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Otolaryngology–Head and Neck Surgery (2007) 136, 920-927

ORIGINAL RESEARCH

Surgical outcomes and safety of transnasal


endoscopic resection for anterior skull tumors
Sandeep P. Dave, MD, Anthony Bared, MD, and Roy R. Casiano, MD,
Miami, FL
associated with significant morbidity and perioperative mor-
OBJECTIVE: To report the surgical outcomes and safety of tality.1-5
transnasal endoscopic resection (TER) for anterior skull base In the late 1990s, endoscopic-assisted CFR, in which the
(ASB) tumors. ASB is approached via bifrontal craniotomy from above and
STUDY DESIGN AND SETTING: A retrospective chart re-
endoscopically from below, was first described.1,6-8 From
view to identify patients undergoing TER for ASB tumors at a
1999 to 2001, Stammberger et al,9 Walch et al,10 and Unger
tertiary care medical center between September 1997 and June
2006. et al11 reported a series of patients with olfactory neuroblas-
RESULTS: Nineteen patients underwent TER for ASB tumors toma who were treated with a combination of transnasal
without open craniotomy. There were 17 malignant and two be- endoscopic resection (TER) and adjuvant stereotactic radio-
nign lesions. Olfactory neuroblastoma was the most common pa- surgery. All tumors were removed piecemeal; in the major-
thology, occurring in 53 percent of patients. One patient recurred ity of cases, the ASB bone and the overlying dura were
locally, resulting in an overall local control rate of 94.7 percent for preserved. Since then, several authors12-14 have reported
all neoplasms and 94.1 percent for malignant disease. It should be case reports describing TER for various ASB tumors.
noted that the tumor control rate may be premature given the small In 2001, Casiano et al1 reported the first en bloc TER for
sample size and limited follow-up. Overall, there were 16 compli- an ASB tumor that included both the skull base bone and
cations, but only two of these, an orbital hematoma and a frontal overlying dura, without the need for open craniotomy.
lobe abscess, were considered major complications directly attrib-
Three of the patients underwent a formal endoscopic resec-
utable to surgery.
tion, which included the crista galli, perpendicular plate,
CONCLUSIONS: TER for ASB tumors appears to be safe in
properly selected patients. In light of the small sample size and
cribriform plate, olfactory bulb, and overlying dura. The
limited follow-up, the major complication rate directly attributable operative technique has been previously described in detail
to surgery was 11 percent, and the overall local control rate was 95 and is only briefly reviewed here.1,15 After the inferior
percent. A larger multi-institutional series with longer follow-up is aspect of the nasal septum is removed to the level of unin-
warranted. volved margins, extended frontal and sphenoid sinusoto-
© 2007 American Academy of Otolaryngology–Head and Neck mies are performed. Next, the fovea ethmoidalis and sphe-
Surgery Foundation. All rights reserved. noid planum (anterior to the optic chiasm) are thinned and
removed to expose the overlying dura circumferentially,

T raditional craniofacial resection (CFR), which com-


bines a bifrontal craniotomy and a transfacial approach,
has been the gold standard for treatment of anterior skull
which is subsequently incised. Dural margin specimens are
sent for frozen-section analysis prior to en bloc removal of
the inferior crista galli, perpendicular plate, cribriform plate,
base (ASB) neoplasms. However, this approach has been olfactory bulb, and overlying dura.

From the Department of Otolaryngology–Head and Neck Surgery, yngology–Head and Neck Surgery, Toronto, Canada, September 17-20,
Jackson Memorial Medical Center and Sylvester Comprehensive Can- 2006.
cer Center, Leonard M. Miller School of Medicine, University of Reprint requests: Sandeep P. Dave, MD, University of Miami Hospital
Miami. and Clinics, 1475 NW 12th Avenue, Suite 4025 (D-1), Miami, FL 33136.
Dr. Casiano is a consultant for Gyrus ENT and Medtronic Xomed. E-mail address: sdave@med.miami.edu.
Presented at the Annual Meeting of the American Academy of Otolar-

