Bayan Al Othman, MD, Claudia Prospero Ponce, MD, Jonathan Austin Go, Randy Igbinoba, MD, MPH, MBA, Vannessa Leung, MD, Aroucha Vickers, DO, Claudia Prospero Ponce, MD, Ashwini Kini, MD Show
Assigned status Up to Date by Claudia Prospero Ponce, MD on August 7, 2022. Disease EntitySuperior orbital fissure syndrome (also known as Rochen-Duvigneaud syndrome) DiseaseSuperior orbital fissure syndrome (also known as Rochen-Duvigneaud syndrome) is a collection of symptoms caused by compression of structures just anterior to the orbital apex [1]. The complex and crowded anatomy of the superior orbital fissure produces a characteristic pattern of cranial nerve, pupillary and extraocular findings. Importantly the optic nerve is spared which differentiates superior orbital fissure syndrome from orbital apex syndrome [2] . This constellation of findings was first described by Hirschfeld in 1858 and officially named by Rochen-Duvigneaud in 1896 [3]. EtiologySuperior orbital fissure syndrome is rare, and the majority of literature consists of case reports and case series. When originally identified, the syndrome was thought to be secondary to a “syphilitic periostitis” [4] because it responded when treated for syphilis. The most frequent cause of superior orbital fissure syndrome is now known to be trauma, which is seen in 0.3-0.8% of patients [3][5] [6] . Common associations are motorcycle accidents, zygomatic fractures and orbital fractures [7] . Trauma-related superior orbital fissure syndrome often presents within 48 hours of a facial injury, but presentation can also be delayed by several days [8] . Other causes include neoplasms (particularly lymphoma and rhabdomyosarcoma) [9] , infections (such as meningitis) [10] , syphilis [11] , sinusitis [12] [13] , herpes zoster [14] [15] [16] , inflammation (such as Lupus, sarcoidosis, Tolosa-Hunt syndrome) [2] and vascular phenomena (such as carotid-cavernous fistulas, retro-orbital haematoma and carotid aneurysms), [5] [17] or idiopathic.[18] Rarely, superior orbital fissure syndrome has presented perioperatively in orbital hypertelorism surgery [19] . Presentation from trigeminocardiac reflex episodes during skull base surgery has also been reported [20]. Risk FactorsThe only reported risk factor for superior orbital fissure syndrome is a pre-existing narrow superior orbital fissure [5]. AnatomyImage 1: View of orbital apex, right orbit. The tendon of the lateral rectus muscle divides the fissure into two parts: superior and inferior. The ophthalmic artery enters the orbit through the optic canal, whereas the superior and inferior divisions of cranial nerve (CN) III, CN VI, and the nasociliary nerve enter the muscle cone through the oculomotor foramen. CN IV, the frontal and lacrimal nerves, and the ophthalmic vein enter through the superior orbital fissure and thus lie within the periorbita but outside the muscle cone. Note that the presence of many nerves and arteries along the lateral side of the optic nerve mandates a superonasal surgical approach to the optic nerve in the orbital apex. © 2018American Academy of Ophthalmology. http://www.aao.org. Orbital roof, showing Superior orbital fissure. Available at AAO website, accessed on 8/7/22. The superior orbital fissure is a bony cleft found at the orbital apex between the roof and lateral wall. It is a communication between the orbital cavity and middle cranial fossa and is bounded by the greater wing, lesser wing and body of sphenoid [21]. Its dimensions are 22mm in length and 2-8mm in width (narrowest and widest parts) and it is pear-shaped with a wide base nasally on the body of sphenoid and an apex directed superotemporally[5]. There is no significant variation of SOF size between gender or body type.[22] Anteriorly the superior orbital fissure is related to the annulus of Zinn (common tendinous ring) on which the four rectus muscles attach. The annulus splits the superior orbital fissure into three sectors: lateral, central (oculomotor foramen) and inferior. The lateral sector contains the lacrimal, frontal and trochlear nerves and superior ophthalmic vein. The central sector, which is surrounded by the annulus of Zinn, contains the superior and inferior branches of oculomotor nerve, nasociliary and abducens nerves. The inferior sector contains the inferior ophthalmic vein[21][23] [24]. Older literature divided the superior orbital fissure into two (superior and inferior) divisions, rather than three, though the relative location of the contents inside superior orbital fissure has remained consistent[25]. PathophysiologyCompression of structures in superior orbital fissure syndrome can be attributed to a bony fragment (such as with facial fractures) or mass effect. In all causes of superior orbital fissure syndrome, inflammation and compression of nearby nervous tissue is responsible for the majority of clinical symptoms.[18] Since the orbital muscle cone is of relatively fixed volume, being bounded by the intermuscular membrane and Tenon’s capsule, any edema or bleeding or masses in this area compromises delicate neural structure [26].
