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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4440_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Foreword
- •Preface
- •Acknowledgement
- •Contents
- •1.1 General History Taking and Examination
- •1.2.2 Systemic Examination
- •3.2 Examination of Ear
- •6.2.2 Oral Cavity Examination
- •7.1.2 Odynophagia (Painful Swallowing)
- •7.1.5 Cough
- •7.1.1 Throat Pain
- •7.1.6 Expectoration
- •7.1.7 Halitosis
- •7.1.9 Swelling/Bulging/Growth
- •7.1.10 Snoring
- •7.2.3 Other Examination Includes
- •10.3.1 Swelling or Growth or Ulcer
- •10.4.3 Nasopharynx
- •10.4.4 Oropharynx
- •10.4.5 Laryngeal Tumours
- •10.4.6 Laryngopharyngeal Tumours
- •10.4.7 Oesophageal Tumour
- •10.4.8 Salivary Gland Tumours
- •10.4.15 Lymphoma
- •10.5.1 Neck Sweeling/Lump/Mass
- •10.5.2 Sinus
- •10.5.3 Head Movement
- •10.5.4 Neck Pain
- •13.1 Maxillofacial/Facial Trauma
- •13.1.1 Overview of Maxillofacial Fracture
- •15.1 Facial Aesthetic, Structural and Functional Deformities
- •16.1 Craniofacial Anomalies
- •17.1 Skull Base
- •18.1.3 Stridor
- •18.1.4 Wheeze
- •18.1.5 Stertor
- •18.2.1 Acute Dysphagia
- •18.3.4 Oral Bleeding

2.3 Symptomatology ofEar, Nose andThroat (ENT) andHead andNeck Surgery Diseases
2.3 Symptomatology ofEar,
Nose andThroat (ENT)
andHead andNeck Surgery
Diseases (Table 2.3)
Table 2.3 Symptomatology of ENT and head and neck diseases
Symptoms of ear
diseases
Ear discharge
Hearing loss
Pain
Tinnitus
Vertigo
Injury
Facial palsy
Deformity
Foreign body
Swelling
Bleeding
Vesicle
Itching
Blockage
Heaviness
Headache
Fever
Nose/paranasal sinus
diseases Oral cavity diseases Oropharynx
Nasal obstruction
Rhinorrhoea
Epistaxis
Deformity
Facial pain
Swelling
Decreased or loss of
smell
Foul smell
Bleeding
H/o foreign body
Itching nose
Nasal/palate mass
Postnasal drip
Numbness on face
Pus discharging from
nose
Loosening or
numbness of teeth
Watering of eye
Loss or change in
vision
Trismus
Headache
Pain
Halitosis
Loose denture
Discharge
Swelling/growth
Deformity
Injury
Trismus
Ulcer
Ankyloglossia
Altered salivation
Altered taste
Discoloration of
mucosa
Lump in cheek
Difculty in chewing
Numbness of tongue
or mouth
Swelling of jaw
Ill-tting denture
Oral ulcer
Pain in throat
Dysphagia
Odynophagia
Postnasal drip
F B sensation
change of voice
stridor
swelling/growth
Ulcer in oropharynx
H/o FB ingestion
Cough
Dyspnoea
Trismus
Pain aggravated on
swallowing
67
Head and neck
diseases
Swelling/lump
Pain
Stridor
Injury
Change of voice
Dysphagia
Restricted neck
movement
Pain while
movement of neck
Odynophagia

68
2 Local Examination ofORL: Head andNeck Surgery
2.4 Symptomatology ofENT
andHead andNeck Disease
(Table2.4)
Table 2.4 Symptoms of thyroid disease, anterior skull base diseases, and maxillofacial and middle skull base
diseases
Thyroid disease/parathyroid
disease or tumours
Neck swelling
Increased weight despite
decreased appetite
Weight loss despite
increased appetite
Diarrhoea/constipation
Loss of temporal hair
Altered menstruation
Dry skin
Heat/cold intolerance
Dysphagia
Respiratory distress
Hoarseness of voice
Anterior skull
base
Loss of vision
Nasal mass
Headache
Altered sense of
smell
Swallowing
problem
Change of voice
Maxillofacial trauma/
orthognathic
Trismus
Pain
Swelling
Decrease in or loss of
vision
Bleeding nasal or oral
Facial deformity
Occlusal deformity
Loss of teeth
Anophthalmos
H/o trauma +
Dental occlusal
deformities
Facial deformity
Lengthening of face
Middle skull base (sellar, parasellar,
etc.)
Headaches
Vision problems
Unexplained tiredness
Mood changes
Irritability
Changes in menstrual cycles
Erectile dysfunction
Infertility
Inappropriate breast growth/
production of breast milk
Cushing’s syndrome
Weight gain
Bruising easily
Irritability, anxiety, depression
Dizziness
Confusion
Flushing of face
Weak muscles
Irregular heartbeat
Acromegaly
Lowered sex drive
Impotency
Loss of body hair
Abnormal sexual development and
growth in children

