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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5230_Библиотеки_им_академика_М_И_Перельмана.pdf
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CoordinationFinger– nose, dysdiadochokinesia, tapping, heel– shin. Romberg’s This is tested with patient standing with eyes open then closed,
positive if more unbalanced with eyes closed; suggests sensory ataxia.
SensationPinprick, light touch, vibration, joint position; the spinal dermat-
omes of the front and back are shown in Fig.3.2. For spinal tract anatomy and function, see Table3. and Fig.3.3.
Fig.3.2 Dermatomes of the front (L)and back(R).
133NEUROLOGICAL
Fig.3.3 Cross- section of the spinal cord showing spinal tracts.
Table3. Spinal tracts and anatomy
Tract Modality Crosses (decussates) at
Lateral corticospinal (pyramidal) Motor Medulla
Anterior corticospinal Motor Level of exit of the cord
Posterior columns (dorsal) Light touch,
Spinothalamic Hard touch, pain,
vibration, position
temperature
Medulla
Level of entry to the cord
134 CHAPTER3 History and examination
Nerves ofthe handSee Table3.2 and Fig.3.4.
Table3.2 Innervation ofhand movements
Movement Nerve
Finger abduction and adduction Ulnar
Thumb opposition and abduction Median
Finger extension Radial
Fig.3.4 Sensation of thehand.
Gait This forms an essential and highly informative part of the examin-
ation of both the central and peripheral nervous systems; see Table3.3.
Table3.3 Gait examination
Gait Description Cause
Antalgic Painful gait, limping, short weight- bearing
Apraxic Unable to lift legs despite normal power,
Ataxic Uncoordinated, wide based, unsteady (as
Festinating A shuing gait with accelerating steps Parkinson’s
Hemiparetic Knee extended, hip circumducts and drags
Myopathic Waddling, leaning back, abdomen sticking
Shuing Short, shued steps, stooped, no arm
Spastic Restricted knee and hip movements, slow,
Steppage High steps with foot slapping, ‘foot drop’ Peripheral
on painful side
magnetic steps/ stuck to oor
if drunk), worse with eyes shut if sensory
leg; elbow may be exed up
out
swing
shuing, ‘wading through water’
Mechanical injury, sciatica
Hydrocephalus, frontal lesions
Cerebellar, sensory
Hemiplegia, eg CVA
Proximal myopathy
Parkinson’s
Pyramidal tract lesion, eg MS
neuropathy
Endocrine
History
Symptoms Weight loss, weight gain, appetite, sweating, heat/ cold intol-
erance, tremor, weakness, tiredness, dizziness, hirsutism, joint pain/ swelling, change in appearance (skin, hair, nails, face, eyes), change in clothes/ shoe/ hat size, altered sensation, ulcers, visual problems.
Cardiorespiratory features Chest pain, breathlessness, palpitations, sleep
apnoea.
GI/ urinary features Diarrhoea, constipation, nausea, vomiting, abdominal
pain, thirst, polyuria.
Reproductive features Menstrual irregularities, infertility, gynaecomastia,
galactorrhoea, impotence.
Psychiatric features Anxiety, mood changes, memory problems.
Eye featuresBlurred vision, visual eld defects, bulgingeyes.
Past medical historyHypercholesterolaemia (thyroid function aects lipid
levels), thyroid surgery, stroke, heart failure, liver failure, renal artery stenosis, renal failure, adrenal surgery, brain surgery.
Drug historySteroids, diuretics, OCP, HRT, levothyroxine, insulin.
Family historyDM, thyroid disease, pituitary tumours.
Examination (lying at45°)
General inspection Body habitus, ‘bualo hump’, facial appearance
(‘moon face’), striae, bruising, muscle wasting, hyperpigmentation, coarse skin, prominent jaw and brow ridge, goitre, gynaecomastia, hir­sutism, acanthosis nigricans, vitiligo, acne, necrobiosis lipoidica, pre- tibial myxoedema.
Hands Temperature, sweating, size, tremor.
