Journal List > Clin Exp Otorhinolaryngol > v.8(1) > 1158209

Uyar, Kumral, Yıldırım, Kuzdere, Arbağ, Jorayev, Kılıç, and Gümrükçü: Reconstruction of the Orbit With a Temporalis Muscle Flap After Orbital Exenteration

Abstract

Objectives

This study presents the role of the temporalis muscle flap in primary reconstruction after orbital exenteration.

Methods

A retrospective nonrandomized study of orbital exenterations performed between 1990 and 2010 for malignant tumors of the skin, paranasal sinus, and nasal cavity is presented.

Results

The study included 13 patients (nine men, four women; age range, 30-82 years) with paranasal sinus, nasal cavity, or skin carcinomas. Primary reconstruction of the cavity was performed in all patients after orbital exenteration. No visible defects in the muscle flap donor site were present. Local recurrences were readily followed up with nasal endoscopy, whereas radiology helped to diagnose intracranial involvement in three patients. Two patients died of systemic metastases and five died for other reasons

Conclusion

The temporalis muscle flap is readily used to close the defect after orbital exenteration, and does not prevent the detection of recurrence.

INTRODUCTION

Orbital exenteration is the removal of the eyeball and orbital contents [1], and may include the walls of the eyelids and orbital bones. This procedure is disfiguring and destructive. Generally, orbital exenteration is used to treat tumors and, rarely, inflammation and trauma [2,3]. The main reasons for orbital exenteration are tumors originating from the orbital structures, including basal cell, squamous cell, and sebaceous cell carcinomas [4]. In head and neck surgery, orbital exenteration is commonly used to treat skin, nasal cavity, and paranasal sinus malignancies. Orbital exenteration can be further subdivided into total, subtotal, and enlarged types [5].
Postoperatively, orbital exenteration causes aesthetic and psychological problems. Therefore, this procedure is difficult for both patients and doctors. The most important decision is whether to perform primary or secondary reconstruction, as healing of the orbital defect is dependent on the reconstructive method. The goals of reconstruction are to detect recurrent disease, restore the boundaries between the orbit and surrounding cavities, and to produce an acceptable aesthetic outcome.
Several methods are available for reconstructing the defect resulting from exenteration, ranging from cavity healing with granulation tissue to the use of microsurgical flaps to reconstruct the cavity [6,7,8]. In this paper, we describe the use of the temporalis muscle flap to reconstruct the orbital exenteration cavity and discuss the clinical indications for orbital exenteration.

MATERIALS AND METHODS

Subjects

This retrospective nonrandomized study included orbital exenterations performed between 1990 and 2010 to treat malignancies of the skin, paranasal sinus, and nasal cavity with orbital invasion. The age of the patients ranged from 30 to 82 years; nine were men and four were women. The histopathological diagnosis of the tumors, area affected, and complications are summarized in Tables 1, 2, 3, respectively.

Technique

The main concerns stemming from in this procedure are the creation of adequate tumor-free margins and the preservation of as much normal periocular soft tissue as possible for reconstruction. The orbital cavity was repaired with a temporalis muscle flap in all cases. An incision is made from the anterior edge of the tragus to the superior edge of the orbit (Fig. 1C). While avoiding the frontal nerve, the temporoparietal fascia is elevated from the surface of the inner layer with fatty tissue (Fig. 2A). In this manner, the zygomatic arch and lateral orbital wall of the outer surface are exposed. An osteotomy is made in the zygomatic arch. The muscle flap is elevated from the junction of the perichondrium subperiosteally (Fig. 2B). A tunnel is created by drilling in the lateral orbital wall (frontozygomatic rim) (Figs. 2C, 3C). If the eyelid is not included in the specimen, it is sutured to the muscle prepared as the flap (Fig. 3D). If it is resected, a full-thickness skin graft taken from the inguinal area is sutured over the muscle without tension (Fig. 1D). The temporalis muscle is covered by passing it through the tunnel. The edges of the muscle wall are attached to the orbit and the nasal bones (Figs. 1, 3).
Initially, the patients were followed for recurrence with computed tomography (CT). Subsequently, the orbital region and nasal cavity were further examined with endoscopy. Eye prostheses were used in four patients.

