Journal of Cranio-Maxillofacial Surgery (2001) 29, 337–343
r 2001 European Association for Cranio-Maxillofacial Surgery
doi:10.1054/jcms.2001.0253, available online at http://www.idealibrary.com on
Repair of composite zygomatico-maxillary defects with free bone grafts and
free vascularized tissue transfer
Dennis Rohner,1,2 Bien-Keem Tan,1 Colin Song,1 Vincent Yeow,1 Beat Hammer2
1
Department of Plastic Surgery (Head: Dr. Kok Chai Tan), Singapore General Hospital, Singapore;
Department of Reconstructive Surgery (Head: Prof. Dr. Dr. Joachim Prein), University Hospital Basel,
Basel, Switzerland
2
SUMMARY. Introduction: Three-dimensional repair of the zygomatico-maxillary defect calls for an elaborate
technique to achieve facial symmetry and correct globe position. We present a technique, which combines the use of
a free vascularized soft tissue flap and free bone grafts for repair of composite zygomatico-maxillary defects.
Patients: Three patients that underwent radical resection of the maxilla and the zygoma have undergone facial
reconstruction using this technique. The mean follow up was 9 months. Methods: The key points of this technique
are: (1) precise reconstruction of the zygomatico-maxillary complex including the orbit; (2) creation of a skeletal
framework for canthopexy and suspension of the free flap; (3) repair of through-and-through soft tissue defects with
a folded musculocutaneous free flap; and (4) simultaneous harvesting and reconstruction using two surgical teams to
reduce the duration of surgery. Results: Reconstruction of the zygomatico-maxillary complex could be successfully
accomplished in a single surgical procedure. Conclusion: This paper presents a method of repairing zygomaticomaxillary defects with free bone grafts and vascularized soft tissue. However, this concept has yet to be reviewed in
the long term. r 2001 European Association for Cranio-Maxillofacial Surgery
maxilla using split rib grafts (Obwegeser 1973; Brown
et al., 1978). But only Brown et al. (1978) used bone
grafts in combination with a free vascularized
omentum flap: Two recent reports highlighted the
advantages of using free calvarial bone grafts in
combination with free flaps: Cordeiro et al. (1998)
described primary repair of maxillectomy defects
using free bone grafts in combination with a free
rectus abdominis myocutaneous flap. Posnick et al.
(1992) presented a case of free vascularized radial
forearm flap and free calvarial bone grafts for the
reconstruction of the zygomatico-maxillary complex.
The purpose of our report is to describe our
technique of reconstructing the zygomatico-maxillary
complex using free bone grafts in combination with a
myocutaneous free flap. The key points of our
technique are: (1) precise reconstruction of the malar
prominence, orbital walls and orbital floor to
maintain facial symmetry and globe position; (2)
creation of a skeletal framework for canthopexy and
suspension of the free flap; and (3) adequate soft
tissue replacement for bulk, skin cover, and oro-nasal
lining.
INTRODUCTION
Various classifications exist for maxillectomy defects
(Brown et al., 2000; Cordeiro and Santamaria, 2000;
Spiro et al., 1997). These defects range from minor,
such as those following limited resection of the
alveolus, to major defects following total maxillectomy. Total maxillectomy defects may be divided into
those sparing the globe and those with orbital
exenteration. We have classified our patients with
maxillary defects according to the horizontal and
vertical extents of resection (Table 1) as described by
Brown et al. (2000).
Zygomatico-maxillary defects are complex following resection of tumours of the maxilla and zygoma.
They may be associated with loss of bone, skin, oronasal lining, and soft tissue depending on the tumour.
Reconstruction must address all aspects including the
skeleton and soft tissue (skin, bone and mucosa). The
aims of skeletal reconstruction are to restore correct
facial dimensions (facial width and malar projection)
and to provide support for the globe. Soft tissue
reconstruction involves replacement of skin and oronasal lining. Soft tissue bulk must be adequate to
obliterate dead space and to anticipate post-irradiation contracture.
