[Clinical features and temporal CT findings in patients with Branchio-Oto-Renal or Branchio-Oto Syndrome].

H. Yang, H. Feng, W. Lu
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Abstract

Objective: To assess the clinical features and CT diagnostic characteristics of Branchio-Oto-Renal or Branchio-Oto Syndrome. Methods: The temporal CT findings and clinical features observations of 13 patients with Branchio-Oto-Renal Syndrome (BORS) or Branchio-Oto Syndrome(BOS) confirmed by genetic testing were retrospectively analyzed. There were 8 males and 5 females, aged from 1 to 39 years, with a median age of 9 years, in which 3 pairs (6 cases) were parent-child relationship. Results: All of 13 cases had hearing loss and preauricular fistula, 11 cases accompanied by 2nd branchial fistulas. There were 20 ears of mixed hearing loss, 3 ears of sensorineural hearing loss, and 2 ears of conductive hearing loss. The mutation point of gene testing was located in EYA1 in 12 cases and SIX1 in 1 case. Twenty ears showed gradually narrowing of the diameter of basal turn, with hypoplasia in the second turn and aplasia in apical turn. There were irregular wall of vestibule and horizontal semicircular canal in 10 ears,widened vestibular in 7 ears, and vestibular fusion with horizontal semicircular canal in 3 ears. Three ears had an enlarged vestibular aqueduct, 8 ears showed enlargement of internal auditory canal. Seventeen ears had adhesion of malleolus to tympanic cavity. Six ears could not measured the incudostapedial joint angle by reason of tympanic inflammatory cover, 3 ears could not show incudostapedial joint, and 8 ears showed the incudostapedial joint angle more than 122°. Six ears showed poor oval window, and 1 ear had poor round window. Eighteen ears showed distended eustachian tube, and accompanied by tympanic or mastoiditis in 11 ears. Anterolateral shift of tympanum was found in 22 ears, 17 ears had low middle cranial fossa, and 3 ears had stenotic external auditory canal. Conclusions: Cochlear dysplasia, ossicular chain malformation and distended eustachian tube comprise the characteristic CT signs of BOS/BORS, which possesses versatile and complex CT findings. Temporal CT can accurately assess the important structures such as cochlea, ossicles, vestibule, semicircular canal, vestibular aqueduct and internal auditory canal. Combing with the clinical characteristics of bilateral, mixed hearing loss, preauricular fistula and branchial fistula can provide valuable information for early diagnosis and treatment.
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[支气管-奥托-肾脏或支气管-奥托综合征患者的临床特征和颞部 CT 发现]。
目的评估分支-奥托-肾脏或分支-奥托综合征的临床特征和 CT 诊断特点。方法: 对 13 例支奥陶肾综合征患者的时间 CT 结果和临床特征进行观察:回顾性分析13例经基因检测确诊的分支-奥托-肾脏综合征(BORS)或分支-奥托综合征(BOS)患者的颞部CT结果和临床特征。其中 8 名男性和 5 名女性,年龄在 1 至 39 岁之间,中位年龄为 9 岁,其中 3 对(6 例)为亲子关系。结果:13 例均有听力损失和耳前瘘管,11 例伴有第二支瘘管。20耳为混合性听力损失,3耳为感音神经性听力损失,2耳为传导性听力损失。基因检测的突变点位于 EYA1(12 例)和 SIX1(1 例)。20 只耳朵的基转直径逐渐变窄,第二转发育不良,顶转发育不良。10 只耳朵的前庭壁和水平半规管不规则,7 只耳朵的前庭增宽,3 只耳朵的前庭与水平半规管融合。3 只耳朵的前庭导水管扩大,8 只耳朵的内耳道扩大。17 只耳朵的耳郭与鼓室粘连。有 6 只耳朵因鼓膜炎症覆盖而无法测量入镫骨关节角度,3 只耳朵无法显示入镫骨关节,8 只耳朵显示入镫骨关节角度超过 122°。6 只耳朵的椭圆形窗口不佳,1 只耳朵的圆形窗口不佳。18 只耳朵显示咽鼓管胀大,11 只耳朵伴有鼓膜炎或乳突炎。22 只耳朵的鼓膜出现前外侧移位,17 只耳朵的中颅窝较低,3 只耳朵的外耳道狭窄。结论是耳蜗发育不良、听骨链畸形和咽鼓管扩张是 BOS/BORS 的特征性 CT 征象,其 CT 表现多样且复杂。颞部 CT 可准确评估耳蜗、听小骨、前庭、半规管、前庭导水管和内耳道等重要结构。结合双侧听力损失、混合性听力损失、耳前瘘管和支气管瘘管的临床特点,可为早期诊断和治疗提供有价值的信息。
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CiteScore
0.40
自引率
0.00%
发文量
12432
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