RESULTS

The eye was not the origin of the primary tumor in all cases. Histological examinations revealed that the sample included six patients with skin cancers and seven with nasal cavity and paranasal sinus cancers. The most common cancer was squamous cell carcinoma. Of these, four originated in the skin and three in the nasal cavity and paranasal sinuses (Tables 1, 2).
In the orbit, the tumors most frequently involved the periorbital soft tissues (n=13), followed by the anterior compartment of the orbit (n=10).
Paralysis of the frontal branch of the facial nerve was seen in three patients. An orbital fistula developed in two cases. No visible defects were present in the muscle flap donor sites (Table 3).
In our series, four patients had local recurrence. These patients underwent subsequent surgery to close the defect using a midline forehead flap and a cheek flap. These patients were followed for at least 2-5 years. A maxillectomy, ethmoidectomy, or craniofacial resection was performed as necessary. If there was invasion of the orbital wall, the bony structures were also resected en bloc.
Three of the patients died with recurrence involving the skull base and the cavernous sinus of the brain. Recurrences were diagnosed radiologically in these patients. Two patients died of systemic metastases and five died for other reasons (infarction, diabetes complications, and a vehicular accident). Three patients are alive and still being followed.

DISCUSSION

Previously, orbital exenteration was indicated for invasion of the periorbital region; however, it is currently used for tumors invading the orbital apex or sphere.
The decision to perform orbital exenteration when orbital involvement is suspected is difficult. Invasion of the fat and muscles of the orbital apex and infiltration of the conjunctiva or sclera are absolute indications for orbital exenteration.
CT and magnetic resonance imaging (MRI) are not sufficient for a definitive diagnosis of invasion in patients without eye movement limitation and proptosis. Therefore, frozen section examination should be performed during the operation. The tumor histology is important, as exenteration of the orbit is less often necessary in cases of esthesioneuroblastoma, adenocystic low-grade carcinoma and benign tumors, adenocarcinoma, and squamous cell carcinoma [9].
The purpose of the reconstruction is to restore the orbital tissues and to provide an acceptable aesthetic appearance, while allowing fot the detection of recurrent disease.
When considering orbital exenteration, an ophthalmologist, prosthodontist, radiologist, and radiation oncologist should be consulted preoperatively. Patients and relatives should be informed. After these consultations, the surgeon will decide whether to perform primary or secondary reconstruction. Reconstruction methods include temporalis muscle transposition; the use of midline forehead flaps, dermal grafts, dermis fat grafts, and split skin grafts; including globe-sparing exenteration, eyelid-sparing techniques, and spontaneous granulation [9,10].
Primary reconstruction is performed during the initial exenteration operation. It promotes healing, provides a better aesthetic appearance, and enables activities such as bathing, but it can hide recurrences. Postoperative radiotherapy can impair the vascularization of the flap and cause orbital dehiscence [11]. When dural resection and reconstruction are performed in addition to orbital exenteration, primary reconstruction is mandatory in order to avoid the risk of meningitis.
Some surgeons prefer to allow spontaneous healing of the orbital cavity. This approach leads to secretions, mucus retention, and maceration. Sound resonance is worse. However, recurrence can be diagnosed early when the cavity is exposed for secondary reconstruction. The average healing time is 14 weeks, but healing can take up to 6 months [12]. Some case series have found a high rate of sino-orbital fistulas following spontaneous granulation of exenterated orbital cavities (17/25 cases) [7]. Covering the orbit with split-thickness skin grafts and local flaps speeds the healing process. Many regional flaps (temporalis muscle, midline forehead, frontal, or temporo-parietal fascial flaps) or free flaps (rectus abdominis, latissimus dorsi, radial forearm, and lateral arm flaps) are used for this purpose.
