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Physical Diagnosis 2 Exam 1 · Class of 2028

Physical Diagnosis 2 Exam 1 Cram Sheet

The encounter, the oral presentation and documentation; the skin — structure, the descriptive vocabulary, abnormal findings of skin, hair and nails, and the examination itself; then the advanced ocular and ENT examinations.

How to use this: this is a condensed, night-before-the-exam reference, not a replacement for the full study guide — it assumes you've already learned the material and just need the highest-yield facts at a glance. If a term feels unfamiliar, go back to the full guide for the explanation.

The Encounter, Presentation & Documentation

TermWhat you need to know
Oral presentation — openingOpen with the past medical history and the chief complaint. Then pertinent positives and negatives from BOTH history and physical. Follow mostly the order you obtained them. Try not to read your notes.
Oral presentation — the testA good presentation leads your facilitator to the same differential you formulated. It is a well-organized vignette, not the written note read aloud; the goal is to help listeners visualize the patient.
Focused vs comprehensiveA focused encounter narrows BOTH the history and the examination — history of present illness, review of systems, past medical history, social history, family history, medications and allergies are all focused. It is not a comprehensive encounter written up more briefly.
Focused encounter — required outputDifferentials, laboratory and imaging studies, a diagnosis, and a treatment plan including patient education. Narrowing the data gathered does not narrow what you must conclude.
History and physical vs SOAPThe history and physical is comprehensive (whole history, head-to-toe). The SOAP note is problem-focused: Subjective (what the patient said), Objective (what you found, always with a general impression), Assessment (what you concluded), Plan (what you will do).
Documentation rules that cost marksDescribe findings — never 'normal', 'abnormal' or 'unremarkable'. NO abbreviations, with no exceptions. Keep subjective and objective in their own sections. If you did not do it, document why — never invent a finding. Never write a note with another student.
CommunicationAdapt style and content for each patient. When someone else supplies the answers, ALWAYS look at and interact with the patient, not the person answering. Accept feedback and modify behavior; different facilitators give different feedback, and that is expected.

Skin — Structure & Function

TermWhat you need to know
Five functionsProtection of internal structures · prevention of entry of microorganisms · temperature regulation · excretion · production of vitamin D.
Sudoriferous (eccrine) glandsSecrete sweat to maintain body temperature.
Apocrine glandsBecome active during PUBERTY; secrete pheromones.
Sebaceous glandsSurround hair follicles; secrete sebum to keep hair and skin moist.
Vellus vs terminal hairVellus is short, fine hair covering the body. Terminal is coarse — scalp, pubic, axillary, beard.

Descriptive Vocabulary — Distribution & Configuration

TermWhat you need to know
Five features of any lesionDistribution (location) · configuration (shape) · morphology (form and structure) · color · texture.
Distribution → diagnosisGeneralized/diffuse = allergic reactions. Regional = tinea capitis. Sun-exposed (photodistribution) = skin cancers. Dermatome = herpes zoster. Extensor = psoriasis. Flexor = intertrigo. Intertriginous = skin creases and folds.
Configuration termsAnnular = ring. Arciform = arcs or curves. Confluent = run together. Discrete = remain separate. Grouped = a cluster. Gyrate = twisted, coiled, spiral. Iris/target = bull's eye. Linear = line or stripe. Reticular = lacy or networked. Serpiginous = snake-like.
Herpetiform vs zosteriformHerpetiform = grouped papules or vesicles arranged as in herpes SIMPLEX. Zosteriform = clustered in a DERMATOMAL distribution, as in herpes zoster. The pair most often swapped.
Primary vs secondary lesionPrimary forms first and results directly from the disease — identifying it is the key to the whole description. Secondary is a change in the primary over time, from disease progression, TREATMENT, or MANIPULATION (picking, scratching).

Primary & Secondary Morphology

TermWhat you need to know
The 1 cm hinge — three matched pairsFlat: macule (<1 cm) / patch (>1 cm). Solid elevated: papule (<1 cm) / plaque (>1 cm). Fluid-filled: vesicle (<1 cm) / bulla (>1 cm). Six terms from three pairs — this is why a ruler is on the equipment list.
Nodule vs papule vs tumorNodule: elevated, firm, circumscribed, round or ellipsoid, DEEPER in the dermis than a papule, 1–2 cm (Bates: >0.5 cm). Tumor: solid mass >2 cm. Papule: solid, <1 cm.
PlaqueElevated, flat-topped, firm, rough; plateau-like, occupying a large area compared with its elevation; >1 cm; may be coalesced papules. Example: psoriasis.
Wheal, pustule, cystWheal: elevated irregular cutaneous edema, solid, TRANSIENT, variable diameter (the only transient one). Pustule: superficial elevation filled with PURULENT material, usually <1 cm. Cyst: elevated, circumscribed, ENCAPSULATED, in dermis or subcutis, liquid or semisolid (the only encapsulated one).
Erosion vs ulcerErosion: loss of superficial epidermis, does NOT involve dermis; moist but does NOT bleed. Ulcer: deeper loss of epidermis and/or dermis; MAY bleed and scar. Depth determines all three consequences at once.
Crust, fissure, scale, excoriationCrust: cellular debris, dried serum and blood — a scab; antecedent lesion usually a vesicle, bulla or pustule. Fissure: linear crack (athlete's foot). Scale: thin flake of exfoliated epidermis (dandruff). Excoriation: abrasion or scratch mark, linear or rounded.
Scar vs keloidScar (cicatrix): fibrous tissue replacing destroyed tissue; hypertrophic = thick and pink, atrophic = thin and white; does NOT extend beyond the injured area. Keloid: a scar that GROWS BEYOND the wound.
Lichenification & collarette scaleLichenification: thickening with skin line accentuation from chronic irritation (atopic dermatitis). Collarette scale: fine scale peripherally attached and centrally detached at a lesion's edge (pityriasis rosea).
Corn vs callus; wartsCorn: smaller, usually over a NON-weight-bearing area of the foot, conical keratin pointing toward the dermis. Callus: thickened epidermal keratin, usually on the sole at ball or heel. Verrucae (warts) are caused by human papillomavirus.