Most reports describe one-stage reconstruction
using microvascular composite tissue transfer (Brown
1996; Browne and Burke, 1999; Cordeiro et al., 1998;
Foster et al., 1997; Granick et al., 1990; Jortay et al.,
1994; Kazaoka et al., 1999; Kyutoku et al., 1999; Lee
et al., 1999; Nakayama et al., 1994; Schusterman
et al., 1993; Yamada et al., 1996; Yamamoto et al.,
1987). Two reports describe reconstruction of the
PATIENTS AND METHODS
Between March and August of 2000, three patients
underwent radical resection of the maxilla and
zygoma. The primary diagnoses were Ewing’s sarcoma, adenoidcystic carcinoma, and poorly differentiated squamous cell carcinoma (Table 2). Resection
of the orbital floor was carried out preserving the
orbital contents. Due to tumour involvement, the
337
338 Journal of Cranio-Maxillofacial Surgery
Table 1 – Maxillectomy classification from Brown et al., 2000
Vertical
Horizontal
1 Maxillectomy without
oro-antral fistula
2 Low maxillectomy
3 High maxillectomy
a unilateral alveolus of maxilla and
hard palate less than or equal to
the midline
b resection crossing the midline
c entire alveolus of maxilla and
hard palate
4 Radical maxillectomy
resections included skin, oral and nasal linings. The
head and neck surgeon or maxillofacial surgeon
performed tumour extirpation. All resection margins
were subjected to frozen section analysis before
proceeding with repair. Reconstruction was undertaken by two teams working simultaneously – the
plastic surgeons who harvested the free flap and the
maxillofacial team who assembled the orbitozygomatic complex.
Technical aspects
Skeletal reconstruction was carried out in patients 2
and 3 with free split calvarial bone grafts harvested
through limited coronal approaches using the technique described by Jackson et al. (1986) and Frodel
et al. (1993). Six pieces of bone, each measuring
1 4 0.3 cm, were sufficient to reconstruct the
medial and lateral orbital walls, lateral orbital rim,
orbital floor, infraorbital rim and zygomatic arch.
For patient 1 who was in the paediatric age group,
the 7th and 8th ribs were harvested from the right
chest, split and cut into six pieces to create the
zygomatic skeletal framework (Fig. 1).
The bone grafts were fixed to the base of the
zygomatic arch, supraorbital rim, residual medial and
lateral orbital walls and the cranial base, lateral to the
pterygoid fossa by means of titanium miniplates
(Synthess, Mathys Medical, Bettlach, Switzerland).
Miniplates (1.5 mm) were used for orbital reconstruction, 2.0 mm plates were employed at the base of the
zygomatic arch and for the zygomatic body for
greater rigidity. The medial orbital wall bone graft
was fixed to the remaining part of the wall. In cases
where the medial wall had been completely resected,
it was secured to nasion and glabella. The posteromedial wall and orbital floor were reconstructed with
a single bone graft attached to the base of the middle
cranial fossa. Upon completion, the position of the
globe was checked by comparison with the opposite
side. Medial and lateral canthopexies were performed
by attaching the respective canthal ligaments to the
newly created framework with non-resorbable sutures.
A free musculocutaneous flap was used to reconstruct the through-and-through cheek defect. To
create outer and inner linings, the flap was folded
on itself and its central portion de-epithelialized. The
intraoral portion was first inset to establish a seal.
The muscle and fascia of the flap were then sutured to
the reconstructed orbital rim for suspension. Likewise, the skin and subcutaneous tissue at the upper
border of the flap were anchored to the bone grafts to
prevent traction on the lower eyelid.
Case report
This 74-year-old patient (patient 3) had a poorly
differentiated squamous cell carcinoma of the left
maxilla (Fig. 2). The resection was a type 3a
maxillectomy including the body of the zygoma,
cheek skin and oral mucosa. The globe was spared.
Because of neural invasion, the facial nerve and its
branches were sacrificed. Reconstruction of the
zygomatico-maxillary complex was acomplished with
free calvarial bone grafts, soft tissue reconstruction
with a folded anterolateral thigh flap, suspended from
the bone graft scaffold (Fig. 3). Healing was
uneventful and the patient commenced radiotherapy
6 weeks postoperatively. Postoperative CT scans
revealed slight overcorrection of the zygoma, which
was necessary for soft tissue support (Fig. 4). Clinical
assessment showed good facial symmetry and malar
projection; there was no ectropion (Fig. 5).
RESULTS
The flap survival was complete in all three cases.
Reconstruction of the bone framework was successful
and healed uneventful. Two patients (patients 1 and
3) underwent radiotherapy without complications.
