes - structural integrity
Langerhan- Immune response
Melanocytes- Pigmentation
Merkel Cells- tactile receptors
3 phases of wound healing
Inflammatory
Proliferative
Remodeling
Accutane
Isoretinoin- kills sebaceous glands so acne can't form
Types of peels
Keratolytic - aha (glycolic acid), salicylic acid
Disprupt keratinocyte adhesion and promose collagen production

Protein denaturants- TCA, Obagi blue, phenosis
Cause protein coagulation and denaturation

Retin A- compacts stratum corneum, increases cell turnover and increases collagen production
Problem with deep peels
Phenols and bakers or littons solutions

ARRHYTHMOGENIC
Papillary
inactivates Xa

thrombin (IIa) is partially inactivated

can be reversed with protamine

Less frequent dosing
No need for APTT
Less risk of HIT
Acanthotic
Thick
Layers of epithelium
Basal
Spinous
Granular
Keratin
Desmoplastic/fibrotic/sclerotic/hyalinized
pink, dense, few nuclei
ectatic
dilated (vessels or ducts)
Plasmacytoid
nucleus is pushed off to one end
Craniosynostoses and increased ICP
wide variety
cherry red nuleolus
Melanoma
parakeratin
nuclei are present
orthokeratin
no nuclei
bigger granular cell layer
2 types of salivary gland cells
acinar
serous
spindle shaped nucleus
elongated- think nerve tissue
saw tooth rete ridges
think lichenoid
peripheral palisading
reverse polarity
ameloblastoma
hpv driven scca occurs where
oropharynx vs oral cavity
with central giant cell granuloma, you need to rule out what?
rule out hyperparathyroidism (brown tumor)- get PTH level
central giant cell granuloma non surgical treatment
intralesional steroids
intranasal calcitonin
secondary hyperparathyroidism caused by
Keratolytic - aha (glycolic acid), salicylic acid
Disprupt keratinocyte adhesion and promose collagen production

Protein denaturants- TCA, Obagi blue, phenosis
Cause protein coagulation and denaturation

Retin A- compacts stratum corneum, increases cell turnover and increases collagen production
Absorbable sutures
Gut
Vicryl
Monocryl
PDS
Absolute Indications for opening a condyle
1. Displacement of condyle into middle cranial fossa
2. Inability to obtain adequate occlusion with MMF
3. lateral extracapsular displacement with esthetic deformity
4. foreign body in joint space
Relative Indications for opening a condyle
1. bilateral
2. uni or bi where MMF would not be tolerated
3. bilateral condylar fx with unstable midface fx's where vertical butresses cannot be reconstructed
4. bilateral fxs with gnathological problems such as apertognathia, prognathism, retrognathism or dental abnormalities (perio dx, loss of teeth)
5 Differences between peds and adult airway
1. More rostral larynx
2. Relatively larger tongue
3. Angled vocal cords
4. Differently shaped epiglottis
5. Peds narrowest part is cricoid, adult is cords
Treatment for bronchospasm
Epi 0.1-0.5mg IV is definitive if you know pt is indeed in bronchospasm
Bones of Orbit
PFLEZMS

Palatine
Frontal
Lacrimal
Ethmoid
Zygomatic
Maxillary
Sphenoid
New name for bacteriodes
Prevotella

Melanogenica and intermedia
Danger Space
Between alar fascia and prevertebral fascia

superior- skull base

Inferior posterior mediastinum
Bone Scan
indium 111
technetium 99
TUGSE
Traumatic ulcerative granuloma with stromal eosinophilia

Lymphocytes, neutrophils, plasma cells, eosinophils, histiocytes
Bone within a soft tissue mass
Perifpheral ossifying f ibroma
strawberry gingivitis
large vessel vasculitis
nasal drainage
lethargy
Wegeners Granulomatosis

Oral manifestations rare
also involves kidneys, lungs
C-ANCA
TB treatment
RIPE for 6 weeks
then drop to Rifampin and isonizid for 6 months
presentation: tongue lesion with neck mass


Diffrential to remember: cat scrath..presents with neck mass but NO oral lesions in young kid
Granulomatous diseases
Sarcoid
TB
Fungal infections
Chrohns
Oro facial granulomatosous- dx of exclusion
cicatricial pemphigoid
oral and ocular (scarring) lesions
subepithelial clefting- separation of basement membrane
Markowitz Classification of NOE Fractures
I: Attached to large piece of bone
II: Comminuted but still attached to large piece of bone
III: Communuted and avulsed
Acetazolamide
Carbonic anhydrase inhibitor

decreases prodiction of HCO3

decreases intracranial hypertension
used for glaucoma
used for medical treatment of retrobulbar hematoma
Bone
Osteocytes- hypocellular - white spaces empty
Osteoblasts plump and lined up on surface of bone
Osteclasts

