- •Chapter 1
- •Ocular Adnexal Lymphoproliferative
- •1.1 Pathogenesis
- •1.2 Chronic Antigen Stimulation
- •1.3 Immunosuppression
- •1.4 Pathology
- •1.5 Cytogenetics
- •1.6 Clinical Features
- •1.7 Imaging Findings
- •1.8 Staging
- •1.9 Positron Emission Tomography
- •1.10 Treatment
- •1.11 Follicular Lymphoma
- •1.12 Mantle Cell Lymphoma
- •1.13 Radiotherapy
- •1.14 Chemotherapy
- •1.15 Immunotherapy
- •1.16 Radioimmunotherapy
- •1.17 Outcome
- •1.18 The Future
- •References
- •Chapter 2
- •2.1 General Introduction
- •2.2 The Aging Process and Facial Analysis
- •2.3 Endoscopic Brow Lift
- •2.3.1 Introduction
- •2.3.2 Endoscopic Browlift Anesthesia Pearls
- •2.3.4 Endoscopic Browlift Postoperative Care Pearls
- •2.4 Upper Blepharoplasty
- •2.4.1 Introduction
- •2.4.2 Patient Evaluation
- •2.4.3 Upper Blepharoplasty Anesthesia Pearls
- •2.4.4 Upper Blepharoplasty Surgical Procedure Pearls
- •2.5 Lower Blepharoplasty, Fillers, and Midface Augmentation
- •2.5.1 Introduction
- •2.5.2 Patient Evaluation
- •2.5.3 Lower Blepharoplasty Anesthesia Pearls
- •2.5.4 Lower Blepharoplasty Surgical Procedure Pearls
- •References
- •Chapter 3
- •3.1 Introduction
- •3.2 What Is the Diagnosis?
- •3.2.1 Pitfalls of Diagnosis
- •3.2.2 A Diagnostic Corticosteroid Trial?
- •3.2.3 The Question of Biopsy
- •3.3 Treatment
- •3.3.1 Corticosteroids
- •3.3.2 Radiation
- •3.3.3 Other Agents
- •3.4 Special Circumstances
- •3.4.1 Pediatric IOIS
- •3.4.2 Sclerosing Pseudotumor
- •3.4.3 Tolosa–Hunt Syndrome
- •References
- •Chapter 4
- •4.1 Introduction
- •4.2 Embryology, Anatomy, Physiology, and Pathophysiology of the Canalicular System
- •4.3 Infective Causes
- •4.3.1 Periocular Herpes Simplex Infection
- •4.3.2 Bacterial Canaliculitis
- •4.4.1 Lichen Planus
- •4.4.2 Ocular Cicatricial Pemphigoid
- •4.5 Iatrogenic Causes
- •4.5.1 Systemic Drugs
- •4.5.1.2 Docetaxel (Taxotere)
- •4.5.2 Radiotherapy
- •4.5.3 Topical Ophthalmic Treatments
- •4.5.3.2 Mitomycin C (MMC) Therapy
- •4.5.4 Lacrimal Stents and Plugs
- •4.6 The Surgical Approach to Managing Canalicular Disease
- •4.6.1 Surgical Technique for Dacryocystorhinostomy with Retrograde Canaliculostomy
- •References
- •Chapter 5
- •5.1 Introduction
- •5.2 Nomenclature
- •5.3 Clinical Manifestations of NF1
- •5.4 Orbitofacial Tumors in NF1
- •5.4.2 Malignant Peripheral Nerve Sheath Tumors
- •5.4.3 Optic Pathway Gliomas
- •5.5 Genetics
- •5.5.1 The NF1 Gene
- •5.5.2 Overlapping NF1-Like Phenotype (SPRED1)
- •5.6.1 Introduction
- •5.7 Surgical Management of Orbitofacial Tumors in NF1
- •5.7.1 Introduction
- •5.7.2 Timing of Surgery
- •5.7.3 Periorbital Involvement
- •5.7.3.1 The Upper Eyelid
- •5.7.3.2 The Lower Eyelid and Midface
- •5.7.4 Orbital Involvement
- •5.7.4.1 Proptosis
- •5.7.4.3 Proptosis Due to Optic Nerve Glioma
- •5.7.4.4 Orbital Enlargement with Dystopia and Hypoglobus
- •5.8 The Natural History of NF1 Tumor Growth from Birth to Senescence
- •References
- •Chapter 6
- •6.1 Introduction
- •6.2 Surgical Anatomy of the Lacrimal Drainage System
- •6.3 Basic Diagnostics for Disorders of the Lacrimal Drainage System
- •6.4 Selective Lacrimal Sac Biopsy in External Dacryocystorhinostomy
- •6.5.1 Case A
