This document discusses sinonasal tumours, including:
1. It classifies sinonasal tumours by tissue of origin such as epithelial, neuroendocrine, soft tissue, bone, etc. and lists examples of benign and malignant lesions within each tissue.
2. It provides details on specific benign tumours such as inverted papilloma, haemangioma, and juvenile angiofibroma.
3. It also discusses malignant tumours of the sinonasal region like squamous cell carcinoma, adenocarcinoma, olfactory neuroblastoma and haemangiopericytoma.
Maxillectomy and craniofacial resection Mamoon Ameen
all maxillectomy types in detail and maxillofacial resection ,indications ,contraindications ,preoperative asssessment and detail techniques and rehabilitations
Maxillectomy and craniofacial resection Mamoon Ameen
all maxillectomy types in detail and maxillofacial resection ,indications ,contraindications ,preoperative asssessment and detail techniques and rehabilitations
Cavity obliteration is a procedure done at the end of Mastoidectomy to get a cavity-less mastoid cavity thus solving the problem of discharging post-operative cavity.
Spaces of middle ear and their surgical importanceDr Soumya Singh
one of the imp topics in ENT that should be understood very thoroughly if u want to pursue as an otologist.I tried to simplify the topic with simple diagrams and models for better understanding .
Cavity obliteration is a procedure done at the end of Mastoidectomy to get a cavity-less mastoid cavity thus solving the problem of discharging post-operative cavity.
Spaces of middle ear and their surgical importanceDr Soumya Singh
one of the imp topics in ENT that should be understood very thoroughly if u want to pursue as an otologist.I tried to simplify the topic with simple diagrams and models for better understanding .
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- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
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Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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3. Epidemiology:
1. 0.5% of all body cancers
2. 15% of all upper respiratory neoplasm
3. Maxillary Sinus is most common
4. 80-85% are Squamous Cell Carcinoma
5. Male : Female = 2:1
6. Age group: 45-65 years
7. Most common adult sinonasal malignancy: SCC
8. Most common paediatric : Rhabdomyosarcoma
9. Maxillary sinus > Nasal cavity > Ethmoid sinus
4. Risk Factors:
a. Hardwood dust ( Adenocarcinoma)
b. Softwood dust ( Squamous Carcinoma)
c. Nickel Refining, Chromium workers
d. Boot , shoe and textile workers
e. Mustard gas exposure
f. Human Papilloma Virus
g. Long standing Dentigerous Cyst
h. Exposure to radiation
5. Benign Neoplasm of Nasal Cavity
A. Squamous Papilloma :
Verrucous lesions similar to skin wart.
Involves nasal vestibule / lower nasal septum
Single/ Multiple; Sesile / Pedunculated
Tt: Cauterisation /Cryosurgery/ Laser
B. Papilloma of the Nose
Male: Female = 3:1
Age 30-50 year
3 types: 1. Fungiform : 50% , nasal septum, HPV +ve
2. Cylindrical: 3% , lateral wall/sinuses
3. Inverted Papilloma:47%, lateral wall
6. Inverted Papilloma:( Schneiderian papilloma)
4% of sinonasal tumours
Unilateral, local invasion, M>F, 50-70yr
Malignant potential 10 %( TCC, SCC)
Recurrence rate: 70 %
Microscopically proliferation of the covering epithelium and extensive
finger-like inversions into the underlying stroma of the epithelium.