0194-5998/$32.00 © 2007 American Academy of Otolaryngology–Head and Neck Surgery Foundation. All rights reserved.
doi:10.1016/j.otohns.2007.01.012
Dave et al Surgical outcomes and safety of transnasal . . . 921

Recently, Batra et al2 presented a comparison between not used for any of the cases, and neurosurgical support was
CFR (n ⫽ 16) and TER (n ⫽ 9) for ASB tumors. Six available at all times.
patients in the TER group underwent a purely endoscopic The extent of ASB resection was categorized into three
resection, while three patients required an endoscopic-as- groups: bilateral, unilateral, and partial (Fig 1). Bilateral or
sisted CFR to address obvious intracranial extension. Al- complete resection involved removal of the entire ASB,
though the cribriform plate was removed as the superior including the crista galli, perpendicular plate, cribriform
margin in the six cases of purely endoscopic resection, it is plate, olfactory bulb, and overlying dura circumferentially.
unclear whether the resection was performed en bloc and When these structures were removed as a single specimen,
whether the overlying dura was removed. Given the small it was considered an en bloc resection. Unilateral resection
sample size, they observed no statistically significant dif- involved removal of the cribriform plate and olfactory bulb
ferences between groups. However, there were several in- unilaterally. When these structures were removed as a single
teresting trends favoring the TER group for operative time, specimen with the adjacent dura and a portion of the crista
stay in the intensive care unit (ICU), major complications, galli and perpendicular plate, it was considered an en bloc
and mortality. They concluded that TER may offer less resection. When these structures were removed piecemeal
functional morbidity with equal efficacy compared with or when the crista galli and/or perpendicular plate were
CFR and that TER was a rational option in select patients. burred down from the side of the resection, it was consid-
In the present series, we report 19 cases of TER for ASB ered a non– en bloc resection. All other limited ASB resec-
tumors. To date, this represents the largest series in the tions that involved only a segment of the fovea ethmoidalis
literature of formal transnasal endoscopic resection of ASB and overlying dura were considered partial resections, and
tumors without the need for open craniotomy. We have therefore non– en bloc resections. Kuhn et al’s13 resection of
included four of the five patients from the senior author’s an ASB fibrosarcoma would be considered a partial resec-
previous series.1 Of the four patients included, review of the tion. For all bilateral and unilateral resections, the bony
histopathology from one of the patients revealed that the fovea ethmoidalis and sphenoid planum were removed in a
primary neoplasm was most likely a sinonasal undifferen- piecemeal fashion to gain exposure to the overlying dura.
tiated carcinoma (SNUC), not an olfactory neuroblastoma. The endoscopic view of a representative bilateral ASB de-
The one patient who was excluded from the present series fect is shown in Figure 2A.
was a case of recurrent olfactory neuroblastoma, which The operative technique for transnasal endoscopic ASB
required a revision endoscopic resection that did not involve resection and reconstruction has been previously described
the anterior skull base. in detail.1,15 All reconstruction materials were soaked in
polymyxin “bug juice” antibiotic solution. Early in the
study period, we used lyophilized dura and mucosal grafts
to reconstruct the ASB defect. Currently, we use a single
MATERIALS AND METHODS sheet of acellular dermal allograft/Alloderm (LifeCell Cor-
poration, Branchburg, NJ), a layer of Gelfoam (Pharmacia,
After the study protocol was approved by the institutional Kalamazoo, MI), and Merocel (Medtronic-Xomed, Jack-
review board, a retrospective chart review was performed to sonville, FL) tampons. The Merocel tampons were removed
identify patients undergoing TER for ASB tumors between within 5 days. The intraoperative view of a representative
September 1997 and June 2006 at the University of Miami/ Alloderm reconstruction is shown in Figure 2B. Prolonged
Jackson Memorial Medical Center. Patient records were crusting secondary to atrophic rhinitis was defined as crust-
evaluated for demographic data, clinical presentation, oper- ing longer than six months after completion of radiation
ative procedure, postoperative course, tumor staging, his- therapy.
topathological findings, immediate and delayed complica-
tions, rates of recurrence and metastasis, and mortality.
Olfactory neuroblastomas were staged according to the
Kadish staging system. All other malignant lesions were RESULTS
staged according to the TNM staging system for nasal
cavity and ethmoid sinus malignancies. Preoperative imag- A summary of patient data is presented in Table 1.
ing included computed tomography (CT) and/or magnetic
resonance imaging (MRI). Demographic Data/Clinical Presentation
Early in the study period, TER was considered for tu- Twenty consecutive patients underwent TER of ASB tu-
mors without significant intracranial extension and for pa- mors. Only one patient was excluded from the analysis
tients of advanced age or with significant medical comor- because he required a bifrontal craniotomy to clear the right
bidities in whom traditional CFR was believed to be too supraorbital dural margin. Of the remaining 19 patients (11
high a risk. In later years, the indications for TER were males, eight females) the mean age was 61.6 years (range
expanded to include younger and healthier patients, and 39-81 years). Significant medical comorbidities were
most ASB tumors. All ASB resections and reconstructions present in 11 patients (58%) as shown in Table 1. Nasal
were performed by a single surgeon. Image guidance was airway obstruction (68%) was the most common presenting
922 Otolaryngology–Head and Neck Surgery, Vol 136, No 6, June 2007