The donor sites were closed in all three patients
primarily. The function of the lower limb from
patients 2 and 3, and of the upper limb and shoulder
from patient 1 did not show any impairment in
comparison to the contralateral side at 3 months. The
function of the involved eye was not impaired and
none of the patients experienced double vision. The
mean follow up was 9 months (7–11 months). Patient
2 needed some debulking of the soft tissue flap in a
secondary surgical procedure 4 months after the
primary reconstruction.
Table 2 – Patient records
Patient
Age (Years)
Diagnosis
Location
Resection
Reconstruction
1
2
3
5
49
74
Ewing’s sarcoma
Adenoidcystic carcinoma
Poorly differentiated
squamous cell
carcinoma
Left maxilla
Right maxilla
Left maxilla
3b+zygoma
3a+zygoma
3a+zygoma
RG+LD
SCG+ALT
SCG+ALT
RG – free rib graft; SCG=split calvarial graft; LD=latissimus dorsi free flap; ALT – anterolateral thigh free flap.
Repair of composite zygomatico-maxillary defects 339
Fig. 1 – Cadaveric demonstration. (A) Reconstruction starts at base of the zygomatic arch (1). The natural curvature of the graft reproduces
the shape of the zygomatic arch. For adequate globe support, the posterior orbital floor is reconstructed with a graft secured to the cranial
base (2). (B) The bone graft attached to the remnant of the medial orbital wall or to the orbital roof (3) to reconstruct the orbital wall. The
frontozygomatic buttress reconstructed with a bone graft joined at right angles to the zygomatic arch (4). This graft creates the malar
prominence. Overcorrection is desirable to overcome the effects of soft tissue shrinkage. (C) Fixation of the infraorbital bone graft (5)
completes the zygomaticomaxillary complex. Additional bone grafts may be placed to create the lateral orbital wall (6) and to augment the
floor (7). (D) Oblique view of the complete zygomatico-maxillary complex.
DISCUSSION
Extended ablative surgery of the midface results in
disfigurement and functional disability. Even with the
latest techniques, satisfactory reconstruction of the
total zygomatico-maxillary complex is a formidable
challenge, particularly in cases where there is
associated soft tissue loss. To date, there are no
reports focusing exclusively on the repair of throughand-through zygomatico-maxillary defects (i.e. oronasal lining, bone and skin).
Techniques for maxillectomy reconstruction may
be broadly divided into three categories: (1) free
vascularized soft tissue flap without skeletal reconstruction (Browne and Burke, 1999; Yamamoto et al.,
1987); (2) free bone grafts in conjunction with free
vascularized tissue (Cordeiro et al., 1998; Pollice and
Frodel 1998); and (3) osteocutaneous/osteomyocutaneous free flaps (Brown, 1996; Foster et al., 1997;
Granick et al., 1990; Holle et al., 1996; Igawa et al.,
1998; Kazaoka et al., 1999; Kyutoku et al., 1999; Lee
et al., 1999; Nakayama et al., 1994; Schusterman
et al., 1993; Yamada et al., 1996). Bone grafts in
conjunction with free vascularized tissue were employed in our three patients who all had composite
zygomatico-maxillary defects. The advantages of this
approach are:
Firstly, a precise reconstruction of the orbitozygomatic complex can be accomplished with bone grafts.
Based on Gruss’ principles (Gruss and Mackinnon
1986), malar projection and facial width are restored
by recreating the zygomatico-maxillary and nasomaxillary buttresses using rigid fixation techniques
(Manson et al., 1980). Soft tissue cover is achieved
340 Journal of Cranio-Maxillofacial Surgery
Fig. 2 – Patient no 3. (A & B) Coronal and axial CT scans depicting maxillary squamous cell carcinoma occupying the entire antrum and
invading the orbital floor and cheek. (C) Preoperative view.
Fig. 3 – Intraoperative views (patient no. 3). (A) Completed zygomatico-maxillary buttress. (B) Posterior orbital floor reconstruction; bone
graft secured to cranial base with a miniplate (arrow). (C) Anterolateral thigh flap based on the descending lateral circumflex femoral vessels.
Fig. 4 – Postoperative CT scans (patient no. 3). (A) Axial view demonstrating skeletal asymmetry. (B) Maxillary region completely filled with
muscle to vascularize calvarial grafts and to obliterate dead space. (C) Anterior view; overcorrection of orbital floor to prevent
enophthalmos.