U/L Nasal obstruction with Rhinorrhoea, epistaxis
D/D: AC polyp, AFRS, malignancy
7. Investigation
Biopsy: definite diagnosis
CT Scan: Hyper dense areas & calcification
coronal section – Cribriform Palm Tree Pattern
MRI: Enhancing mass in middle meatus with extension into maxillary
and ethmoid sinus. Heterogeneous Convoluted Cerebriform
appearance
Krouse’s Staging
Stage 1: Tumour limited to nasal cavity
Stage 2: Tumour limited to ethmoidal sinuses & medial & superior
portion of maxillary sinus
Stage 3: Tumours involves lateral & inferior aspects of maxillary
sinus or extension into frontal or sphenoid sinuses
Stage 4: Tumour spreads outside the confine of the nose and
sinuses
8. Resection :
• Initially via Trans-nasal resection: 50-80% recurrence
Via endoscopic surgery:
Type I- IP involving MM, E, SM, SS or combination
Type-II – Endoscopic medial maxillectomy- Nasoethmoidal complex not involving
anterior or lateral wall of the maxillary sinus
Type –III – Endonasal Denker / Sturman-Canfield – Anterior compartment of
Maxillary sinus
• Medial Maxillectomy via Lateral Rhinotomy
Gold Standard (only 10-20% recurrence)
indication: Benign & Malignant neoplasm limited to nasal walls & medial
wall of maxilla
• Inferior Medial Maxillectomy
• Endoscopic Medial Maxillectomy
Identify the origin of the papilloma
Bony removal of this region
9. Haemangioma
A: Capillary Haemangioma:
Bleeding polypus of the nasal septum
Soft , dark red, pedunculated / sesile
Epistaxis , Nasal obstruction
Local excision
B. Cavernous Haemangioma
Arises from the turbinate
Epistaxis , Nasal obstruction
Excision
10. Juvenile Angiofibroma:
• Highly vascular , benign but biologically aggressive tumour
with high incidence of persistence, recurrence.
• 0.5% of all head and neck tumour
• Exclusive to adolescent male ( 8-20 y)
• Most accepted theory ( Mild and Mauris hypothesis): JA
originates from sex steroid stimulated hammartomatous
tissue located in the turbinate cartilage
Histopathology:
Firm , slightly spongy lobulated swelling
Nodularity increases with age
Lack true capsule
Immature fibroblast in connective tissue stroma
Vascularization most often in periphery
11. Originates from the upper margin of Sphenopalatine
Foramen
Large tumour present as bilobed dumb bell swelling- one
component filling nasopharynx; other extending into
pterygopalatine and infratemporal fossa
Blood Supply:
Internal maxillary artery
Ascending pharyngeal artery
Vidian artery
Vertebral artery
• Spread : Medial: nasopharynx & nasal cavity
Lateral: pterygopalatine>infratemporal fossa>cheek
Posterior: medial pterygoid>lateral pterygoid
Anterior : Orbit through infra-orbit fissure
Superior : nasal cavity> sphenoid sinus
17. Chordoma:
Ethmoid , nasal cavity, nasal septum
Smooth , lobulated, firm
Surgical excision
Intranasal Meningoencephalocole
Herniation of brain tissues & meninges : Foramen caecum or Cribiform
plate
Smooth polyp in upper part of nose between the septum and middle
turbinate
Infants & young children
Increases size on crying or straining
Tt; Frontal Craniotomy, severing the stalk
from brain & repair dural & bony defect
18. Glioma;
o 30% are intranasal , 10% are both intra & extranasal
o Intranasal glioma presents as Firm Polyp
o Mostly infant & children
Nasal Dermoid:
o Widening of upper part of nasal septum with splaying
nasal bone & hypertelorism
o A pit or sinus in the midline of nasal
dorsum with hair protruding from
the opening
19. Malignant neoplasm- Nasal Cavity
Primary carcinoma per se rare- may be extension of maxillary or
ethmoid carcinoma
A. Squamous Cell Carcinoma:
Vestibular : arises from lateral wall of nasal vestibule extend to
columella, nasal floor, lip. Metastasis to Parotid
Septal : arises from mucocutaneous junction & causes burning &
soreness in nose. “ nose-picker’s cancer”
Lateral wall: extend into ethmoid or maxillary sinus. Presents as
polypoid mass.
Nasal obstruction, epistaxis, pain , cervical lymphadenopathy
Tt : Wide excision with 1 cm healthy margin
Radiotherapy
20. B. Adenocarcinoma & Adenoid cystic carcinoma
Arises from glands of mucous membrane or minor salivary glands.