Figure 1 Diagram depicting the minimal extent of resection for bilateral (A) and unilateral (B) endoscopic anterior skull base resections
in the coronal and sagittal (C) planes.

Figure 2 Intraoperative photographs demonstrating an anterior skull base defect after bilateral endoscopic resection (A) and reconstruc-
tion with a single sheet of Alloderm (B). The margins of resection include the orbital walls laterally (arrows), frontal sinus anteriorly (F),
and sphenoid sinus posteriorly (S).
Dave et al Surgical outcomes and safety of transnasal . . . 923

symptom, followed by facial pain or headache (53%), epi- atively. All patients with malignant disease, excluding the
staxis (42%), visual disturbance (5%), and no symptoms two with hemangiopericytoma, and one with recurrent olfac-
(5%). tory neuroblastoma who was previously radiated, received
Three patients had a planned 2-stage procedure in which postoperative radiation therapy. One patient with small cell
the approach to the ASB and diagnostic biopsies were carcinoma also received postoperative chemotherapy.
performed first, followed by a formal ASB resection at a
second operative setting after histopathological confirma-
Recurrence/Metastases and Mortality
tion. Four patients had a planned single-stage procedure.
The mean follow-up period was 34.3 months (range 3-105
The remaining 12 patients were referred after a prior partial
months). As of the last follow-up visit, only one patient
resection in which the diagnosis of an ASB neoplasm was
(patient 4) had recurred locally. He underwent revision
obtained.
endoscopic resection for a posteroinferior septal recurrence
at 52 months after his original TER. Despite an aggressive
Operative and Perioperative Data revision resection, which included a completion septec-
The extent of resection included nine bilateral, six unilat- tomy, removal of nasopharyngeal mucosa and musculature,
eral, and four partial resections. One of the partial resections and burring of the rostrum and sphenopalatine area into the
was a revision for recurrent olfactory neuroblastoma after a pterygomaxillary space, diffuse microscopic disease was
previous CFR and postoperative radiation therapy. An en present on virtually all frozen-section specimens. The pa-
bloc resection was performed in 11 patients. The remaining tient decided against postoperative chemotherapy or further
non– en bloc resections included four unilateral resections, radiation therapy to address his recurrence. Review of the
in which a portion of the specimen was removed piecemeal initial and revision resection specimens demonstrated sev-
or burred down with a drill, and four partial resections. eral skip lesions on histopathological examination. One
The reconstruction of the resulting ASB defects is shown patient (patient 5) with recurrent olfactory neuroblastoma
in Table 1. Nine defects (47%) were reconstructed with developed regional metastases to the eyelid. Another patient
Alloderm alone. Other reconstruction techniques in- (patient 3) with HIV infection and SNUC subsequently
cluded the use of lyophilized dura and mucosal graft in developed regional and distant metastases to the neck, tem-
four patients (21%), alloderm and mucosal graft in three poral bone, and lung. These were treated with modified neck
patients (16%), mucosal graft alone in two patients dissection, postoperative radiation therapy, and palliative
(11%), and Gelfoam alone in one patient (5%). There chemotherapy. The patient subsequently died at 24 months
