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6 Rhinology
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• Foreign bodies (local irritation or secondary to attempts at removal).
• Tumors (secondary to erosion into vessels).
• Carotid aneurysm (rare, usually a late complication occurring several
Systemic.
• TB, Wegener’s granulomatosis (respiratory tract granulomas, vasculitis,
• Hypertension—association between epistaxis and hypertension is con-
• Hereditary hemorrhagic telangiectasia.
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years after trauma accompanied by monocular blindness).
and glomerulonephritis), sarcoidosis (noncaseating granulomas), syphilis.
– Symptoms=crusting, friable mucosa, septal perforation.
troversial; recent systematic review and meta-analysis did support this association.
– Autosomal dominant, numerous small vascular malformations of the
skin and mucosal linings of the aerodigestive tract, AVMs of larger organs (lung, liver, brain).
– Epistaxis and GI bleeding common, onset at puberty and worsens
with age. – Lack of normal vascular smooth muscle, impairs ability to contract. – Treated with bipolar cautery or laser ablation, septodermoplasty, or
nasal closure as a last resort. – Use of bevacizumab (Avastin), a VEGF inhibitor, has had increasing
use as an intranasal injection.
Blood dyscrasias.
• Thrombocytopenia which has a broad differential diagnosis and can be classied by a production, destruction, or redistribution problem.
• Alcoholism, malnutrition, malignancy, immunodeciency, liver or kid­ney failure.
– Characterized by reduced platelet aggregation, prolonged bleeding
time; treat with platelet transfusion for severe bleeds.
• von Willebrand disease.
– Deciency of von Willebrand protein leads to defective platelet adhe-
sion and decreased activity of clotting factor VIII; treat with DDAVP, cryoprecipitate, or von Willebrand protein concentrate for severe bleeds.
• Hemophilia.
– Deciency in clotting factor VIII (type A) or IX (type B); treat with
factor VIII or IX concentrate.
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K. Phillips et al.
• Drugs (i.e., NSAIDs, anticoagulants).
– NSAIDs, ASA, and clopidogrel characterized by reduced platelet
function; treat with platelet transfusion.
– Coumadin inhibits formation of multiple clotting factors; reverse
with vitamin K and FFP.
– Other anticoagulants include heparin, enoxaparin, rivaroxaban, dabi-
gatran, apixaban, edoxaban, and fondaparinux, whose all mecha­nisms of action target the clotting cascade at different levels.
– Management: Determine acuity, and remember ABCs; ensure patient is sta-
ble, and address any systemic disease or obvious associated comorbidity.
Topical vasoconstriction (e.g., oxymetazoline) and manual pressure at the lower 1/3 of the nose for minor bleeds. Cauterization (silver nitrate, electric, or KTP/argon laser). Nasal packing can be absorbable or non-absorbable and can place pres­sure either anteriorly or posteriorly, ranging from a variety of nasal tam­pon devices to Vaseline gauze packing to absorbable hemostatic materials.
• Absorbable packing:
– Does not necessarily need to be removed. – Useful in patients on anticoagulation, with thrombocytopenia, or
other blood dyscrasias or in other systemic illness predisposing to epistaxis
• Anterior packing:
– Removed after 2–5days, depending on severity and etiology – Can be managed outpatient unless patient is frail or has underlying
coagulopathy, which requires treatment
– Complications: toxic shock syndrome (give anti-staphylococcal anti-
biotic while packing in place), sinusitis from blockage of sinus ostia, septal necrosis/perforation
• Posterior packing:
– Often requires sedation due to discomfort. – Requires inpatient stay to monitor airway; elderly or frail patients
and those with underlying cardiopulmonary disease should be moni­tored in intensive care unit with low threshold for intubation.
– Complications: airway compromise, nasal-vagal reex (hypotension
and bradycardia), alar necrosis.