2.5 Symptomatology ofENT andHead andNeck Diseases
69
2.5 Symptomatology ofENT
andHead andNeck Diseases
(Table2.5)
Table 2.5 Symptoms of head and neck oncology, salivary gland diseases, trachea and bronchus, lateral skull base
disease and nasopharynx
Trachea and
Head and neck oncology Salivary gland diseases
Nasal mass/swelling/
growth
Loss of smell
Neck swelling
Oral ulcer/growth/swelling
Dysphagia
Odynophagia
Ear pain
Hoarseness of voice
Haemoptysis
Lump in neck
Persist nasal obstruction
Nose bleed
Double vision
Persistent hoarse voice
Persistent numbness or
weakness
Difculty breathing
Referred ear pain
Halitosis
Loosening of teeth
Unexplained weight loss
Fatigue
Jaw pain
Swelling in neck,
retromandibular area, oral
cavity, submandibular
area
Dry mouth
Hypersecretion of saliva
Facial nerve weakness
Numbness over face
Odynophagia
Trismus
Pain and swelling in
gland area while having
meal
bronchus Lateral skull base Nasopharynx
Dyspnoea
Cough
Haemoptysis
Stridor
Wheezing
Shortness of
breadth
Pneumonia
Fever
Chest discomfort
Fatigue
Difculty talking
on phone
U/L hearing loss
Vertigo
Tinnitus
Symptoms of facial
nerve paralysis
Headache
Tiredness
Gait dysfunction
Nasal
obstruction
Epistaxis
Palatal bulge
Headache
Hearing loss
Blood in
saliva
Mouth
breather
Diplopia
Cheek
swelling
Lump in neck

70
2 Local Examination ofORL: Head andNeck Surgery
2.6 Symptomatology ofENT
andHead andNeck Diseases
(Table2.6)
Table 2.6 Symptomatology of laryngeal disorders, hypopharyngeal disorder, oesophageal disorder, facial cosmetic
and facial plastic surgery and craniofacial disorders
Larynx Laryngopharynx Oesophagus
Hoarseness of voice
Breathy voice
Loss of vocal pitch
Inability to speak loudly
Dysphonia
Dyspnoea
Stridor
Throat pain Neck pain
Odynophagia
Tingling sensation in throat
Dry cough
Cough after eating or lying
down
Choking or coughing while
swallowing
Throat clearing
Dry throat
Irritation in throat
Dysphagia
Odynophagia
Hoarseness of voice
Throat pain
Regurgitation of
food
Burning sensation in
throat
Lump in neck
Ear pain
Dysphagia
Odynophagia
Burning
sensation
Cough
Weight loss
Vomiting
Chest pain
Haematemesis
Difcult
breathing
Dry mouth
H/o aspiration
Facial cosmetic/
aesthetic surgery
Loss of hair
Thinning of hair
Wrinkle on face
Double chin
Spot of face
Growth/swelling/ulcer
Unwanted hair
Deviated nose
Deviated face
Twisted nose
Thickening of skin of
nose
Craniofacial
deformities
Swelling
Cleft lip
deformities
Non-cleft lip
deformity
Cleft palate
deformity
Triple nose
Absence of nose
Difculty in
breathing
Small jaw

2.7 Red Flag Symptoms oftheHead andNeck
2.7 Red Flag Symptoms
oftheHead andNeck
(Table2.7)
Table 2.7 Red ag symptoms of head and neck
Location Clinical features Possible diagnosis
Head Nuchal rigidity/reduced range of movement Meningitis
Face Loss of cranial nerve functions Cranial nerve palsy
Ischaemic stroke
Eye Ptosis
Incomplete lid closure
Xanthelasma
Exophthalmos
Yellow sclera
Conjunctival injection
Conjunctival pallor
Horner syndrome
Mouth Angular cheilitis
Tonsillar erythema
Strawberry tongue
Vesicle, blister
Coated tongue
6th cranial nerve palsy
Ischaemic stroke
Hyperlipidemia
Graves’ disease
Jaundice
Conjunctivitis
Anaemia
Arterial dissection, tumour
Iron deciency
Acute tonsillitis
Scarlet fever
Herpes viral infection
Leucoplakia, candidiasis
71