were no postoperative CSF leaks. postoperatively and represented the only mortality in the
The mean operative time was 245 minutes (range 153- series. The overall local control rate for all neoplasms was
405 minutes). The mean blood loss was 985 ml (range 94.7 percent and 94.1 percent for malignant disease. It
300-2400 ml). All but two patients received intraoperative should be noted that the tumor control rate may be prema-
antibiotics, and all patients received systemic antibiotics ture given the small sample size and limited follow-up.
postoperatively while in the hospital. The average hospital
stay, which included the day of surgery, was 3.7 days (range
Complications
2-9 days). Only one patient required a period of observation
Overall, there were 16 complications, which are summa-
in the ICU, which lasted two days. No patients required a
rized in Table 2. Five intraoperative complications occurred
lumbar drain or tracheotomy.
in four patients. Three patients had intraoperative bleeding
that required blood transfusion. Patient five, who underwent
Tumor Characteristics a partial ASB resection for recurrent olfactory neuroblas-
There were 17 malignant and two benign lesions. Olfactory toma, had a small unplanned CSF leak that was repaired
neuroblastoma was the most common pathology, occurring with Gelfoam. The same patient also developed an orbital
in 10 patients (53%). One recurrent olfactory neuroblastoma hematoma that required a lateral canthotomy and medial
and two benign lesions were not staged. On the basis of the orbital decompression. She did not have any permanent
Kadish staging system, there were five stage A (55%), two visual sequelae.
stage B (22%), and two stage C (22%) olfactory neuroblas- Three immediate postoperative complications occurred
tomas. Of the remaining seven malignancies, there were two in three patients, including symptomatic anemia in two
T1 (29%), one T2 (14%), two T3 (29%), and two T4 (29%) patients (patients 2 and 9), who required blood transfusion.
lesions. Three patients (patients 13, 14, and 17) had dural Overall, the perioperative transfusion rate was 26.3 percent.
involvement, and patient 7 (sarcomatous meningioma) dem- Patient 5 developed unexplained altered mental status,
onstrated intracranial involvement with an indentation of which required a 2-day admission to the ICU. She promptly
the brain parenchyma. Although all margins were cleared by improved without any permanent sequelae. There were no
intraoperative frozen-section analysis, two patients (patients perioperative mortalities.
7 and 13) demonstrated close margins of resection on per- Eight delayed postoperative complications occurred in
manent histopathological examination. Neither of these pa- five patients. Two patients (patients 2 and 9) developed
tients has had a recurrence at 12 and 35 months postoper- epistaxis requiring endoscopic cauterization, one at one
924 Otolaryngology–Head and Neck Surgery, Vol 136, No 6, June 2007

Table 1
Patient summary

Patient no./age/gender/ OR time


comorbidity Pathology/stage Resection Reconstruction (min)

1/49/F/none OFN/stage A Non–en bloc, unilateral Lyophilized dura, MT 285


mucosa
2/63/M/CAD, CHF, DM OFN/stage B En bloc, bilateral Lyophilized dura, 405
MT mucosa
3/52/M/HIV infection SNUC/stage T3 En bloc, bilateral Lyophilized dura, 375
MT mucosa
4/76/M/CAD Adenoid cystic carcinoma/ Non–en bloc, partial Septal mucosa 190
stage T2
5/81/F/none Recurrent OFN Non–en bloc, partial Gelfoam 155