Histologically: Low grade: mix of tubular & cribriform pattern
cribriform pattern – Swiss Cheese pattern arranged in a tubular structure
High grade: solid areas of malignant cells
Upper part of the lateral wall of nasal cavity
Types: Papillary, Sessile, Alveolar-mucoid
Surgical resection
C. Malignant melanoma
Mean age : 50 years
Both sexes are equally affected
Presents as slaty-gray / bluish-black polypoidal mass
Anterior nasal septum/MT/IT
Tumour spread by lymphatic & blood stream
Tt : Wide surgical excision
21. D.Olfactory Neuroblastoma( Ethesioneuroblastoma)
Tumour of olfactory placode – neural element of cribiform plate
Both sex at 20-40yr age group
Presents as cherry red, polypoidal mass in upper third of nasal cavity-
nasal obstruction , epistaxis , hyposmia
Cervical node metastasis, multicentre
Local invasion, Systemic spread
Biopsy: Definite diagnosis
CT Scan: Dumbbell mass –
intracranial fossa & upper nasal cavity
Bone destruction , speckled calcification
Surgical excision followed by radiotherapy
Preoperative chemotherapy- Vincristine ,Cyclophosphamide
22. E. Haemangiopericytoma
Tumour of vascular origin
Age group: 60-70 year
Polypoidal mass , bleeds on touch
Arises from Zimmermann
Pericyte cells of capillaries
Tt: Radiotherapy Wide surgical
Excision. 50% recurrence. 10%(M)
Metastasis to lung, liver, bone
23. Malignant Neoplasm of PNS
Maxillary sinus m.c. site
Early clinical features:
Nasal Stuffiness
Blood stained nasal discharge
Facial paraesthesia or pain
Epiphora
Late clinical feature:
Medial spread: u/l nasal obstruction, u/l purulent nasal discharge,
epistaxis, friable, nasal mass
Anterior spread: cheek swelling, invasion of facial skin
Inferior spread: expansion of alveolus with dental pain, loosening of
teeth, poor fitting of dentures, swelling in hard palate or alveolus
Superior spread: Proptosis, diplopia, ocular pain
Posterior spread: Pterygoid muscle involvement- Trismus
Intracranial spread: Ethmoid, cribriform or foramen lacerum
Lymphatic spread: neck node metastasis
Systemic spread: Lungs, bone
24.
25. Diagnosis
Diagnostic Nasal Endoscopy
X-ray PNS: expansion & destruction of
bony wall
CT scan Nose & PNS: with contrast
Biopsy
Ohngren’s Classification
Ohngren’s line:
Imaginary plane extending b/n medial canthus of eye & angle of
mandible.
Supra structural growth: poor prognosis
Infra structural growth: better prognosis
26. Lederman’s Classification:
2 horizontal lines pass through floors of orbits & maxillary sinus:
Supra structure, Mesostructure, Infrastructure
27.
28. Treatment :
T1 and T2 : Surgery or Irradiation
T3 and T4 : Combined modalities
Inoperable tumour : Chemo radiation
Intra-arterial infusion of 5-Fluorouracil or Cisplatin
29. SURGICAL OPTIONS
A. Total Maxillectomy
Weber – Ferguson incision
Malignancy limited to maxilla
B. Radical Maxillectomy with Orbital exenteration
Involvement of orbital fat
C. Anterior Cranio-facial resection
Extended lateral rhinotomy incision
Involvement of cribriform plate , frontal sinus
30. MAXILLECTOMY
TUMORS CONFINED TO LATERAL NASAL WALL
TUMOURS CONFINED TO UPPER ALVEOLUS OR HARD PALATE
TUMORS LIMITED TO ROOF OF THE MAXILLARY SINUS
AND/OR ETHMOID SINUS WITH OR WITHOUT ORBITAL
INVOLVEMENT
TUMOURS CONFINED TO UPPER ALVEOLUS OR HARD PALATE
WITH LIMITED INVOLVEMENT OF LOWER HALF OF MAXILLARY
SINUS/NASAL CAVITY; POSTERIOR EXTENSION( PTERYGOID
PLATE)
INVOLVES REMOVAL OF THE HARD PALATE & THE ORBITAL
FLOOR ALONG WITH THE ENTIRE MAAXILLA ON ONE SIDE OF
THE FACE
31. WEBER FERGUSSON INCISION
Line drawn through the vermillion border along with filtrum of the
lip , extending around the base of the nose & along the facial nasal
groove.
