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Examination of Jaw
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Investigations for Jaw Disease
1. Orthopantomogram (OPG): It is a plain X-ray
of the jaw and mandible which shows the entire mandible and partly maxilla in a single plane. It is better than X-ray mandible lateral view as it highlights proper dentition, inner and outer plates of mandible (Figs 11.12A and B). It is a rotational tomogram. Indications: Jaw tumours—adamantinoma, dental cyst, dentigerous cyst, osteoclastoma; osteomye­litis of the mandible; fracture mandible; to see infiltration in carcinoma of oral cavity.
2. CT scan of jaw including neck and base of skull
in maxillary diseases, tumours, trauma to assess extent. Sinus endoscopy.
3. Biopsy, discharge study, culture of discharge,
FNAC of lymph node.
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sphenoids are next in order. It is common in people working in furniture industries, mustard gas industries, and leather industries. It is common in Bantus in South Africa where snuff with nickel and chromium is commonly used. Squamous cell carcinoma is the commonest type – 80%. Adenocarcinoma, transitional cell carcinoma, salivary tumours, sarcomas, melanoma and Burkitt’s lymphoma also can occur (Fig. 11.13).
Maxillary Tumours
They are rare. Maxillary sinus is the commonest site of malignancy in paranasal sinuses. Ethmoids, and
A
B
Figs 11.12A and B: Orthopantomogram being taken
and X-ray OPG look.
Fig. 11.13: Extensions of tumour from maxillary
antrum.
Behaviour and Presentation
Initially may be asymptomatic or may present with epistaxis or features of chronic sinusitis. When it spreads to the floor, loosening of the teeth, necrosis, antro-oral fistula can occur. Extension medially causes nasal block, fungation, nasal discharge, blockage of nasolacrimal duct (epiphora). Extension anteriorly causes pain, anaesthesia and swelling in the cheek, ulceration and fungation in the skin of cheek. Spread above into the orbit causes epiphora, diplopia, proptosis. Posterior spread is most dangerous as it is not revealed easily. It causes postnasal discharge, pain, trismus, limitation of movement of temporo­mandibular joint. Involvement of upper deep cervical lymph nodes in later stage is common.
Differential diagnosis: Chronic sinusitis.
Classification
Ohngren’ s classification: An imaginary plane is drawn extending between medial canthus of eye and the angle of mandible. Growth situated above this plane is called as suprastructural which has got poor prognosis. Growth below this plane is called as infrastructural and has got better prognosis (Fig. 11.14).
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Fig. 11.14: An imaginary plane is drawn extending between medial canthus of eye and the angle of mandible and line in this plane is called as Ohngren’s line.
SRB’s Clinical Surgery
Lederman’s classification: Two horizontal lines are
used, one passes through the floor of the orbit, another passes through the floor of the antra. These lines are called as line of Sebileau. (1) Suprastructure type: In this type olfactory area of nose, ethmoidal, sphenoid, and frontal sinuses are involved. (2) Mesostructural type: This involves maxillary sinus and nasal respiratory part. (3) Infrastructural type: This type involves alveolar process. Lederman’s classification is further divided by two vertical lines over medial walls of the orbit to separate ethmoid sinuses and nasal fossa from maxillary sinuses (Fig. 11.15).
Diagnosis: X-ray of the part-opacity of the involved sinus with destruction of bony walls is seen. CT scan is ideal method (Figs 11.16A and B). Biopsy is done through nasal/oral route or on early stage through
TNM staging Staging
T1 Tumour limited to antral mucosa Stage I T1 N0 M T2 Tumour causing bone erosion/destruction including extension into Stage II T2 N0 M
hard palate or middle meatus of nose. Stage III T3 N0 M0,
T
Tumour invading bone of posterior wall of maxillary sinus/skin of T1/T2/T3 N1 M
3
cheek/medial wall of orbit/infratemporal fossa/pterygoid plates/ Stage IVA T4 N0 M0, T4 N1 M ethmoid sinuses. Stage IVB Any T N2 M0,
Tumour invading orbital contents beyond the floor or medial wall Any T N3 M
T
4
including orbital apex/cribriform plate/base of skull/nasopharynx/ Stage IVC Any T Any N M sphenoid or ethmoidal sinuses.
Fig. 11.15: Diagrammatic representation of Lederman classification.
