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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3230_Библиотеки_им_академика_М_И_Перельмана
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CHAPTER 5 General examination physical signs
82
Neck stiffness
Distinguish between limited range of neck movement and neck stiffness
throughout range of movement.
- Limited neck range of movement
Some differential diagnoses and typical outline evidence
Chronic
cervical
spondylitis with
osteophytes
Suggested by: no fever or associated symptoms
Confirmed by: limitation in range of neck movement but
no stiffness within free range of movement. Normal
WBC, no fever, no neurological signs, X-ray appearance
of neck
- Neck stiffness throughout range of movement
Bacterial
meningitis
Suggested by: gradual headache over days, photophobia,
vomiting. Fever, high neutrophil count. Petechial rash in
meningococcal meningitis
Confirmed by: lumbar puncture: turbid cerebrospinal
fluid (CSF). iCSF neutrophil count with d glucose.
Bacteria on microscopy. Growth of bacteria on culture
of CSF
Viral meningitis Suggested by: gradual headache over days. Fever, high
lymphocyte count, normal neutrophil count
Confirmed by: lumbar puncture: clear CSF. iCSF
lymphocyte count with normal glucose. No bacteria
on microscopy. No growth of bacteria on CSF culture
Meningismus
due to viral
infection
Suggested by: gradual headache over days. Fever, high
lymphocyte count, normal neutrophil count
Confirmed by: lumbar puncture: clear CSF. Normal CSF
white cell count. No bacteria on microscopy. No growth
of bacteria on CSF culture
Subarachnoid
hemorrhage
Suggested by: sudden onset of headache over seconds.
Variable degree of consciousness. No fever. Normal
white cell count
Confirmed by: CT or magnetic resonance imaging (MRI)
brain scan. Lumbar puncture: blood-stained CSF that
does not clear in successive bottle collection, or
presence of xanthochromia in CSF (12 hours to
2 weeks after hemorrhage)

NECK STIFFNESS1
83
Acute cervical
spondylitis
Suggested by: gradual neck pain (occasionally a
headache) over hours or days. Immobile neck.
Usually past history of similar episodes. No fever
Confirmed by: above history
Posterior fossa
tumor
Suggested by: headache, papilledema
Confirmed by: CT or MRI scan appearances
Anxiety with
semi-voluntary
resistance
Suggested by: improvement with reassurance or
temporary distraction
Confirmed by: resolution after rest and observation
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CHAPTER 5 General examination physical signs
84
Hair loss in a specific area
Examine overall and then gently part hair to examine the scalp. Use a
magnifying glass if hair is abnormal.
Some differential diagnoses and typical outline evidence
Alopecia areata Suggested by: well-circumscribed loss with
exclamation-mark hairs
Confirmed by: above clinical appearance
Alopecia totalis Suggested by: total hair loss on head and body
Confirmed by: above clinical appearance
Polycystic
ovary
syndrome
Suggested by: bitemporal recession and occipital thin-
ning. Hirsutism on trunk. Onset near puberty. Obesity
Confirmed by: i testosterone and dSHBG (sex
hormone-binding globulin). iLH (luteinizing hormone)
,
ovarian ultrasound
Testosterone-
secreting
ovarian tumor
Suggested by: bitemporal recession and occipital
thinning. Rapid onset over months
Confirmed by: ii testosterone and dLH
, ovarian
ultrasound scan and laparoscopy