72
2 Local Examination ofORL: Head andNeck Surgery
2.8 Signs ofENT andHead
andNeck Surgery Diseases
(Table2.8)
Table 2.8 Signs of ENT and head and neck with their denition
Sign Denition Diagnosis
Omega sign Infantile omega-shaped epiglottis Laryngomalacia
Phelp’s sign Loss of crest of bone (caroticojugular crest)
between carotid canal and jugular bulb—a CT
nding
Schwartz sign
(amingo ush sign)
Rising sun sign in ear Red vascular hue seen behind TM High jugular bulb
Steeple’s sign Loss of normal shouldering of the air column due to
Stankiewicz’s sign Fat protrudes into nasal cavity on compression of
Tea pot sign Start of dribbling of CSF from nose when a patient
Tear drop sign Tear drop-shaped opacication seen hanging from
Uvula pointing sign When scleroma involves the nasopharynx, uvula
Aquino’s sign Blanching of tympanic mass when a gentle pressure
Barber chair sign/
Lhermitte’s sign
Bezold’s sign Inammatory oedema at the tip of mastoid process Descending mastoiditis
Bocca’s sign Absence of postcricoid crackle (Muir’s crackle) Ca postcricoid
Brudzinski sign Bending of patient’s neck usually produces exion
Bryce’s sign Manual compression may result in escape of uid
Griesinger’s sign Oedema in postmastoid area due to mastoid
Increased vascularity in submucous layer of
promontory
oedema of tracheal mucosa
eye from outside
comes to sitting position from supine
roof of maxillary sinus on X-ray PNS
points towards nasopharynx
is applied over carotid artery
It is electric shock-like sensation in the spine and
extremities
of knee and hip
and gas in airway—a gurgling sound
emissary vein
Glomus jugulare
Active stage of otosclerosis
Glomus tumour
Aberrant ICA
ALTB
Orbital injury during FESS
CSF rhinorrhoea
Orbital oor fracture
Rhinoscleroma involving
nasopharynx
Glomus jugulare
Post-RT of cervical spine
Meningitis
Laryngocoele
Lateral sinus thrombophlebitis
(continued)

2.8 Signs ofENT andHead andNeck Surgery Diseases
Table 2.8 (continued)
Sign Denition Diagnosis
Berry’s sign Absence of carotid pulse when it engulfed Thyroid carcinoma
Enroth’s sign Chemosis and oedema of conjunctiva and lids
Hitselberger’s sign Loss of sensation in posterosuperior part of EAC Acoustic neuroma
Holman-Miller sign
(antral sign)
Halo sign/
handkerchief sign
Hennebert’s sign Pressure-induced dizziness Meniere’s disease/congenital
Hondousa sign Widening of gap between ramus of mandible and
Irwin Moore’s sign Positive squeeze test Chr. tonsillitis
Laugier’s sign Blood behind TM Skull base fracture
Light house sign Small pin hole perforation with pulsatile ear
Lyre’s sign Bowing with displacement of carotid artery due to
Leudet’s sign Clicking sound tinnitus, caused by reex spasm of
Milian’s ear sign Erysipelas can spread to pinna but not cellulitis Erysipelas
Trotter’s sign/triad U/L COHL, trigeminal neuralgia, soft palate
Rising sun sign in
neck
Battle’s sign Bluish discoloration over mastoid Fracture of temporal bone
Chvostek’s sign Spasm of facial muscle when tapped It is sign of hypocalcaemia
Dodd’s sign/
Crescent’s sign
Furstenberg’s sign Pulsation and expansion of the mass with crying,
Trousseau’s sign Carpopedal spasm upon constriction of extremities Hypocalcaemia
Thumb sign Thumb-like impression on X-ray lateral view due to
Charcot’s triads Nystagmus, scanning speech, intention tremors Multiple sclerosis
Browne’s sign Blanching noted when pressure applied with
Anterior bowing of the posterior wall of maxillary
sinus on X-ray face lateral view
CFS separates from blood when the mixture is
placed on paper resulting in central blood with outer
ring of CSF
maxillary border
discharge
vascular mass on bifurcation of carotid artery
the tensor palati muscle
immobility and trismus
Lower border of lymph node is not palpable of
supraclavicular lymph node
Crescent of air seen between mass and posterior
pharyngeal wall
straining or compression of jugular vein
swollen epiglottis
Siegel’s speculum to tympanic membrane
JNA
CSF rhinorrhoea
syphilis
Infratemporal involvement of JNA
ASOM
Carotid body tumour
Inammation of ET
Nasopharyngeal carcinoma
Nodal metastasis in level Vb group
of LN due to carcinoma stomach
It is positive in AC polyp and absent
in JNA
Encephalocoele
Acute epiglottitis
Glomus tumour
73