0 0
0
0
0
1
A
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B
Figs 11.16A and B: Carcinoma maxillary antrum
and CT picture.
Examination of Jaw
swelling from the gum which is firm and bleeds on touch.
Fibrous epulis: It is a benign condition, can occur in any individual. It is the commonest type of epulis; it is firm or hard, commonly sessile rarely pedunculated slow growing benign fibroma arising from periodontal membrane. It is painless, well localised, hard/elastic, non-tender gray-pink swelling in the gum which bleeds on touch. It mimics squamous cell carcinoma. OPG; biopsy from the lesion is essential. Recurrence can occur if root is not removed properly.
Pregnancy epulis: It occurs in pregnant women due to inflammatory gingivitis usually during 3rd month of pregnancy. Clinically it resembles fibrous epulis or pyogenic granuloma. It usually resolves after delivery; otherwise it should be excised.
Granulomatous epulis: It is a mass of granulation tissue in the gum around a carious tooth. It is soft, bright red swelling which bleeds while brushing.
Myelomatous epulis: It is seen in leukaemic patients. Investigated for leukaemia by peripheral smear, bone
marrow aspiration and biopsy. Giant cell epulis: It is osteoclastoma causing ulceration
and haemorrhage of gum. It is painless expanding swelling in mandibular part.
Carcinomatous epulis: It is squamous cell carcinoma of the alveolus and gum presenting as localised, hard, indurated swelling with ulceration.
Fibrosarcomatous epulis : It is fibrosarcoma arising from fibrous tissue of the gum. It is with variable consistency often softer, bluish red, progressive swelling which bleeds on touch.
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Caldwell-Luc operation. Sinus endoscopy is done for detailed examination of sinus and for biopsy.
Epulis
Swelling arising from the gums is called as Epulis (gumboil, upon gum—Greek).
Congenital epulis: It is a benign condition seen in a newborn arising from gum pads. It is a variant of granular cell myoblastoma originating from gums. It is more common in girls. It is more common in upper jaw. It is not a malignant condition. It is well localised
Jaw Tumours
Classification
Swelling arising from the gums (Epulis): Congenital epulis; Fibrous epulis; Pregnancy epulis; Giant cell epulis; Myelomatous epulis; Sarcomatous epulis.
Swelling arising from the dental epithelium (Odon- tomes): Benign odontogenic tumours: Epithelial
Ameloblastoma; Calcifying odontogenic tumour; Odontogenic adenomatoid tumour; Enameloma; Composite odontoma, which may be either complex or
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SRB’s Clinical Surgery
compound. It is odontogenic hamartoma containing all 4 layers—dentin, enamel, cementum and pulp. Mesodermal tumour: Odontogenic fibroma, myxoma; Cementoma, dentinoma. Malignant odontogenic tumours: Malignant ameloblastoma; Fibrosarcoma.
Cysts arising in relation to dental epithelium: Dental cyst; Dentigerous cyst.
Swelling arising from the mandible or maxilla:
Osteoma and osteoblastoma; Torus palatinus and mandibularis; Fibrous dysplasia; Osteoclastoma; Osteosarcoma; Secondaries.
Surface tumours: Tumours from the surface which extend into the jaw (Fig. 11.17) .
Clinical features: Swelling in the jaw usually in the mandible near the angle extending to vertical ramus
which attains a large size. It is gradually progressive, painless, smooth and hard with intact inner table. Outer table expansion is typical. Lymph nodes are not enlarged. It is common in males; common in 5th decade. It should be differentiated from osteoclastoma of mandible (here inner table is not intact); dentigerous cyst; dental abscess. Condition is curable by proper surgery . Recurrent adamantinoma can spread through blood. OPG shows eccentric expansion of the angle and vertical ramus of the mandible with trabeculations – honeycomb look (Fig. 11.18).
Fig. 11.17: Large jaw tumour – could be
adamantinoma or osteoclastoma.
Ameloblastoma (Adamantinoma [Greek Adamas – strong/unconquerable], Eve’s disease, Multilocular cystic disease of the jaw)
It arises from the dental epithelium probably from the enamel/dental lamina. It occurs commonly in mandible
or maxilla. Occasionally it is seen in the base of the skull in relation to Rathke’s pouch or in tibia. Histologically it is a variant of basal cell carcinoma. It is a locally malignant tumour. It neither spreads through lymph node nor through blood. Hence it is curable. It is usually unilateral. It can occur in a pre­existing dentigerous cyst. It is multilocular but can be unilocular.