6/78/F/CAD OFN/stage A Non–en bloc, unilateral MT mucosa 195


7/70/M/IDDM Sarcomatous meningioma/ En bloc, bilateral Lyophilized dura, septal 315
stage T4a bone, MT mucosa
8/52/M/HCC OFN/stage A Non–en bloc, unilateral Alloderm, septal mucosa 265
9/73/F/none Hemangio-pericytoma/ En bloc, unilateral Alloderm, mucosal graft 270
stage T3
10/69/F/CAD, IDDM Hemangio-pericytoma/ Non–en bloc, partial Alloderm, mucosal graft 153
stage T1
11/39/F/none Benign osteoblastic Non–en bloc, partial Alloderm 178
neoplasm/stage n/a
12/73/M/none OFN/stage A En–bloc, unilateral Alloderm 258
13/56/M/CAD Small cell carcinoma/ En bloc, bilateral Alloderm 330
stage T4b
14/39/M/none OFN/stage C En bloc, bilateral Alloderm 396
15/79/F/IDDM Adenoid cystic carcinoma/ En bloc, bilateral Alloderm 169
stage T1
16/45/F/MS Hemangioepithilioma/ Non–en bloc, unilateral Alloderm 240
stage n/a
17/39/M/none OFN/stage C En bloc, bilateral Alloderm 175
18/79/M/Afib OFN/stage A En bloc, bilateral Alloderm 230
19/59/M/none OFN/stage B En bloc, bilateral Alloderm 280
OR, Operative; F/U, follow-up; CAD, coronary artery disease; CHF, congestive heart failure; DM, diabetes mellitus; HIV, human
immunodeficiency virus; IDDM, insulin-dependent diabetes mellitus; HCC, hepatitis C cirrhosis; MS, multiple sclerosis; Afib, atrial
fibrillation; OFN, olfactory neuroblastoma; MT, middle turbinate; XRT, radiation therapy; SNUC, sinonasal undifferentiated carci-
noma; ICU, intensive care unit; AMS, altered mental status; n/a, not applicable.

month and the other at 40 months postoperatively. Patient plasms by Smith et al16 in 1954, and the skin incisions and
15 presented with a small linear scar in her nasal vestibule, bony cuts that were described by Ketcham in 1963 are still
presumably secondary to an intraoperative injury from en- used today. Proponents of this approach maintain that, de-
doscopic manipulation. Patients 3 and 7 developed atrophic spite significant morbidity, traditional CFR allows for a true
rhinitis and prolonged crusting, which were treated with en bloc oncological resection.1,2 Although in theory, a
transnasal irrigation, and topical and oral antibiotics with piecemeal removal may increase the rate of local recurrence
improvement. One patient (patient 2) partially extruded his through tumor seeding, this result has not been demon-
lyophilized dural graft at eight months postoperatively with- strated clinically.2,8,15 Other authors insist that a true en bloc
out a CSF leak. Patient 7 developed a frontal lobe abscess resection is rarely realized with traditional CFR given the
that required craniotomy and drainage, and subsequently limited access to certain key anatomical areas, including the
suffered radiation-induced loss of vision in his right eye. sphenoid sinus, frontal recess, nasion, and orbital apex.
Furthermore, piecemeal CFR does not appear to adversely
affect survival.1,2,8,15,17,18 More recently, the need for uni-
DISCUSSION versal resection of the entire ASB has been called into
question, and it is possible that, in select cases, unilateral
Traditional CFR through an external approach has been the and partial resections may be advisable.
gold standard for resection of ASB tumors.1,2 This approach The morbidity and mortality associated with traditional
was originally applied to the treatment of sinonasal neo- CFR is quite high. The overall major complication rate is
Dave et al Surgical outcomes and safety of transnasal . . . 925

Table 1
(continued)

Blood Hospital Adjuvant Positive margins/ F/U


loss (mL) stay (d) Complications therapy recurrence Metastasis (mo)