Eyes Lid lag, proptosis, exophthalmos, bitemporal hemianopia, cranial
nerve III, IV, or VI palsy, fundoscopy.
NeckGoitre, thyroidlumps. Cardiorespiratory idHR, idBP, postural hypotension, irregular pulse, per-
ipheral oedema, bibasal crackles(LVF).
Neurological Cranial nerve III/ IV/ VI palsy, peripheral neuropathy, slow
relaxing reexes, weakness (myopathy).
Other Joints, skin, genitalia, fundoscopy, urine analysis, U+E, early
morning cortisol, TFTs, short Synacthen specialist tests on advice from an endocrinologist.
®
test (E p. 599), GTT— more
135ENDOCRINE
136 CHAPTER3 History and examination
Skin
History
Presenting skin complaint TimingHow long present for, sudden or gradual
onset, getting better orworse; sites aected; bleeding, weeping; light (seasonal variability), pet dander, night- time, water;
torsEmollient cream, topical/ systemic steroids.
Current health Anorexia, diarrhoea, fever, headache, fatigue, weight loss,
depression, sore throat, jointpain.
Past medical history Previous skin disease, DM, IBD, asthma/ atopy, vari-
cose veins, peripheral arterial disease, cardiac problems, endocrine disease, coeliac disease, neurological problems, ulcers, trauma, sarcoid, porphyria, SLE, malignancy, sensitivity of skin to sun exposure, lifelong history of sun exposure or use of sunbeds.
Drug history Dermatological agents being used at present and their ef-
fects, previous drugs used and their eects, oral and topical steroids, other drugs being taken, immunosuppressants, drug allergies.
AllergyHayfever, pet dander, dust mite,etc.
Occupational historyCurrent and previous jobs and eect of work upon
skin, exposure to chemicals; hobbies and recreational activities.
Family history Anyone else in the family aected; need to dierentiate
inherited pathology versus infectious pathology.
Travel historyRecent foreign travel and relationship of any travel to skin
disease— vaccinations/ prophylaxis taken for foreign travel.
FunctionRestricted actions, eect on life, mobility, occupation, dominant
hand, hobbies/ sports, smoking, social support.
Symptoms Itch (localized or generalized), pain, burning,
Exacerbating factorsDietary components, drugs, sun-
Examination
The whole body should be examined in good natural light; patients com­plaining of a rash on their arm may well have other tell- tale signs else­where on the body. Ask patients to fully undress to enable a full skin inspection. Remember the importance of gaining consent and having a chaperone present.
Distribution Solitary lesion, exor aspects of limbs/ trunk, extensor
aspects of limbs/ trunk, scalp/ eyebrows/ gutters of nose, sun- exposed sites, tip of nose, helix of ear, webspaces of hands or feet, periumbilical.
Morphology Noting or describing the appearance of the rash using the
terms dened in Boxes 3.4– 3.7 renes the list of dierential diagnoses.
Hair Alopecia (hair loss) may be generalized or localized and scarring/
non-scarring. Hirsutism (hair in the typical male distribution), hypertrichosis (excessive hair growth).
NailsClubbing, pitting, ridging, onycholysis, nail loss, thinning of nail plate,
discolouration.
Location Original site and subsequent
Relieving fac-
K Box 3.4 Non- palpable skin lesions
EcchymosisBruising; discolouration from blood leaking into theskin.
MaculeFlat, well- dened area of altered skin pigmentation.
PetechiaNon- blanching, pinpoint- sized purple macule.
Purpura Purple lesion resulting from free red blood cells in the skin,
non- blanching.
Telangiectasia Abnormal visible dilatation of blood vessels (spider naevi).
K Box 3.5 Palpable skin lesions
NoduleSolid, mostly subcutaneous lesion (>0.5cm diameter).
PapuleRaised, well- dened lesion (<0.5cm diameter).
PlaqueRaised, at- topped lesion (usually >2cm diameter).
Weal Transient, raised lesion with pink margin.
UrticariaWeals with pale centres and well- dened pink margins.