Fig. 11.18: X-ray showing adamantinoma
with honeycomb look.
Curable malignancies
Adamantinoma Basal cell carcinoma Verrucous carcinoma Papillary carcinoma thyroid Marjolin’s ulcer Carcinoma colon
Dentigerous Cyst (Follicular Odontome)
It is a unilocular cystic swelling arising in relation to the dental epithelium from an unerupted tooth. It is common in lower jaw (in relation to premolar or canine), but can also occur in upper jaw; It occurs over the crown of unerupted tooth; commonly seen in relation to premolars or molars (Fig. 11.19). It causes expansion of outer table of the mandible; it is solitary and unilocular containing glairy fluid; histologically contains enamel derived squamous cells; common in younger age group; presents as painless swelling in the jaw which is smooth and hard; egg shell crackling
Examination of Jaw
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Fig. 11.19: Dentigerous cyst.
often may be present. It mimics dental cyst, adaman­tinoma, osteoclastoma. It can turn into adamantinoma. OPG shows well circumscribed translucent area in the jaw with permanent unerupted tooth within it (Fig.
11.20).
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derived by epithelial debris of Mallassez. It is an infective granuloma with epithelial proliferation which later gets degenerated to cause cystic fluid in the cavity. It is unilocular; contains mucoid material and cholesterol crystals; presets as a smooth, tender localized swelling in the jaw with exapansion in relation to caries tooth; common in adult; common in maxilla adjacent to upper incisor or canine. OPG shows circular radiolucent area with clear often sclerosed margin in relation to the tooth of the maxilla. It can cause osteomyelitis of the mandible (Fig. 11.21).
Dental Cyst (Radicular Cyst, Periapical Cyst)
It occurs under the root of a chronically infected dead erupted tooth. It is lined by squamous epithelium
Fig. 11.20: Orthopantomogram showing dentigerous cyst.
Differences between Dental cyst and Dentigerous cyst:
Dental cyst Dentigerous cyst
Site Maxilla – incisor / canine Mandible – premolar / molar Type of tooth Erupted infected tooth often dead tooth Unerupted permanent tooth Location Under the root of tooth Over the crown of the tooth Age Adult Younger age group Complication Osteomyelitis Adamantinoma
Fig. 11.21: Dental cyst.
Solitary Bone Cyst
It occurs in premolar or molar region of the mandible. Rounded cyst bulges outwards. Bone resorption with bone deposition in the margin is common. Fluid is yellowish with high bilirubin content. Haemorrhage with clot formation is known to occur.
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Ossifying Fibroma
SRB’s Clinical Surgery
It occurs exclusively in jaw bones. It is common in young girls. In upper jaw it fills the maxillary antrum and later presents as well localised external swelling. Initial rapid growth ceases eventually and becomes stationary. Alignment of teeth is known to occur. X-ray shows soft tissue shadow with scattered bone deposition.
Fibrous Dysplasia
It is a self limiting disease where the medullary/spongy bone is replaced with fibroosseous tissue. It can be monoostotic or polyostotic. Monoostotic is common in long bones. In polyostotic type mandible also is commonly involved. Maxilla can be involved occa­sionally. It is crab flesh white in colour; containing islands of cartilages and cystic spaces. It can be bilateral in mandible (Fig. 11.22A). It presents as painless
swelling in the mandible of growing children; common in females; showing expansion of outer cortex but teeth are normal. Treatment is done only after cessation of skeletal growth. X-ray shows typical area of ‘smoke screen translucency’ (Fig. 11.22B). Polyostotic fibrous dysplasia; pigmentation of the skin; precocious puberty in females is – Albright’s syndrome.
Osteoclastoma (Giant Cell Tumour) of Mandible
It is giant cell tumour arising from epiphysis in young adults; common in long bones; can occur in mandible. It can be benign/intermediate or malignant (10%). Expanding swelling towards inner table of the mandible with cystic spaces; egg shell crackling; discontinuity in inner table are typical. Central part of the jaw either mandible (common) or maxilla is involved (in mandible body is commonly involved). When it is malignant spread can occur to lungs. Pathological fracture is known to occur. Displaced roots of adjacent teeth, loose teeth are common. Giant cells are due to fused spindle cells (not due to osteoclasts-misnomer). Giant cell epulis, brown tumour of hyperparathyroidism, dentigerous cyst and adamantinoma are differential diagnosis. X-ray and biopsy confirms the diagnosis.