Abnormal Findings — Skin, Hair & Nails

TermWhat you need to know
DiascopyPress clear glass or plastic against the skin and look at the lesion under pressure. Color FADES = vascular engorgement. Does NOT fade = hemorrhage in the skin.
Petechiae / purpura / ecchymosisSame finding at three sizes, NONE blanching. Petechiae <3 mm. Purpura 3 mm–1 cm. Ecchymosis >1 cm, purple or purplish-blue, fades over time.
Angiomas & telangiectasiaCherry angioma (Campbell De Morgan spots): dome shaped, bright red to violet/black, ± blanching. Telangiectasia: fine irregular vessels, blanches. Spider angioma: central red macule with radiating arms, blanches.
Triple response of LewisFirm stroking (dermatographism) produces: initial red line (capillary dilatation) → reflex flare with broadening erythema (arteriolar dilatation) → linear wheal (transudation of fluid, i.e. edema).
Pressure ulcer stagesI: INTACT skin, erythema failing to blanch, plus change in temperature, consistency, sensation, color. II: PARTIAL thickness loss (epidermis, dermis or both). III: FULL thickness, subcutaneous necrosis, may extend to but NOT through muscle. IV: full thickness with destruction of tissue, muscle and/or bone.
Tinea by siteCorporis (body) · pedis (foot) · barbae (beard) · cruris (groin) · capitis (scalp) · unguium (nails). Pedis: dry/scaling or macerated fissuring of interdigital spaces. Corporis: sharply demarcated round plaques with CENTRAL CLEARING. Capitis: round scaling patches of alopecia, hairs broken off close to scalp.
Skin malignanciesBasal cell carcinoma: face; translucent PEARLY nodule, depressed center, raised borders; may ulcerate; non-healing ulcer. Squamous cell carcinoma: face and sun-exposed; red scaling, crusting nodule or plaque that ulcerates and bleeds. Melanoma: irregularly colored plaque with sharp notches and pigment variation.
Melanoma warning lettersA asymmetry or shape · B border irregularity · C color variation · D diameter larger than 6 mm · E evolving, elevation · F family history · G growing.
Kaposi's sarcomaThe most frequent neoplasm in patients with acquired immunodeficiency syndrome. Light-colored lesions coalescing into darker ones; dark blue-purple macules, papules, nodules and plaques; widely disseminated on legs, trunk, arms, neck and head.
Patchy hair loss — three causesTinea capitis: SCALING patches, hairs broken close to scalp. Alopecia areata: round patches, 'EXCLAMATION POINT' hairs, chronic inflammatory disease of follicles, associated with autoimmune disorders. Trichotillomania: from an urge to pull, single or multiple patches. Also: androgenic alopecia = male pattern baldness; hirsutism = increased hair in women in a male pattern.
Nail findingsKoilonychia: spoon-shaped concave, plate thins and inverts. Onycholysis: PAINLESS separation of plate from bed starting DISTALLY (chemicals, immersion, fungal, psoriasis, tetracycline, trauma). Pitting: dystrophy of the plate. Terry's nails: proximal white, distal dark. Green = pseudomonas. Brown–black = MELANOMA.
Nail lines, hemorrhages, clubbingBeau's lines: transverse DEPRESSIONS — halfway up the nail suggests illness about 3 MONTHS ago. Mee's lines: transverse lines. Splinter hemorrhages: distal capillary loop. Subungual hematoma: hemorrhage to the nail plate. Clubbing: nail base-to-finger angle GREATER THAN 180°, fingertip rounded and bulbous. Paronychia: soft tissue infection at cuticle or nail fold; acute is painful and purulent.

Performing the Skin Examination

TermWhat you need to know
IPPAInspection, palpation, percussion, auscultation — the same order for EVERY body system except the ABDOMINAL examination. Some systems do not use all four.
Equipment & environmentRuler, light source, magnifying lens, gloves for open lesions. Patient in a gown so hair, anterior and posterior surfaces, palms and soles, nails and interdigital spaces can all be inspected. Good light, preferably NATURAL — artificial light may distort skin tone.
Six characteristics assessedColor · moisture (dryness, sweating, oiliness) · temperature (warmth, coolness) · texture (roughness, smoothness) · mobility and turgor · lesions.
Temperature techniqueUse the DORSAL aspect of the hands.
Mobility vs turgorMobility: normal skin lifts with ease; reduced mobility = EDEMA. Turgor: normal skin quickly resumes its shape; skin that remains elevated = DEHYDRATION.
Central vs peripheral cyanosisCentral: often inadequate oxygenation IN THE LUNGS. Peripheral: usually inadequate CIRCULATION. Same color, different organ.
Hair & scalpInspect color, distribution and quantity; palpate for texture. Separate the hair into sections to see the scalp, and inspect BEHIND THE EARS and the OCCIPUT. Should be clean — no lesions, discolorations, flaking or parasites. A magnifying glass aids inspection for lice (nits are tiny white ovoid granules adherent to hairs).
Pruritus is not a diagnosisIt is the sensation causing the desire to scratch. Generalized itching with no obvious reason: dry skin, aging, pregnancy, uremia, jaundice, lymphomas, leukemias, drug reaction, lice.
History — bugs, drugs, contactBugs: family members or contacts with the same, travel. Drugs: systemic medications, over-the-counter AND prescription. Contact: allergens and irritants from hobbies, occupation, environment. Core questions: where it first appeared, what it looked like, how it progressed, associated symptoms, what treatment was tried.