74
2 Local Examination ofORL: Head andNeck Surgery
2.9 Syndrome inENT andHead
andNeck Surgery (Table2.9)
Table 2.9 Various syndrome of otolaryngology and head and neck surgery
Name of syndrome Denition
Arhinia choanal atresia
microphthalmia
Anterior ethmoidal nerve
syndrome (Sluder’s
neuralgia)
Ramsay Hunt syndrome,
type 2
Eagle’s syndrome It is syndrome characterized by elongation of styloid process and calcication of
Crouzon syndrome It is a genetic disorder, also known as branchial arch syndrome characterized by
Von Hippel-Lindau Retinal angiomas, cerebellar haemangioblastoma
Frey’s syndrome It is also known as gustatory sweating
Supermarket syndrome Dizziness+nausea+light headedness induced by light and shelves and crowd
Syndrome associated with cleft palate
Pierre Robin syndrome Micrognathia+glossoptosis+cleft palate
Treacher Collins
syndrome
Nagar’s acrofacial
dysostosis
Goldenhar syndrome It is a rare congenital disorder characterized by abnormal development of eye ear and
Mobius syndrome It is a rare congenital neurological disorder characterized by facial palsy and inability
Hallermann-Streiff
syndrome
Gordon’s syndrome Camptodactyly+club feet+cleft palate
Syndrome associated with hearing loss
Craniofacial deafness
hand syndrome
Mal de debarquement
syndrome
Susac’s syndrome Encephalopathy, retinal artery occlusion and SNHL
Cogan’s syndrome B/L SNHL, episodic dizziness and B/L interstitial keratitis
Syndrome autosomal
dominant
Waardenburg syndrome
(most common)
Branchiootorenal
syndrome
Stickler syndrome Hearing loss (SNHL, COHL or MHL) may be progressive
Aplasia/hypoplasia of nose+microphthalmia and midface retrusion
It is presented as ipsilateral foreheadache due to irritation of anterior ethmoidal nerve
ending in nose. This is caused by septal spur touching middle turbinate
It is also known as herpes zoster oticus caused by reactivation of herpes zoster in
geniculate ganglion. It is presented as LMN facial palsy, vesicle on face and ear,
deafness, vertigo and ear pain
stylohyoid ligament presented as throat pain, neck pain which radiates to ipsilateral ear
craniosynostosis (premature fusion of certain skull bones, exophthalmos, hypertelorism
and beak-like nose (psittacosis)); this syndrome is named after Octave Crouzon, a
French physician
It is a genetic disorder characterized by down slanting eye, notched lower eyelids,
small and slanting lower jaw, prominent ear and cleft palate
This disorder affects limb and face
spine. It is also known as oculoauriculovertebral syndrome. It is rst documented by
Maurice Goldenhar, an ophthalmologist
to move eye from side to side
It is a rare disorder characterized by distinctive malformation of the skull and facial
region, hypotrichosis, eye abnormality, dental defect, degenerative skin changes over
skull and nose
Aplasia/hypoplasia of nose+blepharophimosis+depressed nasal
bridge+downslanted palpebral ssure
A sensation of rocking or swaying back and forth without vertigo, difculty
concentration and fatigue, in idle age woman due to week long cruise
Clinical features
U/L or B/L SNHL, pigmentary changes—like greying hair, white forelock,
heterochromia iridis, partial albinism, facial features—fused eyebrows, high nasal
bridge, hypoplastic alae nasi
Hearing loss is COHL or MHL or SNHL
Others are preauricular sinus, branchial cyst or sinus, renal problem+Mondini
dysplasia
Micrognathia (small jaw) with cleft palate (Pierre Robin sequence)
(continued)