Trabeculae - spongy looking matrix
Eosinophilic

Looks like a sponge
Cartilage
Chondrocytes instead of osteocytes, larger
more myxoid/amphophilic (bluish)
more hypercellular

BLUE BACKGROUND

Pleomorphma Adenoma has a cartilagenous background
Nerve
Schwann cels- supporting cells
Axons- surrounded by myelin sheath

axons bundeled into nerve fibres surrounded by CT called endoneurium

those fibers are surrounded by perineurium and then THOSE fibers are bundled into fascicles

Grouping of fascicles form the nerve

Silver stain is used for nerves - S100 stain (brown)

on H and E, cells look spindle shapes
Fat
Meshwork of empty
Small inconspicuous adipocytes
Fibrous connective tissue septa separate lobules
Smooth Muscle
No cross striations
Surrounds blood vessels, GI tract, GU tract, Respiratory tract

Leiomyoma
Angionleiomyoma
Fibrous connective tissue
Collagen of varying densities
Ground substance- small proteins, water. looks more pale blue

collagen can be sclerotic, hyalinized
Peripheral giant cell granuloma
Only on alveolar ridge
cuz it originates from dental tissue - PDL
Peripheral ossifying fibroma originates from?
Also originates from PDL
4 P's of ginigiva/alveolar ridge
Pyogenic granuloma
Parulus
Peripheral ossifying fibroma
Peripheral giant cell granuloma
Keratoacanthoma
Sun exposure
lower lip
rough surface- warty
premalignant
old people
grow fast
looks like cancer (scca- keratocanthoma variant)
left alone...would regress
Nevus of Ota
Black sclera
Trigeminal distribution
Melanocytic Nevus
Common at birth
caucaisians
start out typocally flat and pigmented
as we age they start to raise up (mole)
can have normal adnexal skin structures- Hair
as we age, they depigment
Antoni A
Antoni B
Nerve tissue- Schwannoma

Antoni A is more organized nerve tissue with vercay bodies

Antoni B is more disorganized
schwannoma with ancient change
Looks ugly but just LOOKS wierd do to changes over time but you can find areas of classic schwannoma
Nasofrontal duct drainanage
Middle meatus
maxillary sinus drainage
Middle meatus
Drugs that cross the BBB
1) Cephalosporins:
eg. Ceftriaxone, Cefotaxime, ceftazidime, cefepime

2) Penicillins: Ampicillin

3) Antifungals: Amp B with flucytosine, Fluconazole

4) Vancomycin

5) Anti-tuberculous drugs. (eg. INH)
Indications for obliterations of sinus
Posterior wall fx
NOE fx
frontal sinus floor fracture
Most common causes of adult meningitis
strep pneumo
h flu
nisseria menningitis

treat with third generation ceph like cephtriaxone
Neurofibromatosis
2 or more Neurofibromas or 1 plexiform
6 or more Cafe Au laits
2 or more Lisch Nodules (pigmented iris hamartomas)
optic glioma
axillary freckling
first degree relative with NF-1
"comet shaped nuclei" and mast cells (fried egg with fine granules)
Treatment consists of biopsy
Cigar shaped nuclei
Smooth muscle
mass in FOM yellow in color looks like a stone
Lymphoepithelial cyst
Dermoid cyst
Epidermoid cyst
Lipo
Sialolith
MACHO
Differential for posterior mandible radiolucent lesions

Myxoma
Ameloblatoma
CGCG
Hemangionma
OKC
Multiple Myeloma workup
IgM markers
Bence jones proteins
Kappa lambda light chain protein
Bone scan technicium 99
Plasmacytoma
Remember the lesion s/p ext #19

radiolucent - use MACHO to diffrentiate
malignant disease
make sure to diffrentiate from multiple myeloma
resect as it is malignant disease
Multiple myeloma treatment
Treat with Thalidomide
Histoplasmosis
Ohio River Valley
Mississippi Valley
Characteristics of Malignancy
Increased nuclear size (with increased nuclear/cytoplasmic ratio--N/C ratio).

Variation in nuclear or cell size (pleomorphism).

Lack of differentiation (anaplasia).

Increased nuclear DNA content with subsequent dark staining on H and E slides (hyperchromatism).

Prominent nucleoli or irregular chomatin distribution within nuclei.