★ WHAT SHE TOOK OUT OF SCOPE

TermWhat you need to know
The named virus in viral conjunctivitis“I'm not going to test you on it, but adenovirus…” — she uses it for the great-mimicker story. NOTE: CMS I Exam 2 DOES test adenovirus. Different course.
The exophthalmometer“I am not going to test you on the minutia of how to do that test… it was 20 to 22 millimeters… DON'T WORRY ABOUT IT.” BUT RECOGNIZING EXOPHTHALMOS IS IN — “about exophthalmos and how to recognize it.”
The strabismus diagram“This is just a visual… that you don't have to memorize.” ESO-, EXO- and HYPERTROPIA as concepts stay in.
The corneal reflection test“We've already done this, so I'm not gonna test you on it… we already did that in PD1.”
The Adie's pupil look-alikesDysautonomia/POTS, Shy-Drager, diabetes, amyloidosis — “it's not on my test this time.” BUT ADIE'S PUPIL ITSELF IS IN: “you should know Adie's pupil, that could be on my test.”
The Latin behind OD/OS/OU“I don't care if you remember Oculus Sinister or Dexter.” BUT THE ABBREVIATIONS ARE IN — “those are terms that you must remember.” OD RIGHT · OS LEFT · OU BOTH.

★ “VERY IMPORTANT TO COMMIT TO MEMORY”

TermWhat you need to know
DIPLOPIA and the cranial nervesHORIZONTAL (images SIDE BY SIDE) = palsy of CN III or VI. VERTICAL (images ON TOP of each other) = palsy of CN III or IV. Her shortcut: “THREE FOR BOTH OF THOSE” — CN III is in both patterns; side-by-side is where CN VI joins in.
The RED-EYE CHART — “be very familiar with that chart”It is a PICTURE on the slide, so it is in no text copy of the deck. Written out in full in the study guide. Scan it by COLUMN: pattern of redness, pain, vision, discharge, pupil, cornea, significance.
RED TEXT ON A SLIDE“See how this is in red — red's important too.” Said of: an ACUTE, SIGNIFICANTLY DILATED PUPIL IS A MEDICAL EMERGENCY, particularly with headache or neurologic signs — UNCAL HERNIATION or POSTERIOR COMMUNICATING ARTERY ANEURYSM.
THE REFERRAL LIST — “please know this list”Her reason: “because you're going to be making those dispos.” EMERGENT (ophtho/ER IMMEDIATELY): SUDDEN VISION LOSS · RETINAL ARTERY OCCLUSION · CHEMICAL BURNS · RUPTURE · ACUTE ANGLE-CLOSURE GLAUCOMA · VITREOUS HEMORRHAGE. URGENT (ophtho in A DAY OR LESS): ACUTE GLAUCOMA · ORBITAL CELLULITIS · CORNEAL ULCER OR ABRASION · RETINAL DETACHMENT · MACULAR EDEMA OR HEMORRHAGE · HYPHEMA.

History & Symptom Patterns

TermWhat you need to know
The four axesTIME COURSE · PRECIPITATING FACTORS · PALLIATIVE/EXACERBATING VARIABLES · VISION LOSS.
Laterality and floatersBILATERAL visual loss → NEUROLOGIC, not ophthalmologic. MULTIPLE NEW flashes/floaters → RETINAL TEAR or VITREOUS HEMORRHAGE. A SINGLE floater → probably benign.
TempoRAPID deterioration → VASCULAR. GRADUAL → CATARACT and the like.
The anesthetic testPain RELIEVED by topical anesthetic → a SURFACE problem (corneal injury). NOT relieved → a DEEPER source.
Four symptom patternsACUTE/UNILATERAL/PAINLESS → retinal vascular occlusion, detachment, vitreous hemorrhage, macular degeneration. ACUTE/UNILATERAL/PAINFUL → cornea + anterior chamber: abrasion/ulcer, uveitis, traumatic hyphema, acute narrow angle glaucoma. ACUTE/BILATERAL/PAINFUL → THERMAL, RADIATION or CHEMICAL. GRADUAL/PAINLESS → simple glaucoma or cataract.
Eye pain, qualifiedWith BLINKING → abrasion or foreign body. GRITTY → conjunctivitis. + PHOTOPHOBIA → iris inflammation. + HEADACHE → acute narrow angle glaucoma. On EYE MOTION → optic neuritis. + TEMPORAL pain → temporal arteritis.
DischargeWATERY or MUCOID → allergic or viral. PURULENT → bacterial.
Don't forget to askTETANUS STATUS in eye trauma. ACID OR ALKALI after a chemical splash. Systemic: DIABETES, HYPERTENSION and HIV — “HIV is going to affect basically any type of etiology.”