- •6.5.2 Case B
- •6.5.3 Case C
- •6.5.4 Case D
- •6.5.5 Case E
- •6.5.6 Case F
- •6.5.7 Case G
- •References
- •Chapter 7
- •7.1 Introduction
- •7.2 Patients and Methods
- •7.2.1 Patients
- •7.2.2 Examination
- •7.3 Results
- •7.3.1 Patient Data
- •7.3.3 Family History
- •7.3.4 Pregnancy History
- •7.3.5 Birth
- •7.3.6 Associated Systemic and Ocular Diseases
- •7.3.8 Neuroradiological Findings (Brain MRI)
- •7.3.9 Nasolacrimal System Findings
- •7.4 Discussion
- •7.4.1 Patients
- •7.4.2 Obstetric and Family History
- •7.4.3 Associated Pathologies
- •7.4.3.1 Ophthalmological Findings in Unilateral Disease
- •7.4.3.2 Neuroradiological Findings
- •7.4.3.3 Systemic Diseases
- •7.4.3.4 Nasolacrimal Duct Findings
- •7.5 Conclusions
- •References
- •Chapter 8
- •8.1 Introduction
- •8.2 Evaluation of Complicated Ptosis
- •8.2.1 Compensatory Eyebrow Elevation
- •8.2.3 Innervation Patterns of the Frontalis Muscle
- •8.2.4 Checklist of Preoperative Evaluation of Complicated Ptosis
- •8.3 Surgical Technique of Levator Muscle Recession
- •8.3.1 Principle
- •8.3.2 Approach to the Levator
- •8.3.3 Partial Levator Recession
- •8.3.4 Total Levator Recession
- •8.3.6 Undercorrection and Overcorrection
- •8.4 Surgical Technique of Brow Suspension
- •8.4.1 Materials for Brow Suspension
- •8.4.1.1 Nonautogenous Materials
- •8.4.1.2 Autogenous Fascia Lata
- •8.4.2 Our Technique of Harvesting Autogenous Fascia Lata
- •8.4.3 Mechanical Principals of Brow Suspension
- •8.4.4 Upper Lid Approach
- •8.4.5 Fascia Implantation
- •References
- •Chapter 9
- •Modern Concepts in Orbital Imaging
- •9.1 Computerized Tomography
- •9.2 Three-Dimensional Imaging
- •9.3 Magnetic Resonance Imaging
- •9.3.1 The T1 Constant
- •9.3.2 The T2 Constant
- •9.3.3 Creating the MR Image
- •9.4 Imaging of Common Orbital Lesions
- •9.4.1 Adenoid Cystic Carcinoma
- •9.4.2 Cavernous Hemangioma
- •9.4.3 Dermoid Cyst
- •9.4.4 Fibrous Dysplasia
- •9.4.5 Lymphangioma
- •9.4.6 Lymphoma
- •9.4.7 Myositis
- •9.4.8 Optic Nerve Glioma
- •9.4.9 Pseudotumor
- •9.4.10 Rhabdomyosarcoma
- •9.6 Positron Emission Tomography
- •9.7 Orbital Ultrasound
- •9.7.1 Physics and Instrumentation
- •9.7.1.1 Topographic Echography
- •9.7.1.2 Quantitative Echography
- •9.7.1.3 Kinetic Echography
- •9.7.2 Extraocular Muscles
- •9.7.3 Optic Nerves
- •References
- •Chapter 10
- •10.1 Introduction
- •10.3 Etiology
- •10.4 Microbiology
- •10.5 Changing Pathogens and Resistance
- •10.5.2 Orbital MRSA
- •10.6 Evaluation of Orbital Cellulitis
- •10.7 Medical Treatment of Orbital Cellulitis
- •10.8 Surgical Treatment of Orbital Cellulitis
- •10.9 Prevention of Orbital Cellulitis After Orbital Fracture
- •References
- •Chapter 11
- •11.1 Clinical Picture
- •11.1.1 Clinical Phases
- •11.2 Ocular Complications
- •11.3 Investigation
- •11.3.1 Angiography
- •11.4 Management
- •11.4.1 Active Nonintervention
- •11.4.2 Indications for Treatment
- •11.5 Modalities of Treatment
- •11.5.1 Steroids
- •11.5.1.1 Topical Steroids
- •11.5.1.2 Intralesional Corticosteroid Injection
- •11.5.1.3 Oral Corticosteroids
- •11.5.2 Interferon-Alfa
- •11.5.3 Vincristine
- •11.5.4 Laser
- •11.5.5 Embolization
- •11.5.6 Surgery
- •References