DIFFUSE HAIR LOSS1
85
Diffuse hair loss
Examine trunk, pubic, and limb hair too.
Some differential diagnoses and typical outline evidence
Cytotoxic
drugs
Suggested by: mainly head hair loss. History of recent
cytotoxic drugs
Confirmed by: improvement after stopping cytotoxic
drug
Iron deficiency Suggested by: mainly head hair loss. Koilonychia, pallor
of conjunctive
Confirmed by: dHb, dMCV (mean corpuscular volume),
dMCHC (mean corpuscular hemoglobin concentration),
d ferritin
Severe illness Suggested by: mainly head hair loss. History of recent
severe illness
Confirmed by: improvement with restoration of health
Hypogonadism Suggested by: loss of hair from axilla, pubic area
Confirmed by: testosterone d or estrogen d with FSH i
and iLH in primary gonadal failure; dLH or normal,
dFSH or normal in secondary hypogonadism
Recent
pregnancy
Suggested by: mainly head hair loss. Recent pregnancy
Confirmed by: improvement after delivery
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CHAPTER 5 General examination physical signs
86
External ear abnormalities
Inspect the pinna for scars and other abnormalities. Examine the auditory
meatus by first pulling the pinna up and back to straighten the cartilagi-
nous bend. (In infants, the pinna is pulled back and down.) Swab any
discharge, and remove any wax.
Some differential diagnoses and typical outline evidence
Congenital
anomalies
Suggested by: accessory tags, auricles and preauricular
pit, sinus, or fistula and atresia
Confirmed by: above clinical appearances
Infected
preauricular
sinus
Suggested by: looking like infected sebaceous cyst
Confirmed by: deep tract that lies close to the facial
nerve
Chondroderma-
titis nodularis
chronica helicis
Suggested by: painful nodular lesions on the upper
margin of the pinna in men
Confirmed by: excision of skin and underlying cartilage
Pinna
hematoma
resulting in a
“cauliflower” ear
Suggested by: history of blunt trauma
Confirmed by: appearance of bleeding in the
subperichondrial plane that elevates the perichondrium
to form a hematoma
Exostosis
(localized bony
hypertrophy)
may cause
build-up of
wax or debris
or conductive
deafness
Confirmed by: smooth, often multiple (bilateral)
swellings of the bony ear canals
Wax
(cerumen) may
cause conductive
deafness if it
impacts
Suggested by: dark brown, shiny, soft mass
Confirmed by: improvement in hearing after removal
Foreign bodies
in the ear
Suggested by: visible foreign body and inflammation
(in child or learning-disabled patient)
Confirmed by: retrieval of foreign body

PAINFUL EAR1
87
Painful ear
Consider referred pain from the neck (C3, C4, and C5), throat, and teeth
and examine these as well. Insert the largest comfortable aural speculum
gently.
Some differential diagnoses and typical outline evidence
Otitis externa
(swimmer’s ear)
due to eczema,
psoriasis, trauma,
Pseudomonas,
fungal infection
Suggested by: pain, discharge, and tragal tenderness
Confirmed by: acute inflammation of the skin of the
meatus, culture of swab
Malignant
necrotizing
otitis externa
Suggested by: pain, discharge, and tragal tenderness in a
diabetic, elderly, or immunosuppressed person, facial
palsy
Confirmed by: X-ray showing local bone erosion,
nuclear bone scan, and tagged white cell scan
Furunculosis
(staphylococcal
abscess in hair
follicle) often
diabetic
Suggested by: acutely painful throbbing ear
Confirmed by: appearance of a boil in the meatus
Bullous
myringitis
(associated with
influenza
infection or
Mycoplasma
pneumoniae)
Suggested by: extremely painful hemorrhagic blisters
on the drum and deep meatal skin, and fluid behind
the drum
Confirmed by: above clinical appearance
Barotrauma
(aerotitis)
Suggested by: history of ear pain during descent in an
aircraft or in diving
Confirmed by: relief by decompression (e.g., holding
nose and swallowing)
Temporo-
mandibular
joint
dysfunction
Suggested by: earache, facial pain, and joint clicking or
popping related to malocclusion, teeth-grinding or joint
derangement, and stress
Confirmed by: tenderness exacerbated by lateral
movement of the open jaw, or trigger points in the
pterygoids
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CHAPTER 5 General examination physical signs
88
Ear discharge
Examine the eardrum quadrants in turn. Note color, translucency, and
any bulging or retraction of the membrane. Note size, position, and site
(marginal or central) of any perforations. Drum movement during a
Valsalva maneuver also depends on a patient’s Eustachian tube.
Some differential diagnoses and typical outline evidence
Acute otitis
media
(due to
pneumococcus,
hemophilus,
streptococcus,
and staphylo-
coccus,
occasionally
complicated by
mastoiditis)
Suggested by: rapid onset over hours of pain and fever,
irritability, anorexia, or vomiting after viral upper respi-
ratory tract infection
Confirmed by: bulging red drum or profuse purulent
discharge for 48 hours after drum perforates
Otitis media
with effusion
(serous, secre-
tory, or glue ear)
usually in young
children
Suggested by: gradual onset over weeks or months of
deafness and intermittent ear pain
Confirmed by: loss of drum’s light reflex or retraction
relieved by grommets
Chronic
suppurative
otitis media
(may be
associated with
cholesteatoma,
petrositis,
labyrinthitis;
facial palsy;
meningitis;
intracranial
abscess)
Suggested by: purulent discharge, hearing loss, but no
pain
Confirmed by: central drum perforation
Cholesteatoma
(locally destruc-
tive stratified
squamous
epithelium)
Suggested by: foul discharge, deafness, headache, ear
pain, facial paralysis, and vertigo
Confirmed by: continuing mucopurulent discharge,
pearly white soft matter (keratin) in attic or posterior
marginal perforation

