Frontal recess anatomy in Japanese subjects and its effect on the development of frontal sinusitis: computed tomography analysis
© Kubota et al. 2015
Received: 11 November 2014
Accepted: 19 May 2015
Published: 29 May 2015
Comprehensive understanding of frontal recess anatomy is essential for the successful treatment of patients with frontal sinus disease. This study was designed to determine the prevalence of specific frontal recess cells in Japanese subjects and the association of these cells with the development of frontal sinusitis.
Frontal recess anatomy was analyzed using high-resolution spiral computed tomography images of paranasal sinuses from December 2008 through September 2011. The distribution of various frontal recess cells in patients with and without frontal sinusitis was compared by logistic regression analysis.
A total of 150 patients met the criteria, and 300 sides were analyzed. Agger nasi cells were present in 88.0 % of sides; frontal cell types 1 (FC1), 2 (FC2), 3 (FC3), and 4 (FC4) were present in 37.0 %, 6.3 %, 4.3 %, and 1.3 %, respectively; supraorbital ethmoid cells in 6.0 %, suprabullar cells in 37.0 %, frontal bullar cells (FBC) in 7.0 %, and interfrontal sinus septal cells in 8.6 %. Multiple logistic regression analysis showed that the presence of FBCs was significantly associated with the development of frontal sinusitis (p = 0.043).
The frequencies of frontal recess cells in Japanese adult patients were similar to those reported for other East Asian adult populations, including Chinese, Korean, and Taiwanese. Anatomically, FBCs may show a greater association with the development of frontal sinusitis than other frontal recess cells.
Although CT has been used to assess frontal recess pneumatization patterns [1–7], few studies in English have focused on Japanese adult populations. This study used high-resolution CT images to analyze Japanese patients with frontal sinusitis. We hypothesized that Stammberger’s theory may apply to the development of frontal sinusitis, and paid particular attention to FC3s, FC4s, SBCs, SOECs, and FBCs, which can narrow the ventilation pathway of the frontal sinus. The purpose of this study was to clarify the association of various frontal recess cells with the development of frontal sinusitis in Japanese patients by determining cell frequency in those with and without frontal sinusitis.
The study was performed at the Department of Otorhinolaryngology–Head and Neck Surgery, Hiroshima University Hospital, Hiroshima, Japan. Between December 2008 and September 2011, 150 consecutive patients underwent CT of the nasal cavities and paranasal sinuses. Spiral CT scans of the nasal cavities and paranasal sinuses were performed on a Toshiba Aquilion CT scanner (Toshiba Medical Systems, Tokyo, Japan) with 1-mm-thick axial cuts. The following scanning parameters were used: kV 120, mA 200, window level 2000, central level 500. The CT data were reconstructed into coronal and sagittal images at a computer workstation. Imaging angles, contrast, and brightness were adjusted on the computer workstation to improve bony detail, which was especially useful for identifying severely diseased frontal recess cells in patients with rhinosinusitis.
Data for 150 patients undergoing computed tomography
Frontal sinusitis (+)
Frontal sinusitis (−)
Age (years ± SEM)
57.8 ± 13.8
41.3 ± 17.5
47.0 ± 19.4
51.1 ± 18.4
Lund-Mackay score (±SEM)
7.9 ± 2.4
5.5 ± 1.8
0.19 ± 0.64
2.6 ± 3.6
Anterior ethmoid score (±SEM)
1.8 ± 0.45
1.4 ± 0.55
0.025 ± 0.16
0.58 ± 0.84
Statistical analyses were performed using Excel Statistics 2010 (Shakai Jouhou Corp. Tokyo, Japan). Multivariate logistic regression analyses were performed to identify factors associated with frontal sinusitis. The odds ratio (OR) and 95 % confidence interval (CI) were calculated for each factor. ANCs, FC1–FC4s, SBCs, SOECs, FBCs, and IFSSCs were chosen as predictive variables. A p value <0.05 was considered statistically significant for all measurements. The protocol was approved by ethical committee of epidemiological research at Hiroshima University (No. 1063).
A total of 300 sides from 150 patients were assessed (Table 1). Seventy sides, 50 from men and 20 from women, showed evidence of frontal sinusitis, whereas 230 sides did not. The mean symptom score of patients with frontal sinusitis was 2.5 ± 1.38 and the Lund–Mackay score of their frontal sinuses was 1.2 ± 0.69 (Fig. 3). Fourteen patients (14 sides) had unilateral frontal sinusitis and 28 (56 sides) had bilateral frontal sinusitis. Patients with frontal sinusitis were older (57.8 ± 13.8 years) than those without frontal sinusitis (41.3 ± 17.5 years), but the difference was not significant (p = 0.469). Mean Lund–Mackay score (7.9 ± 2.4 vs. 5.5 ± 1.8, p = 0.000) and mean anterior ethmoid score (1.8 ± 0.45 vs. 1.4 ± 0.55, P = 0.001) were significantly higher in patients with than without frontal sinusitis.