A
B
Figs 11.22A and B: Fibrous dysplasia of mandible (A)
and X-ray picture (B).
Giant Cell Reparative Granuloma (Jaffe Tumour)
It is a swelling which occurs due to haemorrhage within the bone marrow . It contains vascular stroma, collagen and connective tissue cells. It is common in women. It causes painless enlargement of jaw . It can be treated by calcitonin (100 units/0.5 mg subcutaneously daily for 12 months) or surgical curettage.
Upper Jaw Tumours
Ivory osteoma, osteoclastoma, osteosarcoma, squa­mous cell carcinoma of maxillary antrum, carcinoma of hard palate are the examples (Fig. 11.23).
Lower Jaw Tumours
Fibrous dysplasia is common in mandible as it develops partly from membrane. Paget’s disease of jaw, osteoclastoma, oral malignancy infiltrating the mandi­ble are common types (Fig. 11.24).
Fig. 11.23: Upper jaw tumour—from maxilla causing proptosis.
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Fig. 11.24: Lower jaw tumour—could be
adamantinoma mandible.
Examination of Jaw
Alveolar Abscess (Dental Abscess)
It is due to spread of infection from root of the tooth into the periapical tissue. Initially it forms periapical abscess which later spreads through the cortical part of the bone into the soft tissues around forming an alveolar abscess. Disease begins in the pulp of tooth pulpitis spread to root localised osteitis abscess formation spread into soft tissues outside in cheek initially diffused later localised swelling in the jaw with redness and oedema of gum. Initial dull continuous pain later becomes severe excruciating pain. Fever, trismus, often dysphagia, palpable tender neck lymph nodes occur eventually . Oedema, pain in the floor of the mouth may occur (Fig. 11.25). Swelling may burst spontaneously to form a sinus outside.
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Burkitt’s Lymphoma
It is multifocal childhood lymphoma common in Africa probably due to Epstein-Barr virus. It can occur in upper or lower jaw . It is common in premolar or molar area. When many areas are involved it occurs on same side of both maxilla and mandible. Disease expands outwards involving cheek and soft tissues outside. Lamina dura of teeth disappears. Neck nodes may get enlarged; retroperitoneal mass; hepatomegaly; ovarian tumour; renal, adrenal, pancreatic and mesenteric nodal involvement are common. Involvement of spinal nerves, salivary gland, breast, thyroid, bones, intracranial spread, and cranial nerve palsies are known to occur. Typical starry sky pattern in histology is obvious.
Fig. 11.25: Typical dental abscess.
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SRB’s Clinical Surgery
Bacteria: Staphylococci, streptococci, anaerobic bacteria and gram-negative organisms. Alveolar abscess occurring in relation to upper lateral incisor will not present outside but produces swelling on the palate medially. Abscess in relation to wisdom tooth also opens medially (not outside) and may cause Ludwig’s angina. X-ray will reveal rarefaction of the root of the tooth only after 10 days.
Complications: Septicaemia; spread of infection into other spaces like parapharyngeal spaces; sublingual and submandibular spaces causing Ludwig’s angina; oedema of epiglottis and respiratory distress; spread to pterygoid space and along pterygoid muscles through emissary vein cavernous sinus thrombosis; upper canine tooth abscess medial corner of eye angular vein thrombophlebitis cavernous sinus thrombosis; submasseteric abscess; lower incisor abscess can cause abscess in the chin and later median mental sinus; chronic osteomyelitis of the jaw with discharging sinuses.
Osteomyelitis of Jaw
It can be in the maxilla or mandible. Causes: Alveolar abscess leading into osteomyelitis;
recurrent dental infection; trauma; after dental extraction; surgeries of the jaw; postradiotherapy osteomyelitis (osteoradionecrosis).