Inspection

TermWhat you need to know
Order of the examINSPECTION → external → cornea/lens/pupils → VISUAL ACUITY (“the vital sign of the eye”) → VISUAL FIELDS → OCULAR MOTILITY → PUPILLARY REACTIONS (CHECK BEFORE DILATING) → corneal reflection → special tests → slit lamp → pressure → ophthalmoscopy.
In traumaDO NOT PALPATE THE GLOBE.
Lid and brow signsSCALY brows → seborrheic dermatitis. LATERAL SPARSENESS → HYPOTHYROIDISM. PTOSIS → myasthenia gravis, CN III damage, or sympathetic damage (HORNER); senile = weak muscle + relaxed tissue + herniated fat weight. XANTHELASMA on the NASAL lid → lipid disorders.
HORDEOLUM vs CHALAZION on inspectionHORDEOLUM: PAINFUL, AT THE LID'S EDGE. CHALAZION: chronic, NON-painful, meibomian, generally NOT at the margin — POINTS INSIDE THE LID.
Sclera colorYELLOW → LIVER DISEASE. BLUE → OSTEOGENESIS IMPERFECTA.
Proptosis techniqueSTAND BEHIND THE SEATED PATIENT AND LOOK DOWN FROM ABOVE, drawing the lid slightly up. Causes: retrobulbar hemorrhage, orbital cellulitis, orbital tumor, GRAVES.
Nasolacrimal duct testLook UP; press the lower lid near the MEDIAL CANTHUS just inside the bony rim; watch for regurgitation from the puncta. MUCOPURULENT FLUID = OBSTRUCTION. AVOID if significantly inflamed or tender.
Everting the upper lidLook DOWN and relax → raise the lid so lashes protrude → grasp and pull DOWN AND FORWARD → stick AT LEAST 1 cm ABOVE THE MARGIN at the upper tarsal border → push down as you raise the edge. DO NOT PRESS ON THE EYEBALL. NEVER EVERT IF GLOBE RUPTURE IS SUSPECTED.
Subconjunctival hemorrhage on examPAIN ABSENT · VISION AND PUPIL UNAFFECTED · NO DISCHARGE · CORNEA CLEAR. GLOBE RUPTURE MORE LIKELY in trauma and when the hemorrhage ENCIRCLES THE ENTIRE CORNEA.
Injection patternDIFFUSE, MAXIMAL PERIPHERALLY → conjunctivitis. JUST AROUND THE CORNEA → KERATITIS, IRITIS or ACUTE GLAUCOMA.

Acuity, Fields & Motility

TermWhat you need to know
OD / OS / OUOD = RIGHT eye. OS = LEFT eye. OU = BOTH. “Terms that you must remember.”
20/200At 20 FEET the patient reads print a NORMAL eye reads at 200 FEET. THE LARGER THE SECOND NUMBER, THE WORSE THE VISION. Cannot read the chart → document COUNTING FINGERS, HAND MOTION, or LIGHT PERCEPTION.
PINHOLE TESTAdmits only light PERPENDICULAR to the lens, so it need not be bent → CORRECTS ANY REFRACTIVE ERROR. NOT corrected → consider CATARACT, OPTIC NERVE DISEASE or RETINAL DISEASE.
Confrontation fieldsSTATIC FINGER WIGGLE (arm's length, hands 2 ft apart lateral to the ears, into center of view, each quadrant) PLUS KINETIC RED TARGET (5 mm red-topped pin inward from beyond each quadrant — ask when it FIRST APPEARS RED).
Blind spot15 DEGREES TEMPORAL to the line of gaze. ENLARGED in GLAUCOMA, OPTIC NEURITIS and PAPILLEDEMA. A temporal defect in one eye → TEST FOR A NASAL DEFECT IN THE OTHER.
NystagmusA FEW BEATS ON LATERAL GAZE IS NORMAL. Bring the finger back into BINOCULAR vision — if it persists there, consider NEUROLOGIC disease.
Lid lagRim of SCLERA VISIBLE ABOVE THE IRIS on DOWNWARD gaze. Most often HYPERTHYROIDISM.