The orbit is closed with temporal flaps, the eyelids, or a partial- or full-thickness skin graft. Muscle only, rather than fascia, should be used to improve the nutrition of the skin graft. The volume of the temporalis muscle used is smaller than with other muscles. It covers the orbit from the lateral orbital wall to the nose like a curtain. Recurrence in the orbit, skull base, and nasal cavity can then be evaluated via nasal endoscopy. This procedure also avoids the shortcoming of primary reconstruction hiding recurrence [13].
CT and MRI are useful modalities for evaluating the characteristics, anatomical site, and extent of suspected orbital involvement. CT and MRI can also be used during in follow-up to monitor recurrences. A local flap that covers the orbit will not hide recurrences [10].
The most common complication is a defect in the temporal region. With most local and free flaps, donor defects can occur, affecting the patient's aesthetic appearance. In our cases, the flaps were prepared from the posterior 1/3 or 1/4 of the temporalis muscle, which prevents a donor defect.
Another important consideration is the risk of injury to the frontal branch of the facial nerve on the temporalis muscle during elevation of the skin. This nerve is located between the two layers of temporoparietal fascia in the fat tissue. When the skin flap includes the fat tissue over the internal layer of the fascia, it is not at risk. While preparing the flap, injury may occur as a result of stretching the nerve, but this is a reversible condition. In this study, three patients had frontal facial paralysis.
Free flaps extend the nature of the operation and an additional team is needed. By contrast, the temporal flap is adjacent to the orbit, and requires only an incision in the scalp, which will be hidden by the scalp, and is easy to elevate.
Chemotherapy and radiotherapy should be combined in order to treat advanced disease for palliation. Osteoradionecrosis, osteomyelitis, and eye complications can be seen in follow-up.
Follow-up for recurrences in this study was performed in two ways: endoscopic examination of the nasal cavity and radiology. The temporalis muscle flap is not as thick as free flaps, and the recurrence can be diagnosed readily by endoscopic nasal examination. However, this is not always enough. Radiologic examination of the skull base and orbital cavity can be used for recurrences and follow-up as well. MRI and CT help to diagnose brain and skull base involvement respectively. Recently fluorodeoxyglucose positron emission tomography/CT scan has been used for recurrences and distant metastasis. In this study, three patients died with recurrences while two patients died of systemic metastases.
After orbital reconstruction, various ocular prostheses can be used as requested by the patient, including hydroxyapatite implants, polymethylmethacrylate prostheses, and bone-implanted dentures [14,15].
The temporalis muscle flap was preferred for reconstruction in this study. This flap has a good vascularization and it is close to the defect region. It is easy to perform and adequate in terms of length, width and volume. Additionally, it has better vascularization than dermal and skin grafts and results in a better cosmetic appearance. It has a short healing time compared to secondary wound healing. Also it has a short operation time and less visible scar in the donor site compared to the free flap technique. This is a thin flap, making it easy to follow-up for recurrences with nasal endoscopy. The temporalis muscle flap should be preferred for primary reconstruction of orbital exenteration defect.