Greater palatine foramen injection (local anesthetic 1% lidocaine 1:100,000 epinephrine inltrated into foramen—must aspirate prior to injection to ensure not in the vessel) helps control posterior bleeds. Surgical evaluation with ligation of bleeding vessel(s):
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• Internal maxillary artery (IMA): open posterior maxillary sinus wall;
• Sphenopalatine artery (SPA): endoscopically dissect in a subperiosteal
• Anterior/posterior ethmoid arteries (AEA/PEA): can either identify
Angiography and embolization:
• Angiography identies site of active bleed; interventional radiologist
• Complications: blindness (more common with internal carotid branches,
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identify branches of IMA in pterygopalatine foramen and ligate with clips.
plane along the medial inferior maxillary wall just anterior to lamellar attachment of middle turbinate; identify SPA as it exits at crista ethmo­idalis, and ligate with clip or cauterize.
endoscopically and cauterize with bipolar cautery within the nasal cav­ity or perform Lynch incision and dissect periorbita off medial orbital wall; AEA located 8–12mm from lacrimal crest, PEA 10–12mm from AEA, and optic nerve 4–6mm from PEA.
performs embolization of specic branch or branches of external carotid.
and embolization of these branches would only be undertaken in a life­saving procedure), necrosis, stroke, facial pain, paresthesia.
Benign Masses/Abnormalities
• Nasopharyngeal cysts
– Rathke’s pouch cyst or craniopharyngioma
Remnant of ectodermal tissue precursor of anterior pituitary gland Tx=reassurance versus endoscopic marsupialization if symptomatic
– Tornwaldt cyst
Remnant of caudal notochord Tx=reassurance versus endoscopic marsupialization if symptomatic
• Midline nasal masses
– Arise as a result of failure of closure of anterior nasopore – Persistence of fonticulus frontalis (opening between nasal and frontal bones
in the embryo) allows for intracranial connection to prenasal space – MRI=allows for assessment of intracranial extension (IC) – Biopsy of midline nasal mass in children contraindicated due to risk of IC
extension – Tx = open vs. endoscopic surgical excision, depending on whether or not
external nasal structures involved – Glioma
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60% Extranasal, 30% intranasal, 10% combined “Pinched off” glial tissue; can appear red and be confused with hemangioma Symptoms=rm, nontender, noncompressible mass that does not transil­luminate or change in size
– Encephalocele, meningocele, meningoencephalocele
Herniation of meninges (meningocele), meninges + brain (meningoen­cephalocele), or meninges+brain+part of ventricular system (meningo­encephalocytocele) through skull base defect. Sac of glial tissue lined with ependymal cells. 25% Anterior (sincipital/external versus basal/internal) and 75% posterior, or occipital inlocation.
• Sincipital/external: herniation occurs anterior to crista galli between frontal and ethmoid bones, presenting as external mass over nose or glabella.
• Basal/internal (less common): herniation occurs posterior to cribriform plate, presenting as an intranasal mass.
Symptoms: soft, compressible mass that transilluminates and increases in size with crying (positive Furstenberg test)
– Dermoid Cyst
K. Phillips et al.
Sequestration of ectodermal and mesodermal elements anywhere along a tract extending from foramen cecum to nasal tip Symptoms=Fistulous tract, nasal pit with tuft of hair
– Fibro-osseous lesions (nd also in Systemic Diseases chapter)
Osteoma=most common benign sinonasal lesion
• Frontal sinus most common
• Gardner’s syndrome = skull osteomas, colonic polyps, and soft tis­sue tumors
Fibrous dysplasia
• Two types: Monostotic (most common, 70–80%) and polyostotic
McCune-Albright syndrome=polyostotic lesions, precocious puberty, pigmented skin lesions
• CT ndings: Early = radiolucent; Late = “ground glass”+calcications
• Tx=surgery only if symptomatic (debilitating pain or cosmetic defor­mity effecting quality of life), bisphosphonates
Ossifying broma
• Solitary encapsulated slow-growing monostotic tumor
• CT ndings=central lucency with eggshell rim
• Tx=surgery
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Aneurysmal bone cyst
• Often seen in rst and second decades of life
• Osteolytic lesion consisting of blood-lled spaces separated by osteoid tissue and containing osteoclast giant cells
– Cerebrospinal uid (CSF) rhinorrhea, may be associated with encephaloceles
or other midline nasal masses
Can present with unilateral rhinorrhea, postnasal drip, metallic or salty taste, pulsatile tinnitus, headaches, balance disturbance, visual change, headaches, or history of recurrent meningitis. Workup includes testing of rhinorrhea for beta-2 transferrin positivity and imaging of the skull base (thin-cut CT to evaluate for bony dehiscence, thinning, or scalloping of the skull base and MRI to evaluate for encepha­locele and associated intracranial ndings of elevated intracranial pres­sure) and may need CT cisternogram for occult cases. Classied into four categories, congenital, traumatic/iatrogenic, neoplas­tic, or spontaneous:
• Congenital CSF leaks are often associated with malformations or the meningoencephalocele spectrum; repair is dictated by location and par­ticular local expertise of treating otolaryngologist and neurosurgeon.