Types: Acute: Common in children; maxilla or mandible may get involved (Fig. 11.26); swelling, redness, fullness is the features; pus may trickle through nostril if it is in maxilla. Subacute: It is the commonest type; common in adult; apical sepsis, endarteritis, bone necrosis is the pathology; common in mandible; rare in maxilla due to existing network vasculature which prevents endarteritis. Compression over inferior dental nerve causes numbness in chin in distribution area of mental nerve. Pain, swelling, tenderness, irregularity, thickening are typical. Chronic: It is also common in mandible; apical abscess, alveolar abscess, trauma, radiation, chemical like phosphorus, tuberculosis, syphilis, actinomycosis are the causes. Pain, thickening, irregularity, discharging sinus, sequestrum in the discharge, discomfort are the features. Infection from lower incisor causes median mental sinus. X-ray shows features of osteomyelitis with new bone formation and sequestrum.
Fig. 11.26: Osteomyelitis of mandible.
Actinomycosis: Faciocervical is the commonest type; lower jaw is commonly involved; infection begins at carious tooth; indurated gums nodules abscess multiple sinuses discharging sulphur granules with normal X-ray (Ray fungus) Actinomycosis israelii is the causative agent.
Cherubism (Cherub–Angelic Being)
It is an autosomal dominant familial condition occur­ring in first year of life. It shows giant cell granuloma with fibrous tissues in the jaw. It is commonly bilateral; commonly seen in angles of the mandible and also in maxilla. It presents as diffuse enlargement of maxilla and both sides of the mandible; bulging of the cheek causes pull of the lower eyelid. Hence child appears like, as if looking upwards (winged face of angelic babies); interference of the development and eruption of the teeth. It is a self limiting disease. Often requires dental care and treatment for proper dentition.
Treacher-Collins Syndrome
It consists of mandibulofacial dystosis; hypoplasia of the zygomatic bone and mandible; antimongoloid slant to the palpebral fissure; coloboma of lower eyelid; Low ear lobule with deficient middle ears. It is familial.
Pierre-Robin Syndrome
It is a congenital entity consisting of – cleft palate alone; mandibular hypoplasia; cyanotic episodes, deficiency in transforming growth factor; defective
Examination of Jaw
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sucking and tongue falling backwards in infants, cryptorchidism.
Micrognathism and Prognathism
Excessively small mandible is called as micrognathism. Backward displacement of tongue in neonates with micrognathism can cause respiratory distress. Here oral cavity is small. Prognathism is where mandible is larger than average with protrusion. Occasionally maxilla is hypoplastic.
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Soft-tissue injuries: Lacerations, contusions, cut wounds, etc; Eyelid injuries with black eyes; Facial nerve injury; parotid duct injury; lacrimal apparatus injury.
Injuries to the facial bones: Fracture nose—Patient presents with pain and swelling in the nose with deviation and displacement. Injuries to the maxilla; zygomatic bone injuries; mandibular bone fracture and mandibular dislocation; orbital bone fracture: presents with diplopia, enophthalmos, infraorbital nerve sensory loss.
Diseases of the Palate
Cleft palate; Torus palatinus—a bony hard swelling in the centre of the hard palate; nasopalatine cysts; Epstein’ s pearls at the junction of soft and hard palates in the midline in infants due to retained developmental cell rests; apical cyst or abscess; minor salivary gland tumour—commonest site is palate; Maxillary tumour extending into the palate; Squamous cell carcinoma of the palate; gummatous perforation in the middle of the palate seen in congenital syphilis; perforation of the palate anywhere in carcinoma palate.
Nasopalatine Cyst
It develops in incisive canal; causes spherical bone cavity behind upper incisors; composed of epithelial lining with fibrous capsule with mucous secreting cells. It occurs in the midline of palate.
Maxillofacial Injuries
It may be due to road traffic accidents, assaults, bullet injuries or sport injuries.
Classification
Fracture in maxillofacial region can be grouped as:
Fracture lower third that comprises mandible; Fracture middle third that comprises maxilla, zygoma and nose; Fracture upper third of the face involving part of the orbit, frontal bones.
Maxillofacial fracture also can be grouped as:
Fracture of the face which do not involve the dental occlusion; fractures of zygoma and nose; fracture which involves the dental occlusion; fracture mandible and maxilla.