Mitoses (especially irregular or bizarre mitoses).
Granular cell tumor
Remember lesion on palate that looks spongy and red

look for Pseudoepitheliomatous Hyperplasia which is drops off the epitheilium

Common on tongue

Histologically looks very granular
debulk it (cus it passes the margins) and it usually doesnt come back
Features of dysplasia - architecture
Irregular eppithelial stratification
Loss of polarity of basal cells
DROP shpaed, rounded or bulbous rete ridges (not test tube like as normal)
increased numbers of mitotic figures
absnoramlly superficial mitosis
premature keratinization
keratin pearls within rete ridges
features of dysplasia - cytology
Abnormal variation in nuclear size
variation in shape
in cell size
cell shape
increased n to c ration
increased nucluear size
atypical mitotic figures
increased number and size of nucleoli
Verrucous carinoma - remember the lesion in the buccal vestible from denture wearing that looks like a yellow irregular plaque
Rete ridges broad and pushing
Lesion is described as rather boring because it is a low grade
not a highly dysplastic lesion so not very sensitive to radiation
should resect lesion but laser ablation and liquid nitrogen can also be done
Focal epithelial hyperplasia (hecks disease)
lesions on lips tongue etc
kids
native american anscestry
related to hpv 13 and 32
spontaneously regress
looks like neuromas in the mouth or sometimes condyloma like too
mom may have it too

Mitosoid cells
Proliferative Verucous leukolplakia - remember the lesion on the side of the tongue, dorsal, lateral and carrying on to the ventral
Diffuse white lesions on tongue, lips, gingiva, buccal mucosa
looks kind of like lichen planus
sometimes looks like a fungal lesion - can try antifungals first before doing biopsy
once diagnosed you can just watch and wait as sometimes there are so many lesions that develop
AE1/AE3 Stain
CAM 5.2
Stains epithelium brown
SMA stain
Stains Muscles
Ortho vs parakeratin
Parakeratin has nuclei with more even surface
Diffrential for squamous papilloma
Verruca
Condyloma
Verruciform Xanthoma
Focal epithelial hyperplasia (hecks disease)

Associated with HPV 6 and 11

Koilocytes
Verruca Vulgaris
HPV 2,4,6,40

Contageous

Skin of hands common

Treat with cryo or conservative excision

does not become malignant

Koilocytes
Condyloma acuminatum
High risk subtypes are 16 and 18

STD

Koilocytes
Koilocytes
Virus altered epithelial clear cells with small dark (pyknotic) nuclei. seen in prickle cell layer

surgical excision
or laser ablation (?? airborne spread)
Inverted Papilloma
Benign localized proliferation proliferation of the respiratory mucosa

Has a potential to become malignant

HPV 6,11,16

Median age 55 years

males

arises from lateral nasal cavity or antrum

has significant growth potential

histo- looks like big islands of cells
Molluscum Contagiosum
Usually kids and young adults

Warms parts of skin- neck, eyelids, trunk, genitals

Sexual contact, but also sharing clothing, communal bathing, etc

look like little CRATERS
histologically the craters in the middle are filled with bloated keratinocytes (molluscum bodies)

spontaneous remission in 6-9 months
cryo

NO potential for transformation
Seborrheic Keratosis
Benign proliferation of epidermal basal cells

Chronic sun exposure

Histo- hyperkeratotic, acanthosis, numerous
PSEUDOCYSTS

Common form in black people - Dermatosis papulosa nigra
Actinic Lentigo
Chronic sun

Looks like flatter seborrheic keratosis

histo- melanin laden basilar cells
Oral Melanocytic Macule
Flat brown mucosal discoloration caused by focal increase in melanin deposition and possibly and increase in melanocytes as well

Histo- increased melanin in the basal layes
Acquired Melanocytic Nevus
MOLE
Absolute health contraindications to surgery
MI less than 1 month
De compensated CHF
Acute coronary syndromes
HTN urgency/emergency
Severe valvular disease
severe arrhythmia
Ketamine effects on BP
Increases
General Asthma Meds
Beta Agonists
Long Acting
Short Acting
Inhaled Corticosteroids
Leukotriene Receptor Blockers
Anticholinergic meds
Classes of asthma of FEV
Mild Intermittent >80%

Mild Persistent >80%

Moderate Persistant 60-80%

Severe <60%
Pain and sedation meds to avoid in asthma (3)
Beta blockers
Toradol
Morphine (histamine release)
Lantus vs lispro vs NPH in duration
Lantus long
Lispro short
NPH intermediate

for sedations always continue long acting (usually night before)
half of intermediate
hold short acting
and then cover post op with sliding scale

Oral hypos should be held in AM for surgery
Diabetes diagnosis
Random > 200
fasting >126
MELD
Model for end stage renal disease