The Pupils

TermWhat you need to know
Anisocoria½ to 1 mm difference is COMMON and BENIGN IF THE REACTIONS ARE NORMAL. ABNORMAL: difference > 1 mm, or a POORLY REACTIVE pupil.
SWINGING LIGHT TESTIndication: ANISOCORIA. ABNORMAL = PARADOXICAL DILATION OF BOTH PUPILS when the light swings to the affected eye, WITH AN INTACT CONSENSUAL REFLEX = RELATIVE AFFERENT PUPILLARY DEFECT = MARCUS GUNN PUPIL = THE LESION IS THE OPTIC NERVE. Mechanism: reduced afferent input → reduced efferent output to BOTH pupils → net dilation.
ADIE'S TONICLARGE, regular, usually UNILATERAL. Light reaction SEVERELY REDUCED/ABSENT. NEAR REACTION PRESENT BUT VERY SLOW. Degeneration of the CILIARY GANGLIA and POSTGANGLIONIC PARASYMPATHETIC fibers.
ARGYLL ROBERTSONSMALL, UNEQUAL, IRREGULAR. “ACCOMMODATES BUT DOESN'T REACT.” Classically TERTIARY SYPHILIS, today more often DIABETES; also LYME. Mydriatics dilate it only INCOMPLETELY.
HORNER SYNDROMEPTOSIS · MIOSIS · ANHIDROSIS of the ipsilateral face. THE SMALL PUPIL STILL REACTS BRISKLY to light and near — that is what separates it. Sympathetic supply to pupil AND levator interrupted. CONGENITAL: involved iris is LIGHTER (heterochromia).
CN III PALSYDILATED pupil FIXED to BOTH light and near, with PTOSIS and LATERAL DEVIATION almost always present.
Three causes of a dilated pupilOnce local eye disease is excluded: (1) COMPRESSION/LESION OF CN III · (2) PARASYMPATHETIC DENERVATION from a ciliary ganglion lesion = ADIE'S · (3) PHARMACOLOGIC BLOCK of the sphincter.
Oblique lighting — crescent shadowLight from the TEMPORAL side. NO SHADOW = normal, flat iris, OPEN angle. A SHADOW on the MEDIAL side = iris BOWED FORWARD = NARROW ANGLE = raised risk of NARROW-ANGLE GLAUCOMA.
Corneal scar vs cataractSCAR: SUPERFICIAL grayish-white corneal opacity. CATARACT: DEEPER, visible ONLY THROUGH THE PUPIL.

Fundoscopy & Trauma

TermWhat you need to know
DO NOT DILATE if…SERIAL NEUROLOGIC EXAMS are required · ELDERLY PATIENTS WHO HAVE HAD CATARACT SURGERY · SUSPECTED ACUTE ANGLE-CLOSURE GLAUCOMA. If you dilate: DOCUMENT THE TIME AND THE AGENTS.
NORMAL fundusYELLOWISH-ORANGE TO CREAM · small disc vessels · SHARP disc margin · cup CENTRAL or slightly TEMPORAL, diameter LESS THAN HALF the disc.
PAPILLEDEMARAISED INTRACRANIAL PRESSURE. PINK, disc SWOLLEN with BLURRED MARGINS, CUP NOT VISIBLE, LOSS OF VESSEL PULSATIONS.
GLAUCOMATOUS CUPPINGCup ENLARGED, MORE THAN HALF the disc diameter; retinal vessels SINK IN AND AROUND the disc.
OPTIC ATROPHYWHITE disc, TINY DISC VESSELS ABSENT — death of optic nerve fibers. Seen in OPTIC NEURITIS, MULTIPLE SCLEROSIS, TEMPORAL ARTERITIS.
Trauma mechanicsLARGER objects transfer most energy to the ORBITAL RIM; SMALLER objects may strike the GLOBE directly.
ORBITAL (BLOW-OUT) FRACTURESUNKEN EYE · INFRAORBITAL HYPOESTHESIA (infraorbital nerve) · DIPLOPIA PARTICULARLY ON UPWARD GAZE · decreased motility · sometimes IPSILATERAL NOSEBLEED. Look for ECCHYMOSIS, POINT TENDERNESS, PALPABLE STEP-OFF.
ZYGOMATIC FRACTUREFLATTENING OF THE MALAR EMINENCE, best seen from BEHIND the seated patient looking down. PAIN ON OPENING THE MOUTH because TEMPORALIS passes MEDIAL to the arch and inserts on the MANDIBLE.
HYPHEMABlood in the ANTERIOR CHAMBER from blunt trauma. Check ACUITY · PUPILS (crescent-like iris defect if torn) · RED REFLEX · INTRAOCULAR PRESSURE · SLIT LAMP.
CORNEAL ABRASIONEVERT THE UPPER LID — a foreign body in the upper tarsal conjunctiva scratches with every blink. A HAZY CORNEA SUGGESTS BACTERIAL INFECTION. TOPICAL ANESTHETIC IS FOR DIAGNOSIS, NOT TREATMENT.
CORNEAL ULCERHERPES SIMPLEX ULCERS ARE NOT VERY PAINFUL. Ophthalmoscope at +40 DIOPTERS may reveal it, but FLUORESCEIN IS MORE SENSITIVE for early ulcers. Fluorescein is taken up by cornea DEVOID OF EPITHELIUM.

★ TUNING FORKS — WORTH THREE POINTS

TermWhat you need to know
Why this block leads“The Weber and the Rinne tests are BOTH HIGH YIELD … the difference between sensorineural and conductive hearing loss is ALSO HIGH YIELD … IT WILL BE THREE POINTS ON TEST DAY.”
The two mnemonics, verbatim“RINNE IS UNDER THE PINNA” — the pinna is the outside of the ear, the Rinne fork goes on the MASTOID under it. “WEBER TELLS YOU WHETHER” — whether it is the RIGHT or the LEFT.
WEBER — where and what forFork on the TOP OF THE HEAD or MID-FOREHEAD. Evaluates UNILATERAL loss by LATERALIZATION. Normal = MIDLINE or equal in both ears.
WEBER in CONDUCTIVE lossLateralizes to the IMPAIRED ear. WHY: the block screens out room noise on that side, so the bone-conducted tone has that ear to itself.
WEBER in SENSORINEURAL lossLateralizes to the GOOD ear. WHY: inner ear or cochlear nerve damage impairs transmission on the affected side however the sound arrives.
RINNE — how, in orderFork on the MASTOID until the sound STOPS → move it CLOSE TO THE CANAL → ask if still heard. Bone conduction FIRST, air conduction SECOND.
RINNE normalAIR > BONE. A sound beside the ear is louder than one against the skull.
RINNE in CONDUCTIVE lossBONE ≥ AIR (abnormal). Vibration through bone BYPASSES the blocked external or middle ear and reaches an intact cochlea.
RINNE in SENSORINEURAL lossAIR > BONE — THE NORMAL RATIO PREVAILS. Rinne compares two routes to the SAME cochlea; damage degrades BOTH, so the ratio survives. Counterintuitive, and that is the test working.
★ THE WORKED CASERinne right = NORMAL. Weber lateralizes RIGHT. Which ear has sensorineural loss? THE LEFT. Normal Rinne rules out conductive on the right; Weber goes AWAY from a sensorineural lesion.
What the forks CANNOT doThey do NOT distinguish normal from BILATERAL sensorineural loss, and NOT normal from MIXED loss. Both tests work by COMPARING — a symmetrical loss looks normal.
The fork itself512 Hz — THE SMALLER ONE. Quiet room. Tap or “pinch” the fork.