Notes

No potential conflict of interest relevant to this article was reported.

References

1. Kennedy RE. Indications and surgical techniques for orbital exenteration. Ophthalmology. 1979; 5. 86(5):967–973. PMID: 397452.
crossref
2. Rose GE, Wright JE. Exenteration for benign orbital disease. Br J Ophthalmol. 1994; 1. 78(1):14–18. PMID: 8110691.
crossref
3. Hargrove RN, Wesley RE, Klippenstein KA, Fleming JC, Haik BG. Indications for orbital exenteration in mucormycosis. Ophthal Plast Reconstr Surg. 2006; Jul-Aug. 22(4):286–291.
crossref
4. Cook BE Jr, Bartley GB. Treatment options and future prospects for the management of eyelid malignancies: an evidence-based update. Ophthalmology. 2001; 11. 108(11):2088–2098. PMID: 11713084.
crossref
5. Rahman I, Cook AE, Leatherbarrow B. Orbital exenteration: a 13 year Manchester experience. Br J Ophthalmol. 2005; 10. 89(10):1335–1340. PMID: 16170127.
crossref
6. Nassab RS, Thomas SS, Murray D. Orbital exenteration for advanced periorbital skin cancers: 20 years experience. J Plast Reconstr Aesthet Surg. 2007; 60(10):1103–1109. PMID: 17434350.
crossref
7. Hussain A, Murthy P, Silver SM. Pedicled temporoparietal galeal myofascial flap for orbital and cheek lining following radical maxillectomy. Rhinology. 1996; 12. 34(4):227–231. PMID: 9050102.
8. Cuesta-Gil M, Concejo C, Acero J, Navarro-Vila C, Ochandiano S. Repair of large orbito-cutaneous defects by combining two classical flaps. J Craniomaxillofac Surg. 2004; 2. 32(1):21–27. PMID: 14729046.
crossref
9. Roche P, Timon C. Orbital exenteration in periorbital malignancies. Surgeon. 2012; 8. 10(4):189–193. PMID: 22818275.
crossref
10. Ben Simon GJ, Schwarcz RM, Douglas R, Fiaschetti D, McCann JD, Goldberg RA. Orbital exenteration: one size does not fit all. Am J Ophthalmol. 2005; 1. 139(1):11–17. PMID: 15652823.
11. Guerra AS, Barbosa R, Choupina M, Pinho C, Ribeiro M, Pontes L. Orbital exenteration for eyelid skin carcinoma. Eur J Plast Surg. 2011; 8. 34(4):239–243.
crossref
12. Serrano NA, Trenite GN, Yueh B, Farwell DG, Futran ND, Mendez E. Risk factors associated with repair of orbital and lateral skull defects. Arch Facial Plast Surg. 2012; Mar-Apr. 14(2):97–103. PMID: 22183060.
crossref
13. Howard DJ, Lund VJ, Wei WI. Craniofacial resection for tumors of the nasal cavity and paranasal sinuses: a 25-year experience. Head Neck. 2006; 10. 28(10):867–873. PMID: 16823871.
crossref
14. Gil Z, Abergel A, Leider-Trejo L, Khafif A, Margalit N, Amir A, et al. A comprehensive algorithm for anterior skull base reconstruction after oncological resections. Skull Base. 2007; 2. 17(1):25–37. PMID: 17603642.
crossref
15. Zins JE, Moreira-Gonzalez A, Papay FA. Use of calcium-based bone cements in the repair of large, full-thickness cranial defects: a caution. Plast Reconstr Surg. 2007; 10. 120(5):1332–1342. PMID: 17898609.
crossref
Fig. 1
A 65-year-old man with a malignant tumor invading the orbit. (A) Preoperative photography of the exophytic malignant tumor, which invades the eye and the orbit. (B) The axial magnetic resonance imaging scans were interpreted as solid, irregular enhancement invading the eye and orbit. (C) Intraoperative operative technique of the orbital exenteration of the eye. (D) Postoperative temporalis muscle flap closure with full-thickness skin graft.
ceo-8-52-g001
Fig. 2
The surgical technique. (A) The temporoparietal fascia is elevated with a skin flap. The zygomatic arch and lateral orbital wall of the outer surface are exposed. (B) An osteotomy is made in the zygomatic arch and the temporalis muscle flap is elevated from the junction of the perichondrium subperiosteally. (C) A tunnel is created by drilling in the lateral orbital wall, and the flap is laid down.
ceo-8-52-g002
Fig. 3
A 54-year-old woman with squamous cell carcinoma in the ethmoid sinus invading the left orbit. (A) Preoperative photography of the patient with proptosis in the left eye. (B) The axial computed tomography scans were interpreted as a solid mass in the etmoid air cells invading the nasal septum, left lamina papyracea and left optic nerve. (C) Intraoperative operative technique of the tunnel created to ensure the passage of the temporalis muscle flap to the orbit. (D) Postoperative temporalis muscle flap closure with the eyelid skin.
ceo-8-52-g003
Table 1.
Histological diagnosis of the tumors
Histological diagnosis No. of cases
Skin 6
 Basal cell carcinoma 2
 Squamous cell carcinoma 4
Nasal cavity and paranasal sinus 7
 Adenocarcinoma 1
 Olfactory neuroblastoma 1
 Adenoid cystic carcinoma 1
 Mucoepidermoid carcinoma 1
 Squamous cell carcinoma 3
Table 2.
Compartments affected by the tumor in the orbit
Compartment No. of cases
Anterior compartment of the orbit 10
 Orbital apex 8
 Superior wall of the orbit 7
Inferior wall of the orbit 5
 Muscle invasion 5
 Periorbital invasion 13
Table 3.
Complications of the temporal muscle flap
Complication No. of cases
Frontal paralysis 3
Temporal deformity 0
Orbital fistula 2
TOOLS
Similar articles