Repair of composite zygomatico-maxillary defects 341
Fig. 5 – Two weeks postoperatively (A) Symmetrical facial contour despite facial nerve resection. Suspension of the free flap from the orbital
rim prevented ectropion and sagging of the cheek. (B) Globe position maintained; no enophthalmos.
with a free musculocutaneous flap draped over the
bony scaffold. Cordeiro et al. (1998) reported a series
of maxillectomy repairs employing bone grafts and
free vascularized soft tissue. The authors favoured
this technique because bone and soft tissue could be
independently inset without compromising the microvascular aspects of the reconstruction. In contrast,
one limitation of composite free flaps (e.g. fibula
osteocutaneous flap, scapula osteocutaneous flap,
rectus abdominis myocutaneous flap with costal
cartilage) is the inability to reconstruct the orbitozygomatic skeleton precisely because of soft tissue
attachments to bone maintained for osseous vascularity. Free vascularized soft tissue alone is unlikely
to be adequate due to the absence of skeletal support.
Yamamoto et al. (1987) described the use of a single
osteomyocutaneous free flap to reconstruct the
zygomatico-maxillary, naso-maxillary and pterygomaxillary buttresses in a maxillectomy defect. However, the procedure was simplified by the presence of
intact skin, allowing the authors to focus entirely on
reconstruction of skeletal structure and oral lining.
Even so, an additional scapula bone graft was
necessary for orbital floor reconstruction. Similarly,
Nakayama et al. (1994) used a fibula osteocutaneous
flap for reconstruction of the maxilla in a case
without skin defect. The bone was osteotomised into
three segments to reconstruct the infraorbital rim,
orbital floor and zygomatic arch.
Secondly, the technique allows precise placement
of calvarial bone grafts for globe support. To prevent
enophthalmos or other dystopia, attention is focused
on key areas such as the posteromedial orbital wall
and lateral orbital wall (Hammer, 1995). Fine
adjustment to the position of the globe can be
effected by layering grafts. Foster et al. (1997)
highlighted the difficulty of fabricating the entire
orbitozygomatic complex with a single composite free
flap for midface reconstruction. The authors proposed the fibula flap for complex midfacial defects,
but qualified this by stating that the orbital floor
required additional support with bone grafts or
titanium mesh. Granick et al. (1990) preferred the
osteocutaneous scapular flap, but also conceded that
support for the posteromedial wall of the orbit was
problematic without separate pieces of bone graft.
Thirdly, the assembled skeletal framework provides anchoring points for soft tissue support and
suspension. To prevent telecanthus and lower lid
laxity, medial and lateral canthopexies are performed
by reattaching the respective canthal ligaments to
predetermined points on the orbital rim (Hammer,
1995). Additionally, the free flap is suspended from
the orbital rim to prevent sagging and traction on the
lower eyelid. Granick et al. (1990) reported a case of
postoperative ectropion due to its unsupported
weight when using an osteocutaneous scapular flap.
Controversies exist concerning the use of free bone
grafts for facial reconstruction following tumour
ablation. Since most patients require postoperative
radiotherapy, there is concern regarding the risk of
infection, extensive resorption and osteoradionecrosis
(Coleman, 1994; Kyutoku et al., 1999; Lee et al.,
1999). Nevertheless, several animal studies showed
that rational radiotherapy after insertion of a bone
graft did not endanger the graft survival (DeSantis
et al., 1990; Roy-Camille et al., 1981; Schwartz et al.,
1986). Cordeiro et al., (1998) reported good tolerance
of bone grafts to radiation when the grafts were used
in conjunction with free flaps for reconstruction of
the maxilla. Ten of 14 patients received postoperative
radiotherapy. Over a mean follow-up of 21 months
all primary bone grafts survived and the authors did
not detect any bone resorption or infection. We
342 Journal of Cranio-Maxillofacial Surgery
believe that the key to bone graft preservation is bone
revascularization. When placing the flap, care is
taken to ensure that the entire bony framework is
enveloped by vascularized muscle, since direct muscle-bone contact promotes vascularization of the free
bone grafts. This phenomenon was demonstrated by
Fisher and Wood (1987) in a pig model when free
bone grafts embedded in a muscle flap acquired
medullary circulation within 4 weeks. These results
could explain why rabbit bone grafts irradiated 4
weeks after surgery were less affected by irradiation
than those irradiated during the first 4 weeks, because
the grafts achieved sufficient new vascularity within 4
weeks (Morales et al., 1987). In our hospitals,
radiotherapy is usually administered 6 weeks postoperatively, a time interval which is probably
sufficient for osseous revascularization.