- •Chapter 12
- •12.1 Introduction
- •12.2 Epidemiology
- •12.3 Biological Behavior and Timing of Metastasis
- •12.4 Lateralization
- •12.5 Localization
- •12.6 Clinical Features
- •12.7 Imaging and Patterns of Orbital Metastatic Disease
- •12.8 Biopsy
- •12.9 Common Types of Orbital Metastases
- •12.9.1 Breast Carcinoma
- •12.9.2 Lung Carcinoma
- •12.9.3 Prostatic Cancer
- •12.9.4 Melanoma
- •12.9.5 Carcinoid Tumor
- •12.11 Treatment
- •12.11.1 Radiotherapy
- •12.11.2 Chemotherapy
- •12.11.3 Hormonal Therapy
- •12.11.4 Surgery
- •12.12 Prognosis and Survival
- •References
- •Chapter 13
- •13.1 Introduction
- •13.2 Rituximab
- •13.3 Yttrium-90-Labeled Ibritumomab Tiuxetan
- •13.4 Imatinib Mesylate
- •13.5 Cetuximab
- •References
- •Chapter 14
- •14.1 Introduction
- •14.2 Porous Orbital Implants
- •14.3 Orbital Implant Selection in Adults
- •14.4 Orbital Implant Selection in Children
- •14.5 Volume Considerations in Orbital Implant Selection
- •14.7 Which Wrap to Use
- •14.8 To Peg or Not to Peg Porous Implants
- •14.9 Summary
- •References
- •Chapter 15
- •15.1 Introduction
- •15.2 Etiology and Presentation
- •15.2.1 Etiology of Orbital Volume Loss
- •15.2.2 Etiology of Periorbital Volume Loss
- •15.2.3 Features of Orbital Volume Loss
- •15.2.4 Features of Periorbital Volume Loss
- •15.3 Background to Injectable Soft-Tissue Fillers
- •15.3.1 Historical Perspective on Volume Replacement
- •15.4 Types of Injectable Soft-Tissue Filler
- •15.4.1 Collagen Fillers
- •15.4.2 Hyaluronic acid Fillers
- •15.5 Treatment Areas
- •15.5.1 Orbit
- •15.5.2 Upper Eyelid and Brow
- •15.5.3 Tear Trough
- •15.5.4 Temple and Brow
- •15.6 Other Periorbital Uses of Injectable Soft-Tissue Fillers
- •15.6.1 Upper Eyelid Loading
- •15.6.2 Lower Eyelid Elevation
- •15.6.3 Treatment of Cicatricial Ectropion
- •15.7 Future Developments
- •References
is injected, the needle withdrawn and the filler molded and massaged against the bone to achieve the desired contour and reduce any prominent lumps (Fig. 15.3d). The injections are repeated in successively more lateral locations along the tear trough, by means of serial puncture. Usually 3–5 injections su ce. Care must be taken to avoid placement of more viscous gels, such as Restylane Perlane®, in the pre-septal lower eyelid location, as it is di cult to mold filler here and the very superficial position leads to prominent lumps or blue discoloration and consequent patient dissatisfaction. If additional contouring is required in this area it is best undertaken with a gel of very small particle size, such as Restylane Vittal® or Restylane Touch®, administered via the “haystack” approach. Postoperative recommendations to patients are as for upper eyelid contouring.
In general 1–1.2 ml of filler is su cient for tear trough contouring, but this can range to 3.5 mls when extending out to the malar region [47]. The latter helps to achieve a smoother lower lid/cheek contour and often gives a better esthetic finish. Duration of treatment ranges from 6–18 months although 8–20% of patients will request a touchup prior to this, usually due to insu cient initial fill or patient desire for a fuller look [30, 47].