• Traumatic CSF leaks complicates 2% of head trauma and 12–30% of basilar skull fractures; can be treated conservatively with strict bedrest, head-of-bed elevation, restriction of straining with the aid of antiemet­ics and stool softeners, and CSF diversion procedures. If the leak fails to respond to conservative management or depending on clinical status, it can be repaired either endoscopically or open (techniques described below in the “Major Complications of Sinus Surgery” section).
• Iatrogenic CSF leaks are often repaired at time of injury and are described below in the “Major Complications of Sinus Surgery” section.
• Neoplastic CSF leaks are managed in the context of malignancy.
• Idiopathic CSF leaks are often associated with idiopathic intracranial hypertension (IIH) and present spontaneously; more common in obese middle-aged women; associated ndings on imaging include broadly attenuated or scalloping of the skull base, arachnoid pits, multiple skull base defects, or empty sella syndrome. It often requires multidisci­plinary approach including evaluation by otolaryngology, ophthalmol­ogy, neurology, and neurosurgery. Treatment includes repair of skull base defect (techniques described below) and then possible trial of acet­azolamide (carbonic anhydrase inhibitor), weight loss, bariatric surgery, or CSF diversion techniques depending on the clinical situation.
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– Inverted papilloma—most common benign epithelial tumor of the nose and
paranasal sinuses
Arises from the Schneiderian membrane (transition between the endoderm­derived respiratory epithelium and the ectoderm-derived squamous epithe­lium), association with HPV (usually types 6 and 11).
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Histologically, the epithelium inverts into underlying stroma but does not cross the basement membrane. Appears as a unilateral exophytic pink to tan mass. Most common sites of attachment include the lateral nasal wall and maxil­lary sinus (may see bony thickening at site of attachment on CT). Can be locally destructive with tendency to reoccur and associated 10% malignancy rate and therefore treated with aggressive surgical resection with close surveillance after resection. In addition to inverted papilloma, other intranasal papillomas arising from the Schneiderian membrane include fungiform/exophytic papillomas (most commonly on nasal septum) and oncocytic/cylindrical papillomas.
– Antrochonal polyp
Benign unilateral lesion arising from a cyst in the maxillary sinus growing into the nasal cavity to the choana, often presenting with nasal obstruction Treatment with surgical resection including attachment site in the maxil­lary sinus to prevent reoccurrence
– Vascular lesions
Hemangioma—often along septum or inferior turbinate, present with epi­staxis; if symptomatic, treat surgically (+/ perioperative embolization); can be associated with pregnancy and should be treated conservatively in pregnancy if able Hamartomas
K. Phillips et al.
• Respiratory epithelial adenomatoid hamartoma, which often originates in the olfactory cleft; can be associated with nasal polyposis
• Seromucinous hamartoma, which shows haphazard proliferation of seromucinous glands
Sinonasal Malignancy
See Head and Neck chapter.
Surgical Approaches
• Endoscopic approach (endoscopic sinus surgery or ESS)
– Technique=Rigid nasal endoscopy+/stereotactic image guidance; typical
steps include medialization of middle turbinate, removal of uncinate process, maxillary antrostomy, ethmoidectomy, sphenoidotomy, and frontal recess exploration with sinosotomy as needed.
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Consider mega-antrostomy or pre-lacrimal approach in patients with cystic brosis, recalcitrant inammatory disease, tumor access, or need for better visualization/monitoring of the maxillary sinus.
– Four lamellae encountered (anterior posterior)=uncinate process eth-
moid bulla vertical portion of middle turbinate basal lamella vertical portion of superior turbinate basal lamella.