The second controversial issue relates to bone graft
resorption with time. In general, the rate of bone
resorption depends on bone vascularity and quality.
Several authors describe a high resorption rate of free
bone grafts when compared with vascularized grafts
(Antonyshyn et al., 1987; Fukuta et al., 1992; Gosain
et al., 1999). Fukuta et al., (1992) observed that
pedicled bone flaps in pigs retained their original
volumes, whereas free skull grafts lost approximately
50% of the initial volume after 3 months. Gosain
et al., (1999) observed a 15% loss in thickness of nonvascularized grafts over one year, compared with
vascularized grafts which maintained their initial
thickness over the same time period. With regard to
bone quality, Ozaki and Buchman (1998) noted that
cortical grafts maintained their volumes significantly
better than cancellous grafts. Furthermore, Motoki
and Mulliken (1990) demonstrated that membranous
bone (e.g. calvarial bone) underwent less resorption
and revascularized at a faster rate when compared
with endochondral bone (e.g. iliac crest). In our
technique, we favour calvarial bone grafts because of
their large cortical component, which confers mechanical strength and resistance to resorption. To
overcome the problem of resorption due to nonvascularity, the bone grafts are maintained in contact
with the flap, for reasons alluded to in the previous
section.
Finally, some technical refinements are worth
noting:
K To achieve an aesthetic outcome, overcorrection
of the contour of the zygoma is recommended.
Overcorrection helps to counterbalance the
effects of soft tissue shrinkage.
K The infraorbital rim is positioned 3–4 mm higher
than the opposite side for lower eyelid and flap
support.
K Overcorrection of the orbital floor and
posteromedial wall with bone grafts is essential
to prevent enophthalmos.
Apart from the question of bony repair of the
defect there is still the discussion about the choice of
the soft tissue flap. Whilst there may be different soft
tissue flaps that can be chosen, depending on the
location and size of the defect, we have chosen the
anterolateral thigh flap because it is extremely
versatile in design and composition with multiple
advantages like adequate tissue volume, minimal
donor site morbidity, potential for reinnervation,
large and long pedicle and the feasibility of the two
team approach. Two minor disadvantages of this flap
are the high incidence of hairy skin in that area in
male patients and donor site scars associated with the
use of skin grafts in large defects (Demirkan et al.,
2000). The major problem may be the variation in the
origin and course of the supplying perforators, which
is present in 12–18% of patients (Demirkan et al.,
2000; Kimata et al., 1998). However, the anterolateral
thigh flap is a good choice for reconstruction of any
type of defects after tumour resection in the head and
neck area.
CONCLUSION
We describe the reconstruction of through-andthrough zygomaticomaxillary defects using free bone
grafts and a free vascularized soft tissue flap. This
technique was successful in three patients with a
mean follow up period of 9 months. The advantage of
this technique was on the one hand the precise
reconstruction of the orbitozygomatic complex with
free bone grafts, which could be accomplished
independently from the free vascularized soft tissue
flap. One the other hand the reconstruction of the
oral lining and the repair of the skin defect could be
performed with a folded soft tissue flap draped over
the bony orbitozygomatic scaffold. The simultaneous
two team approach is another advantage for reducing
the time of surgery. We believe that the use of free
bone grafts in combination with a free vascularized
soft tissue flap for the repair of zygomaticomaxillary
defects is superior to the use of composite free
vascularized osteomyocutaneous flaps.
Acknowledgements
The authors gratefully acknowledge Mathys Singapore for providing the miniplates for skull demonstration. We wish to thank Dr
Wee Keng Poh, Director of the Department of Forensic Medicine,
Institute of Science and Forensic Medicine, Singapore, for the
cadaveric specimens; and Mr Gao Hong and Mr Robert Ng of the
Department of Experimental Surgery, Singapore General Hospital,
for technical support.