DiagnosisClinical PresentationThe common clinical findings in superior orbital fissure syndrome include the following and their individual anatomical basis are explained [5][16]
Diagnostic ProceduresThe diagnosis of superior orbital fissure syndrome is suspected on clinical grounds. Imaging studies play a role in confirming the diagnosis, and more importantly, give insight into underlying etiology. Early use of plain film with superior orbital fissure views (20-25° head tilt) has largely been replaced by widespread availability of CT and MRI. The most common imaging modality is currently CT with 2mm fine cuts looking for bony fragments or compressive masses. Where a vascular cause is suspected, angiography is recommended to define any carotid-cavernous fistula or carotid aneurysm [5]. In cases managed conservatively or medically there is little consensus on need for follow-up imaging but Shama et al. (2012) suggests a repeat MRI at 6 months [1]. Differential DiagnosisImportant differentials to distinguish from superior orbital fissure syndrome are as follow (see Table 1):
Table 1: Differentials for common misdiagnoses of superior orbital fissure syndrome ManagementThe management of superior orbital fissure syndrome depends on its etiology. Treatment is not standardized because relatively few cases have been documented. Reported treatment options include medical and surgical intervention, as well as observation alone [35]. Indications for urgent intervention are vascular causes (requiring embolization) and bony fractures with displaced fragments or severe foraminal narrowing [3], particularly lateral orbital wall fractures [36]. Cases involving neoplasms, physical impingement, infections, or retrobulbar hemorrhage warrant the use of surgical exploration.[18] In certain cases, a combination of treatment options may be appropriate, such as a megadose corticosteroid treatment combined with surgical intervention [36]. FracturesIf the superior orbital fissure is compressed or narrowed by a facture, surgical decompression may be beneficial [35][36]. Surgical management in the non-urgent setting is performed at an average of 10.7 days due to concerns that early intervention is associated with increased swelling and ocular pressure [3]. Both orbital and cranial extradural approaches have been described including extranasal intraorbital to access the lateral wall, extranasal transethomoidal to access the medial wall, a modified extranasal intraorbital route, transtemporal route in causes of infectious collections and combined orbital and cranial for deep decompressions [37][38][39]. An endoscopic transmaxillary transMuller’s muscle route for decompression may also be effective, though sample size is limited [40]. A concomitant facial fracture can be surgically reduced [35]. EdemaHistorical treatment of restricted movement due to edema has focused on conservative management and careful observation because spontaneous improvement had been documented in the past. However, if there is no evidence of bone dislocation, and thus no need for urgent surgical intervention, conservative medical treatment involving megadoses of corticosteroids has proven effective [35][36]. The most common regimen mirrors that of spinal cord/nerve injury protocols and involves intravenous IV methylprednisolone as a 30mg/kg bolus followed by a 5.4mg/kg/h on a 48 hour infusion, followed by oral prednisone taper over 2 weeks [4][41]. VascularIn cases of retroorbital hematoma, hemorrhage generally resorbs spontaneously after 3-12 weeks. However, some authors recommend intervention if the hematoma is associated with fractures, such as aspiration, open reduction, or intravenous steroids [35]. Cases of carotid-cavernous sinus fistula can be confirmed with carotid angiography and treated via detachable balloon or coil embolization [35]. Conservative TreatmentConservative treatment through observation alone has been suggested due to the operative difficulty and risk of further injury from surgical exploration. Spontaneous recovery, both complete and partial, of motor and sensory function has been reported in cases of traumatic etiology [42]. A recent literature review documented nineteen cases of superior orbital fissure syndrome secondary to craniofacial trauma treated with observation alone, with complete spontaneous recovery in eight of the cases [35]. Complications and PrognosisNo adverse effects from medical therapy with high dose steroids in this setting have been described [34]. Complete recovery of all nerves has been reported in 24-40% of patients receiving steroid treatment compared to 21.4% in those without. Recovery is usually extended over a period of months with progress plateauing at 6 months. The abducens nerve which is most commonly damaged shows the best recovery. Possible sequelae from superior orbital fissure syndrome may include remaining deficit requiring further strabismus or ptosis surgery[3] [5] References
The Academy uses cookies to analyze performance and provide relevant personalized content to users of our website. Which projection will best demonstrate orbital floor fracture?study for review class. Which cranial bone is affected by mastoiditis quizlet?The mastoid is a division of the temporal bone, which forms portions of the side and base of the skull.
Which positioning line is placed perpendicular to the IR for the Parieto orbital oblique?Which positioning line is placed perpendicular to the IR for the parieto-orbital oblique projection of the optic foramina? The proper name for the parieto-orbital oblique projection is the Schuller method. Optic foramen studies are routinely taken as bilateral projections.
Which cranial bone contains the foramen ovale quizlet?The foramen magnum is the large opening at the base of the occipital bone; the foramen rotundum, foramen ovale, foramen spinosum, & optic foramen are small openings found in the greater wings of the sphenoid bone.
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