35. Step. 4: Osteotomies
First Bone Cut(1) Malar prominence.Cut is made anterior(1a) or posterior
( 1b1 and 1b2) to the malar prominence acc. to tumour extent.
Second Bone Cut: (2) Palate is transected with Gigli saw through the nose
into the mouth at the junction of hard & soft palate
Third Bone Cut (3): separate naso-maxillary suture extended superiorly to
the level of 2-3mm inferior to a line paralleling the ant. & post.ethmoid vessel
Fourth Bone Cut(4): chisel is turned posteriorly into ethmoid labyrinth to the
depth of PEA & turns inf. to Inferior Orbital fissure
Fifth Bone Cut(5) : Mandible is depressed , pterygoid plates amputated from
skull base/ posterior sinus wall
36. Step.5: Delivering the Maxilla
Maxilla is delivered by antero-inferior traction.
Step.6: Reconstruction & Wound Closure
Reconstruction includes: 1. Dacryocystorhinostomy (DCR)
With lacrimal sac marsupialization
2. Orbital floor reconstruction – titanium mesh/free cartilage/bone graft/
osteocutaneous free micro vascular flaps
ORBITAL EXENTERATION
Tumour invading orbital soft tissues ( lid, lacrimal apparatus, globe,
muscle or fat)
1. Incision
2. Dissecting the Periorbita
3. Transection of Orbital Apex Tissue Bundle
4. Final closure
37. INCISION Dissecting the Periorbita
Transection of Orbital Apex
Tissue Bundle
Final closure. A. Front view, B. saggital
view
38. Anterior Craniofacial Resection
Tumoursinvolving anteriorskull base
Allows wideexposureofthe complexanatomicalstructuresatthe baseofskull permittingmonobloc
tumourresection
Classical cfr : transfacial/ transnasal and trans cranial approach
Modified cfr : endoscopic assisted cfr in place of transfacial approach
39. MIDFACIAL DEGLOVING
Advantage – 1. very good exposure
2. bilateral exposure
3. less post operative complication
4. can be combined with CFR
5. cosmetic results
Tumours resectable:
1. Inverted papilloma
2. Squamous cell carcinoma
3. Angiofibroma
4. Haemangioma
5. Plasmacytoma
6. Ameloblastoma
40. 3 steps
A. Bilateral maxillary vestibular approach & Sub periosteal dissection- by
bilateral sub labial incision from maxilary tuberosity to tuberosity
41. B. Circular endonasal incision using
Inter-cartilaginous incision (A)
Transfixion incision (B)
Incision of the nasal floor along the piriform aperture
42. C. Degloving of the nose, nasal radix & ethmoid region
Area exposed: Nasal cavity, nasopharynx , maxillary
antrum , ethmoid, sphenoid, skull base .
45. Step2 : Removal of the Uncinate & identification of natural
ostium
Step 3: Identification of Hasner Valve
46. Step 4: Subtotal Inferior Turbinectomy
Step 5 : Creation of a Nasal Floor Mucosal Flap
47. Step 6 : Mega –antrostomy
Step 7: Exposure of the Anterior, Inferior or Lateral
Maxillary sinus ( when necessary)
48. Step 8: Removal of the Tumour Pedicle
Postoperative Considerations
Irrigation with saline solution
Serial in office debridement
Patient should be instructed to massage the NLD in postoperative
period
Long term surveillance for recurrence