DOI 10.1007/s00405-016-4129-8
RHINOLOGY
Abstract This study was conducted to investigate the the likelihood of encountering a mucus retention cyst
presence of the accessory maxillary ostium and its effects (48.6 %) had an approximately threefold increase, and that
on the maxillary sinus, and the concurrent occurrence of of encountering mucosal thickening (43.0 %) and maxil-
morphological variations of neighboring anatomical struc- lary sinusitis (29.1 %) had a twofold increase.
tures. This study was performed in a tertiary referral center.
This is a cross-sectional retrospective study that evaluated Keywords Paranasal sinuses Accessory maxillary ostia
coronal CTs of patients to determine the frequency of the Mucus retention cyst Sinusitis Computer tomography
accessory maxillary ostium and investigated any simulta-
neous morphological variations in neighboring anatomical Abbreviations
structures. The presence of the accessory maxillary ostium AMO Accessory maxillary ostium
(AMO) plus any concurrent morphological variations of ANC Agger nasi cells
neighboring structures were investigated in 377 patients, CT Computed tomography
with 754 sides. AMO was found to be present in 19.1 % HC Haller cells
(72/377) of the patients. A concurrent mucus retention cyst HIC Hypertrophy of inferior concha
was found to be statistically significant on both sides (right MRC Mucus retention cyst
side: p = 0.00, left side: p = 0.00), as well as mucosal MS Maxillary sinusitis
thickening (right side: p = 0.00, left side: p = 0.00), and MT Mucosal thickening
maxillary sinusitis (right side: p = 0.04, left side: PMC Pneumatization of middle concha
p = 0.03). No other concurrent variations of statistical SD Septal deviation
significance were detected in the neighboring structures.
Our study demonstrated that with the presence of AMO,
Introduction
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Mucus retention cysts 52.8–13.8 (%) (0.00**) 44.4–17.4 (%) (0.00**) 48.6–15.5 (%) (0.00**) 5.15
Mucosal thickening 41.7–17.7 (%) (0.00**) 44.4–23.9 (%) (0.00**) 43.0–20.8 (%) (0.00**) 2.87
Maxillary sinusitis 33.3–10.8 (%) (0.04*) 25–11.5 (%) (0.03*) 29.1–11.1 (%) (0.03*) 3.28
Agger nasi cell 72.2–61.6 (%) (0.27) 75–59 (%) (0.48) 73.6–60.3 (%) (0.36) 1.83
Haller cell 25–18.7 (%) (0.11) 19.4–16.1 (%) (0.20) 22.2–17.4 (%) (0.16) 1.35
Nasal septal deviation 54.1–40.6 (%) (0.37) 65.2–47.2 (%) (0.42) 59.7–43.9 (%) (0.39) 1.89
Hypertrophy of inferior 38.9–33.4 (%) (0.23) 36.1- 41.3 (%) (0.04*) 37.5–37.3 (%) (0.14) 1.00
concha
Pneumatization of middle 45.8–42 (%) (0.22) 50–46.6 (%) (0.38) 47.9–44.3 (%) (0.30) 1.15
concha
Chi-square test * p \ 0.05 ** p \ 0.001
occurrence of AMO and the agger nasi cell (right side: Pneumatization of the middle concha (PMC) was
p = 0.27, left side: p = 0. 48) (Odds Ratio=1.83) (Table 1). detected at 44.9 %. Of 144 sides in 72 patients with AMO,
Haller cells (HC) were detected at 18.3 %. Of 144 sides PMC was encountered in 47.9 % (69/144) of the sides with
in 72 patients with AMO, HC was encountered in 22.2 % 45.8 % (33/72) located on the right and 50 % (36/72) on
(32/144) of the sides, with 25 % (18/72) located on the the left side. Of 610 sides in 305 patients without AMO,
right and 19.4 % (14/72) on the left side. Of 610 sides in PMC was encountered in 44.3 % (270/610) of the patients
305 patients without AMO, HC was encountered in 17.4 % with 42 % (128/305) located on the right and 46.6 % (142/
(106/610) of the patients, with 18.7 % (57/305) located on 305) located on the left side. There was no statistical sig-
the right and 16.1 % (49/305) located on the left side. nificance for the simultaneous occurrence of AMO and the
There was no statistical significance for the simultaneous pneumatization of the middle concha (right side: p = 0.22,
occurrence of AMO and the haller cell (right side: left side: p = 0. 38) (Odds Ratio=1.15) (Table 1).
p = 0.11, left side: p = 0. 20) (Odds Ratio=1.35)
(Table 1).
Septal deviation (SD) was detected at 47.7 %. Of 144 Discussion
sides in 72 patients with AMO, SD was encountered in
60.45 % (43/72) of the sides, with 55.7 % (39/72) located Accessory maxillary ostium may be present at varying
on the right and 65.2 % (47/72) on the left side. Of 610 degrees. Several cadaver and patient studies reported that
sides in 305 patients without AMO, SD was encountered in the prevalence of accessory maxillary ostium in human
43.9 % (134/305) of the patients, with 40.6 % (124/305) beings is in the range of 0–43 % [6, 7]. The accessory is
located on the right and 47.2 % (144/305) on the left side. located at 5–10 mm superior to the attachment point of the
The simultaneous occurrence of AMO and septal deviation inferior concha and it often opens to the lateral nasal wall
was not found to be statistically significant on either side and rarely to the infundibulum. Its size is in the range of
(right side: p = 0.37, left side: p = 0.42) (Odds 1–10 mm [8]. In a study conducted by Balasubramanian in
Ratio=1.89) (Table 1). the year 2012, the accessory ostium was located in the
Hypertrophy of inferior concha (HIC) was detected at posterior side and as an elliptical shape, which can easily
37.4 %. Of 144 sides in 72 patients with AMO, HIC was be seen in routine endoscopic nasal examination [9].