Conductive vs Sensorineural — the whole table

TermWhat you need to know
SiteCONDUCTIVE: external or middle ear. SENSORINEURAL: inner ear (cochlea) or CN VIII / central pathways.
MechanismCONDUCTIVE: defective sound TRANSMISSION to the oval window. SENSORINEURAL: DESTRUCTION of hair cells or auditory nerve fibers.
Age of onsetCONDUCTIVE: childhood to about 40. SENSORINEURAL: MIDDLE OR LATER YEARS.
Visible on otoscopy?CONDUCTIVE: usually VISIBLE — EXCEPT OTOSCLEROSIS. SENSORINEURAL: NOT visible. Otosclerosis is the conductive cause behind a normal-looking drum.
Noisy environmentsCONDUCTIVE: hearing SEEMS TO IMPROVE (the block attenuates the background too). SENSORINEURAL: WORSENS.
★ The patient’s own VOICECONDUCTIVE: voice stays SOFT — inner ear and cochlear nerve intact, so they hear themselves fine. SENSORINEURAL: voice may be LOUD — they cannot hear themselves. A feedback loop, and a free bedside sign.
FrequenciesSENSORINEURAL: HIGHER REGISTERS LOST, so sound is distorted. PRESBYCUSIS = high-frequency loss.
CONDUCTIVE causesCerumen · foreign bodies · effusions · EXOSTOSES/OSTEOMAS (benign bony canal growths) · tumors · TM perforation · otosclerosis.
SENSORINEURAL causesCongenital · hereditary · PRESBYCUSIS · viral (RUBELLA, CYTOMEGALOVIRUS) · Ménière · NOISE · ACOUSTIC NEUROMA.
Whispered voice testTWO FEET BEHIND the patient (no lip reading), OCCLUDE the other ear, THREE-item sequence in a quiet whisper, TWICE. NORMAL = 3 or more of 6 correct. ABNORMAL = 4 of 6 INCORRECT.
Other bedside screensFINGER RUB and a WATCH.

The Vertigo Table

TermWhat you need to know
How to read itDURATION column first, then HEARING. Those two separate all six.
BENIGN POSITIONAL VERTIGOSudden, on ROLLING ONTO THE AFFECTED SIDE or tilting the head up. SECONDS TO UNDER A MINUTE per episode; the CONDITION lasts a few weeks and may recur. Hearing NOT affected. Tinnitus ABSENT.
VESTIBULAR NEURONITIS (acute labyrinthitis)Sudden. HOURS TO TWO WEEKS; may recur over 12–18 months. Hearing NOT affected. Tinnitus ABSENT. Nausea, vomiting, nystagmus.
MÉNIÈRE DISEASESudden. SEVERAL HOURS TO A DAY OR MORE, recurrent. SENSORINEURAL loss that recurs and eventually PROGRESSES. Tinnitus PRESENT and FLUCTUATING. PRESSURE OR FULLNESS in the affected ear.
DRUG TOXICITYInsidious or acute — LOOP DIURETICS, AMINOGLYCOSIDES, SALICYLATES, ALCOHOL. May or may not be reversible; partial adaptation. Hearing MAY be impaired.
ACOUSTIC NEUROMAInsidious, from CN VIII compression (vestibular branch). Variable duration. Hearing IMPAIRED ON ONE SIDE. Tinnitus PRESENT. MAY INVOLVE CN V AND VII.
CENTRAL VERTIGOOften sudden — BRAINSTEM LESION, ATHEROSCLEROSIS, MULTIPLE SCLEROSIS, VERTEBROBASILAR MIGRAINE, TIA. Variable but RARELY CONTINUOUS. Hearing NOT affected. Tinnitus ABSENT. OTHER BRAINSTEM DEFICITS — dysarthria, ataxia, crossed motor/sensory.
Hearing is the great dividerOf the six, only MÉNIÈRE, DRUG TOXICITY and ACOUSTIC NEUROMA touch hearing.
“DIZZINESS” splits FOUR waysVERTIGO (spinning) · PRESYNCOPE (faint/lightheaded) · DISEQUILIBRIUM (unsteadiness/imbalance) · PSYCHIATRIC (anxiety, depression, alcohol/substances). The word means NOTHING until the patient explains it.
TinnitusSound with NO EXTERNAL SOURCE. WITH hearing loss AND vertigo = MÉNIÈRE.