Bruising and mild swelling is common following teartrough filler treatment and can last up to one week (Fig. 15.3g). However, it is readily camouflaged with concealers or glasses such that less than 20% of patients need to restrict their social engagements or work schedule following treatment [47]. Persistent malar edema has been described with lateral filler placement in a few patients and has proven di cult to treat [30]. Mild lumpiness has been described by up to one third of patients but this usually settles over the next two weeks (Fig. 15.3h). However, it may require additional treatment in up to 15% of cases [30, 47]. This includes further massage by the treating physician, additional filler to smooth out any contor irregularities or dissolution of hyaluronic acid gel. This can be performed in the o ce by injecting 0.2–0.5 ml of a 1500i unit/5 ml solution of hyaluronidase in saline into the lumpy area [47]. The e ects are immediate so the dose of hyaluronidase can be readily titrated against the extent of the lumpiness. Additional filler should not be injected into the treated area for a week to ensure that the e ect of the hyaluronidase has ceased. Blue discoloration has also been reported by 5–10% of patients [30, 47]. It is thought to occur due to a superficial placement of a pool of filler which causes preferential scattering of blue light (Tyndall e ect) or which becomes stained with blood. Treatment for this is also dissolution with hyaluronidase.
Patient satisfaction with lower eyelid/tear trough volume augmentation using hyaluronic acid gel is reported
15.5 Treatment Areas |
223 |
as being in the region of 85%,with 50% of patients expressing “marked” satisfaction with the treatment [30, 47]. Examples of outcomes from tear trough contouring using hyaluronic acid gel (Perlane®) are given in Figs. 15.5a–d.
15.5.4 Temple and Brow
Non-surgical volume augmentation of the temple region with soft-tissue filler is well established for patients with HIV-treatment-associated facial lipoatrophy. In these patients, poly-L-lactic acid (Sculptra®, Dermik Labs, Bridgewater, New Jersey) has been repeatedly used with high patient satisfaction and e ects lasting over three years [11, 41]. However, the use of fillers to treat other causes of temple hollowing remains less well established. Reports are now emerging of the use of injectable softtissue fillers in temple asymmetry following excision of orbitotemporal neurofibromas, as well as in facial aging [52]. Hyaluronic acid fillers have been preferred for treating these causes of temple hollowing as the volume loss is more subtle and requires more careful titration of the dose of filler. The possibility of reversing the treatment, should the patients not like the esthetic result, is also useful. However, a viscous filler, such as Restylane Perlane®, should be selected as the skin overlying the temple is much thicker than the eyelid and can tolerate a filler with a larger particle size. Temple filler should also always be considered in patients receiving lateral upper eyelid/subbrow filler as otherwise the latter can result in a prominent bulge at the lateral brow which contrasts with the adjacent hollow temple.
Patient preparation is as described previously. Injections are given behind the zygomaticofrontal process so as to soften the bony contour of the lateral orbital rim [52]. Care must be taken to avoid the path of the superficial temporal artery. The filler is administered via a serial puncture technique, with 3–5 injections, each delivering approximately 0.3 ml of filler. Placement of the filler is deep within the superficial temporal fascia (Fig. 15.3e). After each aliquot is injected, the filler is massaged and molded against the temporal bone to achieve a smooth contour (Fig. 15.3f).
Typical treatment volumes are 1 ml per side, although this can range up to 3 ml for prominent hollowing following surgical excision (e.g., of a neurofibroma) [52]. As yet, little has been published on the longevity of hyaluronic acid filler in this area but the use of higher viscosity filler and the relative immobility of the skin in that area suggests that e ects may last one year. As with most facial filler treatments, patient satisfaction has been high, with over 80% of patients very or moderately satisfied [52].
224 |
15 Non-surgical Volume Enhancement with Fillers in the Orbit and Periorbital Tissues |
15
a |
b |
c |
d |
e |
f |
g |
h |
Fig. 15.5 Tear trough and temple volume augmentation with injectable soft-tissue fillers. (a) Pretreatment showing tear trough and lateral periorbital hollows. (b) Seven months following injection with Perlane®. (c) Tear trough hollows pre-injection. (d) Eleven months following injection with Perlane®. (e) Right temple hollowing secondary to excision of a neurofibroma. (f) three months following injection of 3ml Perlane® to the right temple. (g) Mild bilateral temple hollowing. (h) Immediately following treatment with Perlane®
Side-e ects of this procedure include transient mild or moderate discomfort which can be associated with chewing,especially if the filler has been placed deep into the temporalis muscle [52]. Localized bruising is also common, although this generally resolves within one week, and occasionally prominence of a temple vein may persist for 2–3 weeks. There is also some initial lumpiness, in keeping with
hyaluronic acid filler treatment in other sites but this soon settles.Alternatively it can be relieved by further massage or additional filler. No patients in the reported series of temple filling with NASHA required dissolution with hyalase although one requested additional filler to one side due to asymmetry [52]. Examples of temple hollowing corrected with injectable soft-tissue fillers are given in Figs. 15.5e–h.