Respiratory Obstruction
Causes: Oronasal airway block can occur by blood, clot, vomitus, foreign body, dentures, teeth, saliva, bone pieces, etc; Backward falling of tongue can cause obstruction of the nasopharynx and oropharynx. It is common in bilateral mandibular fracture; occlusion of the nasopharynx and oropharynx can occur in fracture maxilla with posterior and inferior displace­ment; haematoma in floor of the mouth or posterior oral cavity can cause airway block; other features include oedema of larynx/tongue/posterior third of oral cavity/pharynx; surgical emphysema.
Haemorrhage in Maxillofacial Injuries
Haemorrhage in maxillofacial injuries is usually not life threatening. But it should be identified and controlled properly . In association with other internal injury , such haemorrhage may be important to cause the circulatory failure. Haemorrhage may be due to— Soft tissue bleeding; bleeding from inferior alveolar artery, palatine vessels; nasal bleeding.
Clinical Features
Localised swelling due to haematoma; facial oedema; bleeding with open wounds; asymmetry which is clinically confirmed by observing supraorbital ridges, nasal bridge; localised tenderness; step deformity; trismus; diplopia; features of associated injuries like intracranial, abdominal or thoracic injuries.
Investigations: X-ray face; CT scan of head/jaw. General treatment for faciomaxillary injuries:
Suturing of soft tissues; Airway maintenance; Control
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of bleeding; Pain relief; Control of infection; Treating the individual fractures (Fig. 11.27).
Fracture Middle Third Area
It includes—maxillae, zygomatic bones, palatine bones, nasal bones, lacrimal bones, inferior conchae (one on each side), the vomer, ethmoid and its attached conchae, pterygoid plates of sphenoid.
Fracture middle third includes fracture maxilla, zygoma and nasal bones.
Fractures not involving occlusion Fractures involving occlusion
Central Dentoalveolar
• Fracture nasal bones and or nasal septum
• Fracture of frontal process of maxilla Subzygomatic
• Fractures of above two extending into • Le Fort I-low level either unilateral or bilateral ethmoid- nasoethmoid • Le Fort II-pyramidal either unilateral or bilateral
• Fractures above three which extends into frontal bone – fronto-orbito-nasal dislocation Suprazygomatic Le Fort III –high level
Lateral
• Fractures involving zygomatic bone, arch and maxilla excluding the dentoalveolar component
SRB’s Clinical Surgery
Zygomatic Complex Fracture
Classification
Simple fracture which is stable and undisplaced— Here fracture line passes across the infraorbital foramen downwards over anterior wall of the antrum.
Simple fracture which is displaced medially. It may be associated with rotation/tilt in vertical axis, either
• Craniofacial disjunction—unilateral or bilateral
Le Fort classification (Fig. 11.28)
(Rene Le Fort – French surgeon classified these fractures by dropping rocks on the face of the cadavers and later dissecting the area for study and research and published paper in 1911)
Types Features
Le Fort I (Guerin’s fracture-low level) • Bleeding from nose (floating fracture, horizontal fracture of maxilla) • Posterior gagging of occlusion
• It runs horizontally above the floor of the nasal • Upper lip swelling cavity involving lower third septum, palate, alveolar • Palatal echymosis process of maxilla and lower third of pterygoid • Occlusion derangement plates of maxilla • Floating maxilla
Le Fort II (pyramidal fracture) • Oedema of middle third face
• From the nasal bones at topmost, fracture runs • Both sides circumorbital and subconjunctival laterally towards lacrimal bones, medial wall of orbit, ecchymoses infraorbital margin, through or medial to infraorbital • Nasal bleeding/obstruction/deformity foramen and backwards below the zygomaticomaxillary • Deformity of face (dish face), diplopia area through lateral wall of maxillary sinus and pterygoid • Retroposition of maxilla with posterior gagging plates. Zygoma is intact with skull base • Limitation of ocular movements, CSF rhinorrhoea
Le Fort III (craniofacial disjunction, high level) • Lengthening of face
• Here fracture runs parallel to skull base. It passes • Enophthalmos, ocular level depression through the nasal bone, lacrimal bone, ethmoid bone, • Hooding of eyes, occlusal plane tilting optic foramen, inferior orbital fissure, pterygomaxillary • Entire facial skeleton moves as a single block fissure and lateral orbital wall with frontozygomatic • Tenderness and separation of suture line suture with zygomatic arch • Diplopia
• Tenderness and separation of infraorbital margin
• Trismus, teeth mal-alignment Guerin sign: Haematoma at greater palatine foramen