715 2 None XRT No/no No 105

1100 5 Transfusion, graft extrusion, epistaxis XRT No/no No 104

1500 3 Transfusion, atrophic rhinitis XRT No/no Neck, temporal 24


bone, lung
500 2 None XRT No/yes No 55

1000 92 (ICU) Intraop CSF leak, orbital hematoma, No No/no Eyelid 75


transient AMS
500 2 None XRT No/no No 18
2400 7 Transfusion, frontal lobe abscess, XRT No/no No 12
atrophic rhinitis, XRT visual loss
800 2 None XRT No/no No 55
900 5 Transfusion, epistaxis No No/no No 44

300 4 None No No/no No 44

450 2 None No No/no No 15

2000 5 Transfusion XRT No/no No 26


1000 3 None XRT chemo No/no No 35

1500 3 None XRT No/no No 10


600 4 Nasal vestibule scar XRT No/no No 10

850 3 None No No/no No 7

700 4 None XRT No/no No 5


1500 3 None XRT No/no No 3
400 4 None XRT No/no No 4

reported to be as high as 30 to 50 percent,3,4 and includes for better preservation of uninvolved structures and thus
significant intracranial, orbital, infectious, cosmetic, and limits subsequent functional morbidity compared with
systemic morbidities.1,5 Perioperative mortality has been CFR.2,15 Some potential advantages include decreased op-
reported in 0 to 13 percent of cases.2 Therefore, a less erative time, reduced anesthetic risk, shorter hospital stay,
invasive but equally effective approach would be desirable. less postoperative pain, and fewer complications.
In the 1990s, endoscopic-assisted CFR, in which the ASB is Regardless of the approach, complete tumor extirpation
approached via a bifrontal craniotomy from above and endo- is essential. Local recurrence, poor outcomes, and decreased
scopically from below, was described.1,6-8 More recently, with survival are all associated with positive surgical margins.19
advances in endoscopic technology and surgical experience, In our series, there were no positive margins. Close margins
TER for ASB tumors, which avoids the need for open of resection were demonstrated on permanent histopathol-
craniotomy, has become more prevalent.1,2,9-15 Advocates gical examination in two patients, and to date neither has
of the transnasal endoscopic method claim that the superior recurred. One patient with adenoid cystic carcinoma did
visualization with angled endoscopes and improved instru- recur, which was most likely secondary to skip lesions that
mentation allows for an oncologically sound resection with were demonstrated on both the initial and revision resection
equivocal results.1,2 Other stated advantages include avoid- specimens.
ance of craniotomy, facial, gingival, and bicoronal inci- The ability to completely remove the tumor by TER must
sions, extensive facial osteotomies, lumbar drains, trache- be assessed by thorough preoperative examination and re-
otomy, and frontal lobe retraction.1,2,5,6,8 TER also allows view of imaging. Appropriate patient selection is key. If
926 Otolaryngology–Head and Neck Surgery, Vol 136, No 6, June 2007