K Box 3.6 Blisters
AbscessFluctuant swelling containing pus beneath the epidermis.
BullaFluid- lled blister larger than a vesicle (>0.5cm diameter).
PustuleWell- dened pus- lled lesion.
VesicleFluid- lled blister (<0.5cm diameter).
K Box 3.7 Skin defects
AbrasionScraping o supercial layers of the skin (a graze).
Atrophy Thinning and loss of skin substance.
CrustDried brownish/ yellow exudates.
ErosionSupercial break in the continuity of the epidermis.
ExcoriationLinear break in the skin surface (a scratch).
FissureCrack, often through keratin.
Incisional woundBreak to the skin by sharp object.
LacerationBreak to the skin caused by blunt trauma/ tearing injury.
LichenicationSkin thickening with exaggerated skin markings.
ScaleFragment of dryskin.
UlcerLoss of epidermis and dermis resulting inscar.
137SKIN
138 CHAPTER3 History and examination
Oncological/ haematological
History
Symptoms Weight loss, anorexia, weakness, lethargy, fatigue, cough,
haemoptysis, shortness of breath, postural dizziness, nausea, vomiting, diarrhoea, constipation, PR bleeding, lumps, swelling, pain, frac­tures, bone pain, polyuria, prostatism, bruising, recurrent epistaxis, haemarthrosis, heavy menstrual loss, recurrent miscarriage, recurrent VTE, fevers, infections, focal neurology.
Past medical history DM, asthma, iBP, IHD, liver disease, jaundice, thy-
roid problems, anaemia, malignancy (and radiotherapy), epilepsy, gastric or small bowel surgery, malabsorption, chronic disease (eg RA), blood transfusions, splenectomy.
Drug history Chemotherapy (regimen, date of last dose, response, side
eects), iron, vitamin B post- splenectomy, long- term antibiotics, OCP, allergies.
Social historySmoking, alcohol, family support, living circumstances, home
help, occupation, previous exposure to dyes/ asbestos/ coal tar, racial origin, diet (vegan, vegetarian), recreational druguse.
Family history Malignancy, thalassaemia, sickle- cell anaemia, haemo-
philia, von Willebrand’s disease, pernicious anaemia, spherocytosis, thrombophilia.
Examination
General inspection Bruising, pigmentation, rashes and nodules,
ulceration, cyanosis, plethora, jaundice, excoriations, racial origin (haemoglobinopathies and thalassaemias).
Hands Nails (koilonychias, pallor, clubbing), palmar crease pallor,
arthropathy.
FaceEyes (jaundice, pallor), mouth (gum hypertrophy or bleeding, ulcer-
ation, candida, atrophic glossitis, angular stomatitis, gingivitis).
Lymph nodesCervical, axillary, epitrochlear (elbow), inguinal.
BonesBony pain in sternum, spine, clavicles, scapulae.
AbdomenHepatomegaly, splenomegaly, para- aortic nodes, ascites.
LegsVasculitis, bruising, pigmentation, ulceration, neurologicalsigns.
OtherFundi (haemorrhages, engorged veins, papilloedema), temperature
chart, urinalysis.
/ folate, aspirin, anticoagulants, vaccinations
2
Breast (male and female)
(a)
Supraclavicular
11% lo
quadrant
(b)
History
LumpSize, duration, mobility, pain, nipple discharge/ bleeding/ inversion,
skin changes, previous breastlumps.
Past obs/ gynae history Number of pregnancies, age of rst pregnancy,
breastfeeding, menarche, menopause.
Past medical history DM, asthma, iBP, IHD, clotting problems, liver
disease, anaemia, previous malignancy, epilepsy.
Family historyBreast cancer (male/ female), gynae cancer— age of relative
at their diagnosis.
Drug historyHRT, COCuse.
Examination (lying at45°)
Ensure a chaperone is present and document their details in the notes (name, job title). Examine both breasts (normal side rst):
Inspection Asymmetry, scars, skin changes, nipple discharge/ inversion,
skin tethering, erythema, oedema. Ask the patient to tense pectoral wall by putting their hands on hips and tensing. Ask the patient to lean forward. Look for any skin tethering.