– Should be considered for any lesion or disease process (congenital, inamma-
tory, neoplastic, traumatic, etc.), which can be accessed endoscopically, but the rhinologic surgeon must be familiar with open approaches for lesions that are inaccessible or incompletely addressed via this approach.
– Complications=bleeding, synechiae, injury to the eye including blindness,
CSF leak, nasolacrimal duct injury, hyposmia, and brain injury.
– Specic endoscopic approaches to the frontal sinus:
Draf I: complete removal of the anterior ethmoid cells and uncinate pro­cess within the frontal recess leading to the frontal ostium. Obstructing frontal cells, if present, are removed. The frontal sinus ostium may then drain into a patent frontal recess, but the frontal sinus ostium itself is not instrumented. Draf IIa: resecting all included in Draf I with the addition of widening the frontal sinus ostium itself, resecting all of the frontal sinus oor from lam­ina to the insertion of the middle turbinate medially. Draf IIb: resecting all included in Draf IIa with the addition of resecting the middle turbinate up to skull base and widening the frontal sinus medi­ally to the septum. Draf III (aka modied Lothrop): resecting all included in Draf II, with the addition of a superior anterior septectomy, removing the intersinus septum, and connecting bilateral frontal sinuses into one horseshoe-shaped sinus with a common drainage pathway.
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– Specic endoscopic approaches to the maxillary sinus:
Medial maxillectomy (aka mega-antrostomy).
• Indications include intractable maxillary sinus inammatory disease, benign tumors of the maxillary sinus, maxillary sinus malignancies that have not invaded into surrounding soft tissue, and access to the pterygo­palatine fossa, infratemporal fossa, and middle cranial fossa.
• Steps include maxillary antrostomy, identication of Hasner valve, and resection of the posterior 2/3 of the inferior turbinate just posterior to the valve (unless the nasolacrimal duct is involved in which case a dac­ryocystorhinostomy would also be indicated) and of the medial wall of the maxillary sinus until nasal oor is ushed.
• For anterior/lateral maxillary sinus access, other modications may be needed (pre-lacrimal approach).
• If there is ethmoid involvement, the lamina papyracea may need to be removed with care to leave the periorbital intact.
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– Specic endoscopic approaches to the ventral skull base:
Transphenoidal
• Indications—approach to lesions within clivus, sella, tuberculum, or planum, e.g., pituitary lesions, meningomas, Rathke’s cleft cyst, craniopharyngiomas.
• Steps include lateralization of turbinates, bilateral sphenoidectomy, posterior septectomy, preservation of bilateral rescue aps, creating common sphenoid cavity by taking down the rostrum, and expanding the opening to visualize bilateral optico-carotid recess as well as other landmarks depending on the level and size of the lesion.
Transpterygoid
• Indications—endonasal access to the lateral recess of the sphenoid sinus, middle cranial fossa (petrous apex, Meckel’s cave, cavernous sinus), infratemporal fossa, or the eustachian tube and nasopharynx.
• Steps include raising the contralateral nasoseptal ap if a CSF leak is anticipated or possible (as the ipsilateral SPA will likely be sacri­ced), ranssphenoidal approach, modied medial maxillectomy, removal of the posterior wall of the maxillary sinus with care to leave the posterior periosteum intact to prevent spilling the fat of the PPF, ligation of SPA, retraction of PPF contents, and inferior and lat­eral+/removal of the pterygoid plates depending on specic region needed for access.
K. Phillips et al.
Transclival
• Indication—endonasal access to clivus, posterior cranial fossa; same anterior approach as for nasopharyngectomy.
• Steps include inferior posterior septectomy, drilling down of maxillary crest, identication of medial pterygoid plates, and identication of where eustachian tubes may need to be transected. Finding buccopharyngeal and pharyngobasilar fascia, either using to create a plane or transecting to move past to skull base. For posterior cranial fossa, approaches involving the upper cervical spine may need to con­sider C-spine xation rst.