Incidence of frontal recess cells in various populations
Our cases Japanese; 300 sides, no. (%)
Taiwanese; 363 sides, no. (%)
Chinese, 404 sides, no. (%)
Korean, 114 sides, no. (%)
Caucasian, 82 sides, no. (%)
Statistical analysis of the effect of various frontal recess cells on the development of frontal sinusitis
CRS (+) 100 sides, no. (%)
CRS (−) 200 sides, no. (%)
95 % CI
95 % CI
The frontal recess is a complex space that resembles an inverted funnel or cone, with the apex at the frontal ostium. This space is filled by various anterior ethmoid or frontal recess cells . Because of the intrinsic anatomic complexity of this narrow space, comprehensive knowledge of frontal recess anatomy is required prior to surgery.
In investigating the prelavence of frontal recess cells on CT images, we found that the prevalence of ANCs was 88.0 %, similar to previous findings [1–4]. Although we found that the prevalence of FC1s in Japanese patients was almost as high as in Caucasians, the prevalence of other frontal cells (FC2–FC4s), especially FC2s, was in line with findings in other Asian populations. FC4s are independent of the appearance of ANCs . Previous studies have reported FC4s in 16 (2.1 %) of 768 subjects  and in 3 (3.1 %) of 98 frontal recesses , making FC4s quite rare among frontal recess cells. In our study, nearly half (48.9 %) of the Japanese subjects had frontal cells.
Similar to findings in other East Asian populations, SBCs were more frequent while SOECs were less frequent, in Japanese than in Caucasian patients [1–4]. Although the prevalence of these frontal recess cells in our study population was more consistent with those in Chinese, Korean, and Taiwanese populations than with those in Caucasians, the prevalence of FC1s (37.0 %) in Japanese patients was closer to that in Caucasians (35.4 %) than in Taiwanese (21.5 %), Chinese (24.4 %), and Korean (22.8 %) groups. The latter discrepancy may be due to racial differences between Japanese and other East Asian populations .
The pathophysiology of frontal sinusitis is associated with ventilation of the sinus via the sinus ostium. The size of the frontal sinus ostium is key to frontal sinus drainage. Generally, frontal recess cells and their inflammation can influence frontal sinus ventilation by narrowing the frontal sinus drainage pathway. Because frontal cells may be associated with frontal sinus inflammation, we assessed whether frontal recess cells were associated with frontal sinusitis in Japanese subjects.
The association between the presence of anterior frontal recess cells (ANCs and FC1–FC4s) and the development of frontal sinusitis is unclear. Enlargement of ANCs has been found to correlate with a decrease on CT in the anterioposterior size of the nasofrontal recess, involved in the frontal sinus drainage pathway. The association between a requirement for revision sinus surgery in patients with frontal sinusitis and agger nasi disease was highly statistically significant. Failure to address agger nasi disease can contribute to failure of the primary surgery . An analysis of 768 coronal CT scans showed that the prevalence of frontal mucosal thickening was higher in individuals with frontal cells of any type than in individuals without frontal cells, with the prevalence of FC3 and FC4 differing significantly .
Another study, however, found no difference in the frequency of frontal sinusitis on sides with and without frontal cells . Moreover, the incidence of frontal sinusitis was not increased in patients with persistent ANCs undergoing revision surgery, and the diameters and areas of the frontal isthmus were similar in sinuses with various types of frontal cells.
In assessing the frontal recess cells posterior and posterolateral to the frontal recess (FBCs, SBCs, SOECs), our multivariate analysis suggested that the prevalenc of FBCs was associated with the development of frontal sinusitis. FBCs are characterized by pneumatization along the skull base in the posterior frontal recess and extend through the frontal ostium into the true frontal sinus. FBCs are significantly associated with the narrow anteroposterior diameter of the frontal ostium and frontal recess . In frontal recesses that have FBCs, this anatomic tendency may play a role in narrowing the frontal sinus drainage pathway, resulting in significant obstruction.
Although anatomic variations in the frontal recess are likely to play a role in frontal sinusitis, mucosal inflammatory processes are also likely to be an important etiologic factor [6, 11, 12]. Allergies, asthma, and tobacco smoking can affect the nasal mucosa and lead to poorer outcomes of functional endoscopic sinus surgery, despite meticulous handling of the frontal ostium mucosa and preservation of the natural outflow tract . An evaluation of 289 frontal recesses at the time of revision surgery found that 193 (66.8 %) had mucosal edema or polyposis obstructing the frontal recess . In the absence of anatomic reasons for obstruction, mucosal inflammatory disease in the frontal recess should be considered a medical rather than a surgical problem. Seven major factors were associated with frontal sinusitis: mucosal disease (67 %); retained ethmoid cells (53 %); lateralized middle turbinates (30 %); retained ANCs (13 %); scar tissue (12 %); retained frontal cells (8 %); and neo-osteogenesis (7 %), with most frontal recesses having more than one factor (average 1.6) . Frontal sinusitis is therefore caused by multiple factors, including anatomic variations, mucosal inflammation, and sinonasal polyposis. Further investigations are needed to understand the effects of anatomic variants of frontal recess cells on frontal sinusitis.
The frequencies of frontal recess cells in Japanese adult patients were similar to those reported for other East Asian adult populations, including Chinese, Korean, and Taiwanese patients. Frontal bullar cells may have more influence on the development of frontal sinusitis than other frontal recess cells.
Written informed consent was obtained from the patient for the publication of this report and any accompanying images.
We thank Ms. Ai Kashima for her technical assistance.
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