Palpation Ask the patient to show you where the lump is, palpate all four
quadrants (Fig.3.5) and axillary tail, assess any palpable masses.
Lymphadenopathy Axilla, cervical, supraclavicular. The patient must be
fully relaxed for you to adequately palpate the axillary nodes. Take the weight of their arm in yours as you palpate.
OtherLiver,spine.
139BREAST (MALE AND FEMALE)
lymph nodes
50% upper
outer
quadrant
wer
outer
Fig.3.5 Anatomy of the breast. (a)Quadrants of the breast showing proportion of breast cancer by location. (b)Glands and lymphatics of the right breast.
15% upper inner quadrant
18% nipple
6% lower inner quadrant
Axillary
lymph nodes
140 CHAPTER3 History and examination
er
Pupil
Eyes
History
Symptoms Reduced/ impaired vision or visual loss, red eye, discomfort
(gritty or FB sensation), pain of the eye or soft tissues around the eye, dry eyes or excessive watering, itch, swelling, photophobia or haloes around lights, oaters or ashing lights, diplopia, discharge.
Past ophthalmic history Glaucoma, myopia, cataracts, previous surgery,
glasses/ contact lens prescription and last optometry check- up.
Past medical history Numerous systemic diseases can aect the eye,
including DM, iBP, vascular disease, RA, SLE, thyroid disease,MS.
Drug history Ophthalmic medications, steroids, anticholinergics, medica-
tions for coexisting disease; allergies.
Family historyGlaucoma, retinoblastoma, retinitis pigmentosa.
Social history Ability to self- care, impact eye disease has upon ADLs and
home support received/ needed, driving.
Upper eye lid
Limbus
Conjunctiva ov sclera
Lateral canthus
Lower eye lid
Fig.3.6 Surface anatomy of the righteye.
Examination
InspectionExophthalmos, proptosis, jaundice, pallor, xanthelasma, eyelids
(cysts, inammation), red eye, corneal arcus, periorbital cellulitis (Fig.3.6).
Visual acuity This must be tested in all patients:
• Use a Snellen chart at 6m to test visualacuity
• Make sure the patient is using the correct glasses for the test (reading vs
distance); if in doubt, use a pin- hole in a piece ofcard
• If visual acuity is very bad, assess ability to count ngers, awareness of
movement (waving hand), or perception of light (pen torch).
Pupillary response and reexes Check the pupils are equal, reacting to light
and accommodation (PERLA) and for a relative aerent papillary defect. Look for the red reex (absent in dense cataracts). An absent red reex at the 6wk baby check is a red ag (treat this as a same- day urgent referral).
Visual elds Confrontation testing to identify any visual eld loss and to
establish if the defect is unilateral or bilateral (Ep. 31).
Ocular movementsLook for diplopia, loss of conjugate gaze, or nystagmus.
Medial canthus
Iris with lens beneath
Ophthalmoscopy
• With the ophthalmoscope set on +0 the cornea and anterior chambers
can be examined.  or 2 drops of uorescein highlights corneal ulcers, abrasions, and foreign bodies, especially under the bluelight
• With the ophthalmoscope set on 0 the user can visualize the retina. It
is important to dilate the pupil with  or 2 drops of a weak mydriatic (Box 3.8) (eg 0.5% or % tropicamide) to allow full visualization of the retina. The risk of causing acute glaucoma with mydriatics issmall.
K Box 3.8 Descriptive terms inophthalmology
Accommodation Alteration in lens and pupil to focus on near/ far objects.
Acuity Ability of the eye to discriminate ne detail.
Anterior chamberBetween cornea and iris, containing aqueous.
AqueousFluid- like jelly in the anterior chamber of theeye.
BlepharitisInammation/ infection of eyelids.
CanthusMedial or lateral junction of the upper and lower eyelids.
ChemosisConjunctival oedema.