Open Approaches
• Caldwell Luc
– Used most often to gain access to the anterior wall of the maxillary sinus – Performed through canine fossa with incision at gingivobuccal sulcus
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– Can augment endoscopic surgery; good for anteriorly attached IP or other
tumors, broader access to orbital oor and PPF
– Complications = cheek edema/ecchymosis, numbness or pain with infraor-
bital nerve injury, oroantral stula, epiphora if damage to nasolacrimal duct
• External ethmoidectomy
– Provides access to ethmoid cavity, medial orbit, cribriform plate, and fronto-
nasal area if endoscopy is not an option; can be employed to decompress subperiosteal abscess
– Complications=eye injury including blindness and corneal abrasions, CSF
leak, skull base injury, bleeding from AEA+/retraction of vessel into the eye
• External frontoethmoidectomy (Lynch procedure) or frontal trephine
– Indications: uncommonly used now, when endoscopic approach is for any
reason insufcient to address frontoethmoid mucocele, mucopyocele, rhino­sinusitis with orbital complications, frontoethmoid or anterior skull base tumor, CSF leak repair, acute sinusitis with intracranial or orbital complica­tions or not responsive to medical management and unable to access endo­scopically, lateral frontal mucocele
– Complications = bleeding, epiphora, frontal sinusitis, diplopia, blindness,
CSF leak, intracranial hemorrhage
• Osteoplastic ap with frontal sinus obliteration or cranialization
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– Indications = when endoscopic approaches are insufcient or have failed to
address osteomyelitis, mucocele, frontal sinus tumor, osteoma, recurrent persis­tent frontal sinusitis, trauma with comminuted anterior or posterior table fractures
• Open approaches to sphenoid sinus (historically used by neurosurgeons in pitu­itary surgery)
– Transseptal: incision can be endonasal, sublabial, or transcolumellar
• Transfacial incisions
– Lateral rhinotomy (incision made in naso-facial crease for small lesions of
nasal cavity and medial maxilla), historically used for IP, no longer “gold standard”
– Weber-Ferguson (incision for lateral rhinotomy extended laterally in subcili-
ary crease and inferiorly along philtrum through vermilion border to split lip, provides wide access for most sinonasal tumors)
• Craniofacial resection
– Bifrontal craniotomy with transfacial exposure of sinonasal cavity and orbits,
allows for access to anterior cranial fossa
– Used to approach skull base pathology including malignancy that cannot, for
whatever reason, be accessed via the endoscopic approach
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K. Phillips et al.
Major Complications ofSinus Surgery
• Orbital
– Includes blindness (direct injury or hematoma), penetration of orbit (may see
fat herniation), diplopia (muscle injury—often medial rectus or superior oblique muscle), and epiphora (damage to lacrimal system).
– Retrobulbar hematoma is an acute complication which must be recognized
immediately and treated to avoid blindness.
Cause = most commonly from venous injury near lamina papyracea or arterial injury to AEA during endoscopic surgery retraction of vessel into orbit where pressure from hematoma compresses optic nerve. Sx=proptosis, chemosis, ecchymosis, and vision change (if awake). Treatment = immediate ophthalmology consult; ice packs; mannitol; remove any nasal packing if it has been placed; surgical intervention (lat­eral canthotomy+/medial orbital wall decompression). Prevention=keep eyes visible during surgery, and evaluate any imaging preoperatively to identify AEAs which run below skull base.
• Major vascular injury to carotid artery
– Place enough pressure with pledgets to staunch blood ow but not compress
artery fully, preserving blood ow to the brain. – Can harvest muscle patch, crush and place to repair minor injuries. – Regardless of whether muscle patch is placed, patient needs to then undergo
interventional angiography to evaluate the vessel and branches.
• CSF leak.
– If identied at the time of surgery, the defect should be repaired at that time
(most common site of iatrogenic injury = lateral lamella of ethmoid roof)
depending on surgeon comfort or immediate referral to rhinologist. – If identied postoperatively (beta-2 transferrin positive thin watery rhinor-
rhea) conservative management can be tried rst, although many surgeons
would opt to go straight to surgery for repair. – Conservative treatment=7–10days of bed rest, head elevation, stool soften-
ers to avoid straining, and lumbar drain for diversion (+/ antibiotics (pro-
phylaxis for meningitis)—no evidence to support use; however most continue
to use). – Surgical repair:
Intracranial approach (50–70% success rate) requires a coronal approach and carries risks of frontal lobe dysfunction, cerebral edema, seizures, and anosmia. Extracranial approach (80% success rate) uses transfacial incisions, pro­viding better visualization of the site of CSF leak but resulting in facial scarring.