2.9 Syndrome inENT andHead andNeck Surgery
Table 2.9 (continued)
Name of syndrome Denition
CHARGE syndrome Coloboma, choanal atresia, cranial nerve problems and unusually shaped ears. Hearing
loss may be conductive, sensorineural or mixed (mild to profound)
Treacher Collins
syndrome
Neurobromatosis type
II (NFII)
Autosomal recessive syndrome
Usher syndrome type 1 SN hearing loss (profound and congenital), vestibular dysfunction (vertigo), no benet
Usher’s syndrome type 2 Moderate to severe, downward sloping, congenital SNHL No vestibular dysfunction
Usher’s syndrome type 3 Progressive, sensorineural hearing loss, later onset
Pendred syndrome Hearing loss is sensorineural and may be progressive
Jervell and LangeNielsen syndrome
X-linked syndrome
Alport syndrome Hearing loss is progressive and sensorineural
X-linked congenital
stapes xation with
perilymph gusher
Mitochondrial
Maternally Inherited
Diabetes and Deafness
(MIDD)
Kearns-Sayre syndrome
(KSS)
Biotinidase deciency Hearing loss in >75% of cases, skin rashes, alopecia, seizure, ataxia
Albinism deafness
syndrome
Alport’s syndrome It is characterized by kidney disease, hearing loss and eye problem (anterior lenticonus
Albinism deafness
syndrome (ALDS)
Abruzzo-Erickson’s
syndrome
Art’s syndrome SNHL+hypotonia+ataxia
Stickler syndrome It is a group of vary rare genetic disorder (progressive arthro-ophthalmo-dystrophy)
Syndrome of head and neck
MEN IIA (Sipple
syndrome)
MEN IIB RET mutation+mucosal neuroma
Hearing loss (conductive), malar hypoplasia, microtia/anotia, stenosis/atresia of EAC,
ear tag, etc.
Progressive hearing loss (SNHL), B/L, acoustic neuroma by 30years of age
with hearing aid
Inner ear malformations (Mondini malformation) may be present
Balance dysfunction is present, enlarged thyroid gland (goitre)
Bilateral, profound sensorineural hearing loss is present at birth
Abnormal heart rhythm (long Q-T)
Syncopal episode and possible sudden death
Kidney problems (nephritis), near-sightedness (myopia)
Hearing loss in males is mixed and may be progressive
Hearing loss is sensorineural and often found in the high frequencies and diabetes
Hearing loss is bilateral and sensorineural, unsteady gait (ataxia), short stature, delayed
puberty, progressive paralysis of the eye, muscles (ophthalmoplegia) and progressive
blindness (retinopathy)
A rare disorder characterized by congenital nerve deafness (SNHL) and pie baldness
with no ocular albinism
or maculopathy)
Hypopigmented skin patches, neurological speech impairment and SNHL and partial
albinism
Cleft palate+ocular coloboma+hypospadias+SNHL
affecting connective tissue, especially collagen. It is characterized by distinct facial
abnormality, ocular problem, hearing loss, joint and skeletal problem
RET proto-oncogene chromosome 10 mutation+medullary
carcinoma+pheochromocytoma+parathyroid hyperplasia
75

History andExamination ofEar
3
3.1 Symptoms/History/Chief
Complaints ofEar Diseases
1. Symptoms/chief complaints—There are var-
ious common symptoms with which patients
can present to ENT surgeon. These common
symptoms are ear discharge, hearing loss,
pain, tinnitus, vertigo, injury/trauma, facial
palsy, deformity, foreign body, swelling,
bleeding and vesicle. Patients can present
with single symptoms or combination of
symptoms.
(a) Ear discharge—This is one of the com-
monest symptoms of infective ear
diseases.
• Duration of discharge
– Acute discharge (if duration is less
than 12 weeks)—ASOM, trauma,
CSF otorrhoea or furunculosis.
– Chronic discharge (if duration is
more than 12 weeks)—CSOM,
allergic, cholesteatoma.
• Onset of discharge
– Sudden onset (discharge develops
abruptly)—CSF otorrhoea, bleeding, ASOM.
– Gradual/insidious onset (discharge
develops slowly)—CSOM,
otomycosis.
• Colour of discharge—The discharge
has been classied into various types
depending on colour of discharge
(Table3.1).
• Consistency of discharge
– Thin discharge (it is watery so that it
can ow easily) caused by ASOM,
CSF otorrhoea, eczematoid dermatitis, acute infection in CSOM.
– Thick discharge (thick, stick to
wall) caused by CSOM, cholesteatoma, wax, otomycosis, tubercular
otitis media (OM), furunculosis,
allergic otitis media.
• Type of discharge—The various
types of ear discharge have been
reported (Table3.2).
Table 3.1 Different colours of ear discharge with differential diagnosis
Colour of discharge D/D
Colourless CSF otorrhoea, acute otitis
media
Yellow CSOM with bacterial infection
Reddish (discharge
mixed with blood)
White Otomycosis (candida), CSOM,
Brown Wax
Black Otomycosis (Aspergillus niger)
Red/bleeding Granulation, haemangioma,
Greenish Aspergillus fumigatus
CSOM with granulation,
ASOM, CSOM with
cholesteatoma
ASOM
trauma, glomus tympanicum
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2025
S. K. Kashyap, S. Sagar, Clinical Methods of Otorhinolaryngology, Skull Base & Head Neck
Surgery, https://doi.org/10.1007/978-981-96-1765-4_3
77
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