References
Antonyshyn O, Colcleugh RG, Anderson C: Growth potential in
suture bone inlay graft: a comparison of vascularized and free
calvarial bone grafts. Plast Reconstr Surg 79: 1–9, 1987
Brown JS: Deep circumflex iliac artery free flap with internal
oblique muscle as a new method of immediate reconstruction
of maxillectomy defect. Head Neck 18: 412–421, 1996
Brown JS, Rogers SN, McNally DN, Boyle M: A modified
classification for the maxillectomy defect. Head Neck 22:
17–26, 2000
Brown RG, Nahai F, Silverton JS: The omentum in facial
reconstruction. Br J Plast Surg 31: 58–62, 1978
Repair of composite zygomatico-maxillary defects 343
Browne JD, Burke AJ: Benefits of routine maxillectomy and orbital
reconstruction with the rectus abdominis free flap. Otolaryngol
Head Neck Surg 121: 203–209, 1999
Coleman JJ 3rd: Osseous reconstruction of the midface and orbits.
Clin Plast Surg 21: 113–124, 1994
Cordeiro PG, Santamaria E: A classification system and algorythm
for reconstruction of maxillectomy and midfacial defects. Plast
Reconstr Surg 105: 2331–2346, 2000
Cordeiro PG, Santamaria E, Kraus DH, Strong EW, Shah JP:
Reconstruction of total maxillectomy defects with preservation
of the orbital contents. Plast Reconstr Surg 102: 1874–1884,
1998
Demirkan F, Chen HC, Wei FC, Chen HH, Jung SG, Hau SP,
Liao CT: The versatile anterolateral thigh flap: a
musculocutaneous flap in disguise in head and neck
reconstruction. Br J Plast Surg 53: 30–36, 2000
De Santis G, Williams JF, Dvir E, O’Brien BM, Hurley JV,
Goldberg I: Effect of postoperative radiation on the
incorporation of tibial bone grafts in the rabbit. J Bone Joint
Surg Br 72: 309–311, 1990
Fisher J, Wood MB: Experimental comparison of bone
revascularization by musculocutaneous and cutaneous flaps.
Plast Reconstr Surg 79: 81–90, 1987
Foster RD, Anthony JP, Singer MI, Kaplan MJ, Pogrel MA,
Mathes SJ: Reconstruction of complex midfacial defects. Plast
Reconstr Surg 99: 1555–1565, 1997
Frodel JL, Marentette LJ, Quatela VC, Weinstein GS: Calvarial
bone graft harvest: techniques, considerations, and morbidity.
Arch Otolaryngol Head Neck Surg 119: 17–23, 1993
Fukuta K, Har-Dhai Y, Collares MV, Herschman BR, Persiani RJ,
Jackson IT: The viability of revascularized calvarial bone graft
in a pig model. Ann Plast Surg 29: 136–142, 1992
Gosain AK, Song L, Santoro TD, Amarante MTJ, Simmonds DJ:
Long-term remodeling of vascularized and nonvascularized
onlay bone grafts: a macroscopic and microscopic analysis.
Plast Reconstr Surg 103: 1443–1450, 1999
Granick MS, Ramasastry SS, Newton ED, Solomon MP, Hanna
DC, Kaltman S: Reconstruction of complex maxillectomy
defects with the scapular-free flap. Head Neck 12: 377–385,
1990
Gruss JS, Mackinnon SE: Complex maxillary fractures: Role of
buttress reconstruction and immediate bone grafts. Plast
Reconstr Surg 78: 9–22, 1986
Hammer B: Operative management of orbital fractures, In:
Hammer B (ed.). Orbital Fractures – Diagnosis, Operative
Treatment, Secondary Corrections. Hogrefe & Huber
Publishers, Seattle, Toronto, Bern, Göttingen 1995, 43–58
Holle J, Vinzenz K, Wuringer E, Kulenkampff KJ, Saidi M: The
prefabricated combined scapula flap for bony and soft-tissue
reconstruction in maxillofacial defects–a new method. Plast
Reconstr Surg 98: 542–52, 1996
Igawa HH, Minakawa H, Sugihara T: Functional alveolar ridge
reconstruction with prefabricated iliac crest free flap and
osseointegrated implants after hemimaxillectomy: case report.