encountered in 37.5 % (54/144) of the sides, with 38.9 % Genc et al. investigated the development of accessory
(28/72) located on the right and 36.1 % (26/72) on the left ostium in the year 2008 and demonstrated that accessory
side. Of 610 sides in 305 patients without AMO, HIC was maxillary ostium developed following experimentally
encountered in 37.3 % (228/610) of the patients, with induced sinusitis [2]. The incidence of accessory ostium
33.4 % (102/305) located on the right and 41.3 % (126/ appears to be higher in patients with a history of
305) located on the left side. Simultaneous occurrence of infundibular obstruction or maxillary sinus infection. This in
AMO and hypertrophy of inferior concha was found to be turn suggests that accessory ostium emerges as a result of a
statistically significant on the left side, while no such sig- pathological situation and it then stays open. Rarely, the
nificance was found for the right side (right side: p = 0.23, natural ostium itself opens directly to the middle meatus,
left side: p = 0.04) (Odds Ratio=1.00) (Table 1). i.e., the free boundary posterior to the uncinate process [10].
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into the sinus, thereby paving the way for the obstruction of 2. Genc S, Ozcan M, Titiz A, Unal A (2008) Development of
seromucous glands in the sinus and increasing retention maxillary accessory ostium following sinusitis in rabbits. Rhi-
nology 46:121–124
cyst growth. Behrbohm and Sydow demonstrated that 3. Joe JK, Ho SY, Yanagisawa E (2000) Documentation of varia-
retention cysts larger than 1.5 cm delayed mucus trans- tions in sinonasal anatomy by intraoperative nasal endoscopy.
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a role in chronic sinus etiology and the mucociliary 4. Jones NS (2002) CT of the paranasal sinuses: a review of the
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cluded that reduced mucociliary activity increases retention sinusitis. Am J Rhinol 11:361–369
cyst growth while the growth of retention cyst reduces 6. Kuma RH, Kaka RS (2001) Accessory maxillary ostia: topogra-
phy and clinical application. J Anat Soc India 50:3–5
mucociliary activity; hence, a vicious cycle is created. 7. Jog M, McGarry GW (2003) How frequent are accessory sinus
Our finding of pneumatization of the middle concha is ostia? J Laryngol Otol 117:270–272
also supported by the study of Stallmann et al. who also 8. Youngs R, Evans K, Watson M (2005) The paranasal sinuses. A
demonstrated the rate of pneumatization of the middle handbook of applied surgical anatomy. Taylor & Francis, London
9. Balasubramanian T (2012) Advanced anatomy of lateral nasal
concha as 44 % [21]. wall: for the endoscopic sinus surgeon. Otolaryngol Online J
Although there are several studies about maxillary sinus Rhinol 2:4–9
anatomy and its variations, there are no clinical studies 10. Zinreich SJ (1998) Functional anatomy and computed tomogra-
investigating whether these variations have an association phy imaging of the paranasal sinuses. Am J Med Sci 316:2–12
11. Matthews BL, Burke AJ (1997) Recirculation of mucus via
with accessory maxillary ostium or not. In that respect, our accessory ostia causing chronic maxillary sinus disease. Oto-
study brings a novel approach to the literature. laryngol Head Neck Surg 117:422–423
12. Albu S (2010) Symptomatic maxillary sinus retention cysts:
should they be removed? Laryngoscope 120:1904–1909
13. Hadar T, Shvero J, Nageris BI et al (2000) Mucus retention cyst
Conclusion of the maxillary sinus: the endoscopic approach. Br J Oral
Maxillofac Surg 38:227–229
It was identified that the presence of accessory maxillary 14. Wang JH, Yong JJ, Lee BJ (2007) Natural course of retention
ostium is associated with an approximate threefold increase cysts of the maxillary sinus: long-term follow-up results.
Laryngoscope 117:341–344
in the incidence of mucus retention cysts and a nearly 15. Busaba NY, Kieff D (2002) Endoscopic sinus surgery for
twofold increase in mucosal thickening and maxillary inflammatory maxillary sinus disease. Laryngoscope
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cysts, the distortion of mucociliary activity secondary to 16. Harar RP, Chadha NK, Rogers G (2007) Are maxillary mucosal
cysts a manifestation of inflammatory sinus disease? J Laryngol
accessory ostium and the consequent obstruction of sero- Otol 121:751–754
mucous glands in the sinus account for the combination of 17. Kanagalingam J, Bhatia K, Georgalas C et al (2009) Maxillary
accessory maxillary ostium and retention cysts. mucosal cyst is not a manifestation of rhinosinusitis: results of a
prospective three-dimensional CT study of ophthalmic patients.
Compliance with ethical standards Laryngoscope 119:8–13
18. Bhattacharyya N (2000) Do maxillary sinus retention cysts reflect
Funding source, financial disclosures None. obstructive sinus phenomena? Arch Otolaryngol Head Neck Surg
126:1369–1371
Conflict of interest None. 19. Hong SL, Cho KS, Roh HJ (2014) Maxillary sinus retention cysts
protruding into the inferior meatus. Clin Exp Otorhinolaryngol
7:226–228
20. Behrbohm H, Sydow K (1991) Nuclear medicine studies of the
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