Ear Exam & Otoscopic Findings

TermWhat you need to know
Before the otoscopeInspect and palpate the AURICLES, MASTOID and TRAGUS.
Otoscopy techniquePull the auricle UP, BACK AND AWAY FROM THE HEAD. LARGEST speculum that fits. ULNAR ASPECT of the hand contacts the patient (anchors the instrument). INSUFFLATE.
Why the LARGEST speculumInsufflation needs a SEAL. A small speculum leaks and the test becomes uninterpretable.
Leak check BEFORE insertingAttach the speculum, put a FINGER OVER THE TIP, squeeze the bulb — you should FEEL PRESSURE BUILD if there is no leak.
Insufflation pressureQUICK, FIRM BUT GENTLE. Reduced mobility → EFFUSION or THICKENED MEMBRANE.
Referred ear painTMJ · TEETH · CERVICAL SPINE. Carried by CN V, VII, IX, X. Four sensory nerves to one small structure.
Ototoxic drugs to ask aboutAMINOGLYCOSIDES · ASPIRIN · NSAIDs · QUININE · FUROSEMIDE.
ACUTE otitis externaCanal SWOLLEN, NARROW, MOIST, PALE, TENDER; may be erythematous.
CHRONIC otitis externaCanal skin THICKENED, RED, ITCHY. Acute = PAIN, chronic = ITCH.
TM PERFORATIONCENTRAL = does NOT extend to the margin. MARGINAL = involves the margin. Usually secondary to OTITIS MEDIA; may drain through it.
TYMPANOSCLEROSISHYALINE DEPOSIT in the TM after severe otitis media or a healed perforation / tubes. USUALLY NOT CLINICALLY SIGNIFICANT.
SEROUS EFFUSIONAMBER fluid, sometimes BUBBLES. After URI or a change in ATMOSPHERIC PRESSURE.
OTITIS MEDIA on the drumRED · LANDMARKS LOST · BULGING. Purulent effusion. STREP PNEUMONIAE and H. INFLUENZAE.
Bulging is GRADEDNormal → mild → moderate → severe. The landmarks disappear as it progresses; that transition is what makes the effusion convincing.
BULLOUS MYRINGITISPAINFUL HEMORRHAGIC VESICLES on the TM and/or canal. MAY BE VIRAL OR BACTERIAL.
Know normal first“You have to see HUNDREDS of normal before you see anything abnormal … and then the abnormal will hit you in the face.”

Nose & Sinuses

TermWhat you need to know
TurbinatesSUPERIOR, MIDDLE, INFERIOR. The MAXILLARY SINUS DRAINS AT THE MIDDLE TURBINATE.
Why aggression matters up here“The roof of the mouth is the floor of your brain … anything that happened there CAN GO UP. Any infection in this area, you have to be a little more AGGRESSIVE.”
Recent DENTAL WORKCan affect the MAXILLARY SINUSES — the sinus floor sits directly above the upper tooth roots.
Nasal drug historyRHINITIS MEDICAMENTOSA (topical decongestants) and COCAINE. Neither is volunteered.
Epistaxis causesDIGITAL TRAUMA or other trauma · INFLAMMATION · DRY MUCOSA · FOREIGN BODY · TUMOR. RECURRENT, or WITH BLEEDING/BRUISING ELSEWHERE → SYSTEMIC problem.
Patency testOCCLUDE ONE NOSTRIL AND BREATHE IN. UNILATERAL obstruction → FOREIGN BODY, TUMOR, DEVIATED SEPTUM.
NASAL POLYP associationsALLERGIC RHINITIS · ASPIRIN SENSITIVITY · ASTHMA · CHRONIC SINUS INFECTION · CYSTIC FIBROSIS.
MUCOSA colorRED AND SWOLLEN → VIRAL rhinitis. PALE, BLUISH OR RED → ALLERGIC rhinitis.
PERFORATED septumTRAUMA · SURGERY · DRUG USE.
Sinus palpationPress UP on the FRONTAL sinuses AVOIDING THE EYES. Press UP on the MAXILLARY sinuses.
TransilluminationDARK ROOM. FRONTAL: light UP under the brow close to the nose. MAXILLARY: light DOWN just below the inner corner of the eye, MOUTH OPEN. No glow → thickened mucosa/secretions. NOT SENSITIVE OR SPECIFIC.
★ ACUTE SINUSITIS — three rules(1) Local tenderness, pain, fever, nasal discharge are SUGGESTIVE. (2) THE COLOR OF THE DISCHARGE IS NOT DIAGNOSTIC. (3) ACUTE BACTERIAL SINUSITIS IS UNLIKELY UNDER SEVEN DAYS — “it takes time to let it cook.”
★ SEPTAL HEMATOMAInjury disrupts vessels and PULLS THE LINING AWAY FROM THE CARTILAGE; blood collects between the two. URGENT DRAINAGE to prevent NECROSIS OF THE SEPTAL CARTILAGE — the cartilage has no blood supply of its own. “That blood HAS TO COME OUT.”
Don’t pull what you can’t nameA lesion everyone called a polyp turned out on imaging to be BRAIN TISSUE coming through. “You need to know what you’re looking at before you start pulling things.”