Plast Reconstr Surg 102: 2420–2424, 1998
Jackson IT, Helden G, Marx R: Skull bone grafts in maxillofacial
and craniofacial surgery. Oral Maxillofac Surg 44: 949–955,
1986
Jortay A, Coessens B, Greant P, Bisschop P: Use of osteomuscular
free flaps after extended maxillectomy and craniofacial
resection. About two cases. Acta Chir Belg 94: 236–239, 1994
Kazaoka Y, Shinohara A, Yokou K, Hasegawa T: Functional
reconstruction after a total maxillectomy using a fibula
osteocutaneous flap with osseointegrated implants. Plast
Reconstr Surg 103: 1244–1246, 1999
Kimata Y, Uchiyama K, Ebihara S, Nakatsuka T, Harii K:
Anatomic variations and technical problems of the
anterolateral thigh flap: a report of 74 cases. Plast Reconstr
Surg 102: 1517–1523, 1998
Kyutoku S, Tsuii H, Inoue T, Kawakami K, Han F, Ogawa Y:
Experience with the rectus abdominis myocutaneous flap with
vascularized hard tissue for immediate orbitofacial
reconstruction. Plast Reconstr Surg 103: 395–402, 1999
Lee HB, Hong JP, Kim KT, Chung YK, Tark KC, Bong JP:
Orbital floor and infraorbital rim reconstruction after total
maxillectomy using a vascularized calvarial bone flap. Plast
Reconstr Surg 104: 646–653, 1999
Manson PN, Hoopes JE, SU CT: Structural pillars of the facial
skeleton: An approach to the management of Le Fort
fractures. Plast Reconstr Surg 66: 54–62, 1980
Morales MJ, Marx RE, Gottlieb CF: Effects of pre- and
postoperative irradiation on the healing of bone grafts in the
rabbit. J Oral Maxillofac Surg 45: 34–41, 1987
Motoki DS, Mulliken JB: The healing of bone and cartilage. Clin
Plast Surg 17: 527–544, 1990
Nakayama B, Matsuura H, Hasegawa Y, Ishihara O, Hasegawa H,
Torii S: New reconstruction for total maxillectomy defect with
a fibula osteocutaneous free flap. Br J Plast Surg 47: 247–249,
1994
Obwegeser HL: Late reconstruction of large maxillary defects after
tumour resection. J Maxillofac Surg 1: 19–23, 1973
Ozaki W, Buchman SR: Volume maintenance of onlay bone grafts
in the craniofacial skeleton: Micro-architecture versus
embryologic origin. Plast Reconstr Surg 102: 291–299,
1998
Pollice PA, Frodel IL Jr: Secondary reconstruction of upper
midface and orbit after total maxillectomy. Arch Otolaryngol
Head Neck Surg 124: 802–808, 1998
Posnick JC, Polley JW, Zuker RM, Chan HSL: Chemotherapy and
surgical resection combined with immediate reconstruction in
a 1-year-old child with rhabdomyosarcoma of the maxilla.
Plast Reconstr Surg 89: 320–325, 1992
Roy-Camille R, Laugier A, Ruyssen S, Chenal C, Bisserie M, Pene
F, Saillant G: Evolution des greffes osseuses corticospongieuses et radiotherapie. Rev Chir Orthop Reparatrice
Appar Mot 67: 599–608, 1981
Schusterman MA, Reece GP, Miller MJ: Osseous free flaps for
orbit and midface reconstruction. Am J Surg 166: 341–345,
1993
Schwartz HC, Leake DL, Kagan AR, Snow H, Pizzoferrato A:
Postoperative irradiation of fresh autogenic cancellous bone
grafts. Plast Reconstr Surg 77: 122–126, 1986
Spiro RH, Strong EW, Shah JP: Maxillectomy and its
classification. Head Neck 19: 309–314, 1997
Yamada A, Harii K, Ueda K, Nakatsuka T, Asato H, Kajikawa A:
Secondary contour reconstruction of maxillectomy defects
with a bone graft vascularized by flowthrough from radial
vascular system. Microsurgery 17: 141–145, 1996
Yamamoto K, Takagi N, Miyashita Y, Hirabayashi M, Goto A:
Facial reconstruction with latissimus dorsi myocutaneous
island flap following total maxillectomy. J CranioMaxillofac
Surg 15: 288–90, 1987
Dennis Rohner, MD, DMD
Department of Reconstructive Surgery
Clinic of Maxillofacial Surgery
University Hospital Basel
Spitalstrasse 21 CH-4031 Basel,
Switzerland
Tel: +41 61 265 7344
Fax: +41 61 265 7458
E-mail: dennisrohner@hotmail.com
Paper received 8 November 2000
Accepted 25 September 2001