Score of < 10 okay for elective sx
>15 no surgery


5 Components
Age
Bilirubin
Creatinine
INR
Dialysis
Normal GFR
120 ml/min
DDAVP dosing for HF A
30micrograms/kg in saline solution
Most common causes of thrombocytopenia in surgical pt
Sepsis
DIC
Heparin
H2 Blockers
Certain ABX
Massive Transfusion
Indications for trach
1. Unable to orally intubate
2. Tumor
3. Emergent Airway
4. Prolonged intubation
Indications for intubation
Hypercarbia PCO2 > 55
Hypoxia PO2 < 60
Unable to hold secretions
Unable to protect airway
Whats different about cricoid cartilage
only ones that go completely around
Inferior Strap Muscles
Streno hydoid
Sterno thyroid
thyrohydoid
omohyoid
Layers to trach
Skin
Subq
Strap
thryoid fasicia
throid isthmus
pretracheal fascia
trach
Trach tubes
Shileys (brand) come in 4, 6 or 8

cuffed, non fenestrated
men ususally 8
women usually 6
Carnoys solution
Carnoy's solution is a fixative composed of 60% ethanol, 30% chloroform and 10% glacial acetic acid.[1]

Carnoy's Solution is composed of:

1 g of ferric chloride (FeCl3) dissolved in 24 mL of absolute alcohol
12 mL of chloroform
4 mL of glacial acetic acid
Townes View
30 degress upward pointing to glabella (hariline)

shows lateral medial condyle position
Wharthins Tumor
Papillary Cystadenoma Lymphomatosus

MOstly parotid

ALOT of times bilateral but metachrounous

associated with SMOKING (8 fold increase)

histology- look for papillary projections, yst like structures and palisading lining. pretty distinct look

6-12% recrrence rate and remember it can later present on the other side
Polymorhous low grade adenocarcinoma
minor salivary glands

classic is palate

swiss cheese look on low power

differentiated from adenoid cystic on high power because it shows cord like architecture

also shows perineural invasion like adenoid cystic

recurrence rate is
Enamel organ forms....
Enamel
Dental papilla forms....
dentin and pulp
inner enamel epithelium forms...
ameloblasts
OKC's
Hyperchromatic
palisading nuclei
parakeratin
6-8 cells thick
Gingival cyst of adult
soft tissue lateral perio cyst counterpart

look for "speedbumps" in the cyst lining

can be "botryoid"
Ameloblastic Fibroma
Look for "islands" of epithelium in a fibrous background (denta papilla background)
Dentigerous cyst versus aot on radiograph
cyst attaches at cej in DC while it attaches at midroot on AOT
Langerhans histiocytisis
Gingival appearance
Teeth floating in space
Lots of eosinophils
Histoplasmosis
Birds and bats
Ohio river valley
Pigeons
4 P's
Pyogenic granulona
Peripheral giant cell
Peripheral ossifying fibroma
Peripheral fibroma
Plasmacytoma stain
CD 138

If localized then radiation is treatment of choice but rarely curative. Usually develops into multiple myeloma
What causes cleft palate?
failure of fusion of medial nasal prominence and maxillary prominence. usually happens at 4-8 weeks
Cleft lip repairs
Tennison Randall - z plasty across philtrum

Millard (remember "c flap" is to lengthen columella)
cleft palate repairs
Manchester

Millard - sacrifice prolabium and use tissue from lip
submucous cleft classic sign
bifid uvula

important because 1/3 require surgery for speech issues
Binder syndrome classic sign
absence of ANS
Most basic dx of tmj
Muscular pain
Joint pain
Both most
Questions to ask for tmj
Ttp
Pain on loading (opposite side usually hurts)
Joint noises
Muscles of mastication
ROM - with pain, wo pain, lateral and protrusive (10mm each)
Evaluate teeth- wear facets, cross bites, interferences
Tmj imaging
Pano
MRI
CT
RADIONUCLEIDE
Tmj diff dx
Myofascial pain
Internal derangement
Wilkes
I Painless click
II Painful click
III Intermittent lock, pain
IV Closed lock, chronic pain
V Crepitus, perforation, chronic pain
PVL
High grade dysplasia
Multiple diffuse lesions
Leukoplakia with papillomas on side of tongue

Diffuse white plaques on gingiva (bad)
Pyostomatitis vegetans
Yellowish linear Pustules in a red mucosal background on the gingiva

Unusual oral expression of inflammatory bowel disease

Snail track ulcerations

Colbetasol
Amyloid like material
think CEOT
Ghost cells
Calcifying odontogenic cyst