*Department of Surgery, Division of Otolaryngology-Head and Neck Surgery, †Department of Radiology, Section of Neuroradiology, ‡Department of Surgery, Division of Otolaryngology-Head and Neck Surgery, Section of Otology and Neurotology, University of Wisconsin Hospital and Clinics; and §Waisman Center, University of Wisconsin-Madison, Madison, Wisconsin, U.S.A.
Otol Neurotol. 2014 Jan;35(1):91-6. doi: 10.1097/MAO.0b013e3182a03522.
To determine if radiologic chronic otitis media (COM), both with and without cholesteatoma, is associated with superior semicircular canal dehiscence (SSCD).
Retrospective review of consecutive high-resolution computed tomography (HRCT) scans of the temporal bone.
Tertiary care medical center.
Two hundred consecutive patients undergoing HRCT of the temporal bone beginning January 1, 2012.
Imaging was evaluated by 3 reviewers (2 neuroradiologists and 1 neurotologist). All scans were assessed for the presence of SSCD, cholesteatoma, chronic otomastoiditis, tegmen dehiscence, and for abnormalities of the cochlea, vestibule, facial nerve, and temporal bone vasculature.
Ears with COM associated with chronic otomastoiditis or cholesteatoma were compared with those without COM with respect to the presence of SSCD or other temporal bone abnormalities. Statistical analysis was performed to assess for differences between the groups studied.
One-hundred ninety-four patients (388 ears) were included. Cholesteatoma was identified in 48 ears (12.4%) and chronic otomastoiditis in 62 ears (16%). Ten ears with cholesteatoma had ipsilateral SSCD, and 8 ears with chronic otomastoiditis had ipsilateral SSCD. In 340 ears without either cholesteatoma or chronic otomastoiditis, SSCD was found in 18 (5.3%). SSCD was found to occur significantly more often in patients with ipsilateral radiologic cholesteatoma. No cases of SSCD were associated with cochlear, facial nerve, or vascular abnormalities.
Our findings suggest that COM with cholesteatoma is associated with the presence of SSCD, although the nature of this association is unclear.
确定是否放射学慢性中耳炎(COM),伴有或不伴有胆脂瘤,与上半规管裂(SSCD)有关。
回顾性分析连续高分辨率 CT(HRCT)颞骨扫描。
三级医疗中心。
2012 年 1 月 1 日起连续 200 例接受 HRCT 颞骨的患者。
由 3 名审阅者(2 名神经放射科医生和 1 名神经耳科医生)对影像学进行评估。所有扫描均评估 SSCD、胆脂瘤、慢性乳突炎、天幕裂、耳蜗、前庭、面神经和颞骨血管的异常。
比较伴有慢性乳突炎或胆脂瘤的 COM 耳与无 COM 耳的 SSCD 或其他颞骨异常的存在情况。对两组进行统计学分析,以评估两组之间的差异。
纳入 194 例患者(388 耳)。48 耳(12.4%)发现胆脂瘤,62 耳(16%)发现慢性乳突炎。10 耳胆脂瘤同侧有 SSCD,8 耳慢性乳突炎同侧有 SSCD。在 340 例无胆脂瘤或慢性乳突炎的耳中,18 耳(5.3%)发现 SSCD。同侧放射学胆脂瘤患者 SSCD 发生率明显较高。无 SSCD 与耳蜗、面神经或血管异常相关。
我们的研究结果表明,伴有胆脂瘤的 COM 与 SSCD 的存在有关,尽管这种关系的性质尚不清楚。