Table 2
and TER. For the purposes of this study, we chose to
Summary of complications consider these effects as a complication. By doing so, we
emphasized them as an outcome, because we believe they
Patient complications No. of pts may be less frequent following TER given the less extensive
resection.
Intraoperative
Blood transfusion 3 Interestingly, all 16 complications occurred in only seven
Small unplanned CSF leak 1 patients. Single complications developed in two patients
Orbital hematoma 1 (patients 12 and 15) with early stage tumors. Multiple com-
Total 5 in 4 patients
plications developed in three patients with T3 or T4 tumors
Immediate postoperative
Blood transfusion 2 (patients 3, 7, and 9), one patient with a recurrent lesion
Transient AMS 1 (patient 5), and one patient with a Kadish stage B neoplasm
Total 3 in 3 patients (patient 2). Furthermore, two major complications occurred
Delayed postoperative in a single patient with a T4a lesion (patient 7). These
Epistaxis 2
Atrophic rhinitis/crusting 2 findings suggest that certain patient factors—particularly
Nasal vestibule scar 1 advanced tumor stage—were associated with increased
Extrusion of graft 1 perioperative morbidity.
Frontal lobe abscess 1 Because adjuvant radiation therapy is not without mor-
XRT visual loss (unilateral) 1
Total 8 in 5 patients bidity, its role after TER must be elucidated. Atrophic
rhinitis, blindness, frontal lobe necrosis, and radiation-
Pts, Patients; CSF, cerebrospinal fluid; AMS, altered men-
tal status; XRT, radiation. induced malignancies are only some of the potential com-
plications. In a recent review, Bentz et al20 suggested that,
for ASB neoplasms treated by traditional CFR, postopera-
tive radiation therapy may be necessary only for tumors that
complete removal cannot be achieved, other approaches demonstrate high-grade pathology, positive margins, large
must be considered. If it is realized intraoperatively that volume of disease, or extensive local invasion (ie, dura).
surgical margins cannot be cleared by TER alone, the sur- Therefore, in select cases, traditional CFR may preclude the
geon should be prepared to either stage the procedure for a need for postoperative radiation, which is currently recom-
later date or convert to an open approach. Neurosurgical mended for all our patients in whom TER is performed for
support must be available in case an open craniotomy is malignant disease.
necessary, as was needed for the one patient who was In summary, the overall morbidity and mortality as-
excluded from this review. An endoscopic-assisted CFR is sociated with TER appear to be less than that with tra-
an option to address significant intracranial extension. For ditional CFR. There was only one significant intracranial
significant inferior extension to the floor of the nose, ante- and one significant intraorbital complication, neither of
rior extension that involves the facial soft tissues, and lateral which resulted in permanent disability. The major com-
extension to the maxillary sinus, orbit, pterygomaxillary plication rate directly related to surgery was 11 percent.
space, or infratemporal fossa, a traditional CFR is usually TER for ASB tumors requires a high degree of experi-
indicated if endoscopic resection is not possible.2,7 Endo- ence. Although not used in this series, image guidance
scopes and endoscopic instrumentation can still be used may be used, but is not necessary for most cases. Con-
with a traditional CFR to improve visualization and access
version to an external approach may be necessary; there-
to key anatomical areas.8 For tumors that are considered
fore, neurosurgical support must be available. Patients
unresectable, TER may play a role in palliation.2
with significant comorbidities and advanced age, who
Overall, 16 complications occurred in the current series.
might not otherwise tolerate an extensive CFR, appear to
Of these, we would consider only three to be major com-
be ideal candidates. In fact, our experience with TER for
plications. Two of these, the orbital hematoma and frontal
lobe abscess, were directly related to the operative proce- ASB tumors evolved from a need to treat these patients in
dure. Neither patient suffered any permanent sequelae. The whom traditional CFR was considered too high a risk.
other complication, unilateral radiation-induced loss of vi- These patients were actually referred by head and neck
sion, was a result of postoperative radiation therapy. Two oncology surgeons or neurosurgeons for a less invasive
patients developed atrophic rhinitis and prolonged crusting, endoscopic option. Although more than 30 percent of the
which was attributed to a combination of extensive mucosal tumors in this series were Kadish stage C or TNM stage
resection and radiation therapy. Both of these patients had T3/T4, less advanced tumors appear to be more amenable
advanced lesions (T3 and T4a). It should be noted that to TER and result in less postoperative morbidity. Fur-
atrophic rhinitis and prolonged crusting are more accurately thermore, unilateral and partial resections may be advis-
classified as a consequence of surgery and radiation therapy, able in certain cases. The current analysis demonstrates
rather than as a complication. In theory, both effects would that, in a select group of patients and neoplasms, the
be expected to occur at similar rates after traditional CFR short-term local control (95%) appears to be excellent.
Dave et al Surgical outcomes and safety of transnasal . . . 927