Oral Cavity & Centor

TermWhat you need to know
★ THE FOUR CENTOR CRITERIAFEVER (above 100.4°F / 38°C) · TONSILLAR EXUDATES or swelling · SWOLLEN AND TENDER ANTERIOR CERVICAL NODES · ABSENCE OF COUGH. Three PRESENT and one ABSENT — that is the half people misremember.
Why ABSENCE of coughA cough points TOWARD a viral cause, so its ABSENCE raises the probability of streptococcal infection.
★ MODIFIED CENTOR — THE AGE POINTS3–14 years: +1. 15–44 years: 0. 45 AND OLDER: MINUS 1. This lives ONLY inside the slide’s PICTURE — the slide text is one caption line.
Score → risk of strep pharyngitis≤0 → 1–2.5% · 1 → 5–10% · 2 → 11–17% · 3 → 28–35% · ≥4 → 51–53%.
Score → action≤0: NO further testing or antibiotics. Middle: THROAT CULTURE or RAPID ANTIGEN TEST. ≥4: CONSIDER EMPIRIC TREATMENT.
UVULA deviationFailure to rise WITH DEVIATION TO THE OPPOSITE SIDE → CN X PARALYSIS. The working side pulls unopposed, so the uvula points AWAY from the lesion.
TONGUE deviationASYMMETRIC PROTRUSION → CN XII LESION.
Tongue findingsSMOOTH, BEEFY RED → VITAMIN B12 DEFICIENCY. SORE AND SMOOTH → nutritional deficiency. GEOGRAPHIC TONGUE IS BENIGN.
TONGUE CANCER — where and whoLATERAL BORDER or UNDERSURFACE. INDURATED RED/WHITE lesions. MALES OVER 50.
Tongue palpationHold with GAUZE in one hand, palpate with the other, THEN SWITCH HANDS for the opposite side — the only way to reach both lateral borders.
DenturesTAKE THEM OUT and look UNDERNEATH for ulcers and lesions.
Lip findingsANGULAR CHEILITIS (corners) · ANGIOEDEMA · HERPES SIMPLEX.
TRENCH MOUTHNecrotising ulcerative gingivitis = VINCENT’S ANGINA. “You can SMELL them across the room.” Bacteria DESTROY TISSUE as they go. From POOR DENTAL HYGIENE and drug use.
TORUS PALATINUSBENIGN BONY GROWTH in the MIDLINE of the HARD PALATE. A normal variant, not a mass.
Hoarseness causesVIRAL LARYNGITIS · VOICE OVERUSE · LARYNGEAL NERVE DAMAGE · REFLUX · SMOKING.

Neck, Thyroid & Head

TermWhat you need to know
★ NODE CHAINS — in order, and NAME THEM ALOUDPREAURICULAR · POSTAURICULAR · OCCIPITAL · TONSILLAR · SUBMANDIBULAR · SUBMENTAL · SUPERFICIAL (ANTERIOR) CERVICAL · POSTERIOR CERVICAL · DEEP CERVICAL · SUPRACLAVICULAR. “I need to know WHERE YOU’RE PUTTING YOUR FINGER” — the practical is graded on naming as you touch.
Palpation techniquePADS of the INDEX and MIDDLE fingers.
NORMAL nodeROUND OR OVOID · SMOOTH · MOBILE · NON-TENDER.
TENDER nodeINFLAMMATION.
HARD or FIXED nodeMALIGNANCY. Tender and soft is reactive; hard and fixed is not.
★ LEFT SUPRACLAVICULAR nodeMETASTASIS FROM AN ABDOMINAL OR THORACIC MALIGNANCY. It drains territory far from the neck, so it redirects the whole search.
GENERALIZED lymphadenopathyHIV/AIDS · EPSTEIN-BARR VIRUS · LYMPHOMA · LEUKEMIA · SARCOIDOSIS.
★ LUDWIG’S ANGINASUBMANDIBULAR SWELLING AND ERYTHEMA = CELLULITIS OF THE FLOOR OF THE MOUTH. LIFE THREATENING — THE AIRWAY. Usually from LOWER TEETH. “It spreads FAST … you have to work with it QUICKLY.”
TRACHEAL deviationMASSES · ATELECTASIS · LARGE PNEUMOTHORAX.
Thyroid landmarkFind the CRICOID CARTILAGE first — it locates the isthmus and lobes.
THYROID — diffuse enlargement splits on TEXTURESOFT → GRAVES DISEASE. FIRM → HASHIMOTO THYROIDITIS. TENDER → THYROIDITIS.
Other thyroid findingsENDEMIC GOITER → IODINE DEFICIENCY. SINGLE NODULE → cyst or tumor. MULTINODULAR → metabolic process; RISK OF MALIGNANCY WITH FAMILY HISTORY.
HEADACHE patternsMIGRAINE and TENSION are EPISODIC. MIGRAINE and CLUSTER are UNILATERAL. Migraine is in BOTH lists, so read the two features together.
HEADACHE red flagsSUDDEN AND SEVERE → SUBARACHNOID HEMORRHAGE. NEW, PROGRESSIVE AND PERSISTENT → MASS. Also consider MENINGITIS.
HEAD examFINE HAIR → HYPERTHYROIDISM. COARSE HAIR → HYPOTHYROIDISM. Look for LICE, SEBORRHEIC DERMATITIS, PSORIASIS, ATYPICAL NAEVI, ACTINIC KERATOSIS. SIZE: ENLARGED → HYDROCEPHALUS or PAGET DISEASE; SMALL → MICROCEPHALY.