ChoroidLayer sandwiched between retina and sclera.
ConjunctivaMucous membrane covering sclera and cornea anteriorly.
CycloplegiaCiliary muscle paralysis preventing accommodation.
DacryocystitisInammation of the lacrimalsac.
EctropionEyelids evert outwards (away from the cornea).
EntropionEyelids invert towards the cornea (lashes irritate cornea).
FoveaHighly cone- rich area of the macula (yellow- spot).
Fundus Area of the retina visible with the ophthalmoscope.
HyphaemaBlood in the anterior chamber seen as a red uidlevel.
HypopyonPus in the anterior chamber seen as a white uidlevel.
LimbusBorder between cornea and sclera.
MaculaRim around the fovea, rich in conecells.
Miotic Agent resulting in pupillary constriction (eg pilocarpine).
Mydriatic Agent resulting in pupillary dilatation (eg tropicamide).
Optic cupDepression in the centre of the opticdisc.
Optic discOptic nerve head seen as white opacity on fundoscopy.
Posterior chamberChamber between the iris and lens.
Presbyopia Age- related reduction in near acuity (long- sightedness).
PtosisDrooping eyelid(s).
Sclera The visible white brous layer of theeye.
ScotomaDefect resulting in loss of a specic area of vision.
StrabismusSquint, loss of conjugate gaze.
Tonometer Apparatus for indirectly measuring intraocular pressure.
VitreousJelly- like matter which occupies the globe behind thelens.
141EYES
142 CHAPTER3 History and examination
Head andneck
History
As well as a good general history, specic symptoms to note include:
Ears Pain, blocked ears, wax, discharge, tinnitus, deafness, unilateral/
bilateral features, vertigo, trauma, itching, FBs, noise exposure, occupation.
NoseBlocked nose, watery discharge, sneezing, itching, coughing, change
in voice, altered sensation of smell/ taste, external deformity/ recent trauma, epistaxis, sinusitis; ask about daytime variation in symptom severity, pattern of obstruction, eects on speech and sleep. Are symp­toms uni/ bilateral?
ThroatDysphagia, pain on swallowing, hoarseness, diculty opening jaw
(trismus), stridor, sleep apnoea/ snoring; ask about neck lumps, vomiting, heartburn, waterbrash (acid regurgitation or lling of mouth with saliva).
Examination
Ears Inspect The pinna, auditory meatus, tenderness over pinna or
mastoid; (colour, bulging/ retraction, perforation, exudate); lowing ‘Hearing tests’text.
Nose Look for Obvious scars, deviations/ deformities, tilt the head back
and look down each nostril (Fig.3.8); spray rst), look for polyps, inamed turbinates,pus.
Throat Inspect The lips, around and inside themouth; Examine The tongue
and tonsils using a torch and tongue depressor, check palate movements by asking the patient to say ‘ah’ (Fig.3.9).
Neck Look for Swellings, asymmetry,scars; Ask The patient to swallow,
protrude the tongue; to take a sip of water; tenderness;
Otoscopy Examine all four quadrants of the eardrum (Fig.3.7)
Test hearing See fol-
Rhinoscopy (Administer lidocaine
Palpate The neck from behind and ask the patient
Feel for Tracheal deviation, lymphadenopathy,
AuscultateFor abruit; Examine Any lumps (Epp. 472–3).
Hearing tests(E OHCS11p. 390.)
WhisperWhisper a dierent number into each ear, standing 30cm away
while blocking the other ear. Ask the patient to repeat it inturn.
Tuning forktests
Rinne’s testPlace the tuning fork on the patient’s mastoid bone until it is
no longer heard; then place the fork near the external auditory meatus where it is still heard in a normal ear, but not in an ear with conductive deafness. Normally air conduction > bone conduction. Confusingly, a normal result is called Rinne positive.
Weber’s testPlace the tuning fork in the middle of the forehead and ask
which side the sound is loudest; in sensorineural deafness the sound is loudest in the normal ear, in conductive deafness the sound is loudest in the abnormalear.