CONCLUSIONS 9. Stammberger H, Anderhuber W, Walch C, et al. Possibilities and


limitations of endoscopic management of nasal and paranasal sinus
In this preliminary review, TER for ASB tumors appears to malignancies. Acta oto-rhino-laryngologica Belgica 1999;53:199 –
205.
be safe. A larger, multi-institutional series with longer fol- 10. Walch C, Stammberger H, Anderhuber W, et al. The minimally inva-
low-up and direct comparison to CFR using patient- and sive approach to olfactory neuroblastoma: combined endoscopic and
tumor stage matched data is warranted. stereotactic treatment. Laryngoscope 2000;110:635– 40.
11. Unger F, Walch C, Stammberger H, et al. Olfactory neuroblastoma
The authors thank Brian P. Dunham, MD, for creating the (esthesioneuroblastoma): report of six cases treated by a novel com-
original illustrations in the manuscript. bination of endoscopic surgery and radiosurgery. Minim Invasive
Neurosurg 2001;44:79 – 84.
12. Cakmak O, Ergin NT, Yilmazer C, et al. Endoscopic removal of
esthesioneuroblastoma. Int J Pediatr Otorhinolaryngol 2002;64:233– 8.
REFERENCES 13. Kuhn FA, Javer AR. Low-grade fibrosarcoma of the anterior skull
base: endoscopic resection and repair. Am J Rhinol 2003;17:347–50.
1. Casiano RR, Numa WA, Falquez AM. Endoscopic resection of esthe- 14. Liu JK, O’Neill B, Orlandi RR, et al. Endoscopic-assisted craniofacial
sioneuroblastoma. Am J Rhinol 2001;15:271–9. resection of esthesioneuroblastoma: minimizing facial incisions—
2. Batra PS, Citardi MJ, Worley S, et al. Resection of anterior skull base technical note and report of 3 cases. Minim Invasive Neurosurg 2003;
tumors: comparison of combined traditional and endoscopic tech- 46:310 –5.
niques. Am J Rhinol 2005;19:521– 8. 15. Har-El G, Casiano RR. Endoscopic management of anterior skull base
3. Kraus DH, Shah JP, Arbit E, et al. Complications of craniofacial tumors. Otolaryngol Clin North Am 2005;38:133– 44.ix.
resection for tumors involving the anterior skull base. Head Neck 16. Smith RR, Klopp CT, Williams JM. Surgical treatment of cancer of the
1994;16:307–12. frontal sinus and adjacent areas. Cancer 1954;7:991– 4.
4. Richtsmeier WJ, Briggs RJ, Koch WM, et al. Complications and early 17. McCutcheon IE, Blacklock JB, Weber RS, et al. Anterior transcranial
outcome of anterior craniofacial resection. Arch Otolaryngol Head (craniofacial) resection of tumors of the paranasal sinuses: surgical tech-
Neck Surg 1992;118:913–7. nique and results. Neurosurgery 1996;38:471–9. Discussion 79 – 80.
5. Casler JD, Doolittle AM, Mair EA. Endoscopic surgery of the anterior 18. Nishino H, Miyata M, Morita M, et al. Combined therapy with con-
skull base. Laryngoscope 2005;115:16 –24. servative surgery, radiotherapy, and regional chemotherapy for max-
6. Yuen AP, Fan YW, Fung CF, et al. Endoscopic-assisted cranionasal illary sinus carcinoma. Cancer 2000;89:1925–32.
resection of olfactory neuroblastoma. Head Neck 2005;27:488 –93. 19. Patel SG, Singh B, Polluri A, et al. Craniofacial surgery for malignant
7. Yuen AP, Fung CF, Hung KN. Endoscopic cranionasal resection of skull base tumors: report of an international collaborative study. Can-
anterior skull base tumor. Am J Otolaryngol 1997;18:431–3. cer 2003;98:1179 – 87.
8. Thaler ER, Kotapka M, Lanza DC, et al. Endoscopically assisted 20. Bentz BG, Bilsky MH, Shah JP, et al. Anterior skull base surgery for
anterior cranial skull base resection of sinonasal tumors. Am J Rhinol malignant tumors: a multivariate analysis of 27 years of experience.
1999;13:303–10. Head Neck 2003;25:515–20.

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