EAR DISCHARGE1
89
Chronic otitis
externa
Suggested by: watery discharge, itching
Confirmed by: erythema and weeping of meatus
Auditory canal
trauma
Suggested by: bloody discharge
Confirmed by: history of trauma, laceration, and
erythema
CSF otorrhea Suggested by: history of head or facial trauma or
surgery
Confirmed by: halo sign on filter paper
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CHAPTER 5 General examination physical signs
90
Striking facial appearance
This is best recognized when meeting the patient for the first time, but
there is a wide normal variation.
Some differential diagnoses and typical outline evidence
Parkinson’s
disease
Suggested by: mask-like (akinetic) face ± hand or
head tremor
Confirmed by: response to dopaminergic drugs
Chorea
(Huntington’s
chorea or drug
effect)
Suggested by: choreiform—jerky, purposeless
facial movement or athetosis (writhing facial
movement)
Confirmed by: Family history, or response to withdrawal
of drug or dose reduction (if due to drug effect)
Bilateral upper
motor neuron
lesion
(due to
amyotrophic
lateral sclerosis,
cerebrovascular
disease, myas-
thenia gravis)
Suggested by: paucity of movement of face
Confirmed by: other features of cause and MRI or
CT scan
Thyrotoxicosis Suggested by: anxious looking with lid retraction and lag
Confirmed by: dTSH and iT3 or iT4
or both
Hypothyroidism Suggested by: puffy face, obesity, cold intolerance,
tiredness, constipation, bradycardia
Confirmed by: iTSH, dFT4
Acromegaly Suggested by: large, wide face, embossed forehead,
jutting jaw (prognathism), widely spaced teeth and
large tongue
Confirmed by: insulin-like growth factor (IGF) i. Failure
to suppress growth hormone (GH) to <2 mU/L with
oral GTT. Skull X-ray confirms bony abnormalities.
Hand X-ray shows typical tufts on terminal phalanges.
MRI or CT scan showing enlarged pituitary fossa

STRIKING FACIAL APPEARANCE1
91
Cushing’s
syndrome
pituitary-driven
Cushing’s
disease, or
autonomous
adrenal
Cushing’s, or
glucocorticoid
therapy
Suggested by: round, florid face (and trunk with purple
striae) with thin arms, legs, and hirsutism. Inability to
rise from squatting position (due to proximal
myopathy)
Confirmed by: midnight cortisol i and/or failure
to suppress on dexamethasone, or drug history of
glucocorticoids
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