Bolger W E, Woodruff W W, Morehead J, Parsons D S
Department of Otolaryngology-Head and Neck Surgery, Wilford Hall USAF Medical Center, Lackland AFB, TX 78236-5300.
Otolaryngol Head Neck Surg. 1990 Nov;103(5 ( Pt 1)):759-65. doi: 10.1177/019459989010300516.
Maxillary sinus hypoplasia is an anomaly of the paranasal sinuses occasionally encountered by otolaryngologists. Although this entity has been previously reported, an association between maxillary sinus hypoplasia and anomalies of other paranasal sinus structures, such as the uncinate process, has not yet been described. Additionally, the literature lacks a system by which the various types of maxillary sinus hypoplasia can be classified using computerized tomographic (CT) imaging. Two hundred and two consecutive coronal sinus computerized tomographic scans from patients undergoing evaluation at our institution were analyzed to determine the prevalence of MSH and associated paranasal sinus anomalies. The overall prevalence of maxillary sinus hypoplasia was 10.4%. Three distinct patterns of hypoplasia were evident. Type I, characterized by a normal uncinate process, a well-defined infundibular passage, and mild sinus hypoplasia, occurred in 14 patients (6.9%). Type II, characterized by absence or hypoplasia of the uncinate process, an ill-defined infundibular passage, and soft-tissue density opacification of a significantly hypoplastic sinus occurred in 6 patients (3.0%). Type III, characterized by absence of the uncinate process and a profoundly hypoplastic, cleft-like sinus, occurred in 1 patient (0.5%). Recognition of associated anomalies of the uncinate process in patients with maxillary sinus hypoplasia undergoing sinus surgery is of utmost clinical significance because the uncinate process serves as a key landmark during functional endoscopic sinus surgery. Failure to recognize hypoplasia or absence of the uncinate process could lead to inadvertent intraoperative damage to the adjacent medial orbital wall.
上颌窦发育不全是一种耳鼻喉科医生偶尔会遇到的鼻窦异常情况。尽管此前已有关于该病症的报道,但上颌窦发育不全与其他鼻窦结构异常(如钩突)之间的关联尚未见描述。此外,文献中缺乏一种利用计算机断层扫描(CT)成像对各种类型的上颌窦发育不全进行分类的系统。我们分析了在本机构接受评估的患者连续202例鼻窦冠状位CT扫描结果,以确定上颌窦发育不全(MSH)及相关鼻窦异常的患病率。上颌窦发育不全的总体患病率为10.4%。明显存在三种不同类型的发育不全。I型表现为钩突正常、漏斗通道清晰且鼻窦轻度发育不全,见于14例患者(6.9%)。II型表现为钩突缺如或发育不全、漏斗通道不清晰且明显发育不全的鼻窦有软组织密度影充填,见于6例患者(3.0%)。III型表现为钩突缺如且鼻窦极度发育不全呈裂隙样,见于1例患者(0.5%)。对于接受鼻窦手术的上颌窦发育不全患者,识别钩突的相关异常具有极其重要的临床意义,因为在功能性内镜鼻窦手术中,钩突是一个关键标志。未能识别钩突发育不全或缺如可能导致术中意外损伤相邻的眶内侧壁。