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外中耳畸形伴咽鼓管全程扩大畸形的CT表现

CT features of abnormally whole-course wide eustachian tubes with microtia and atresia

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目的 探讨外中耳畸形伴咽鼓管全程扩大畸形患者的CT特征.方法 该研究为横断面研究,回顾性分析2017年1月至2021年12月复旦大学附属眼耳鼻喉科医院19例(20耳)外中耳畸形伴咽鼓管全程扩大畸形患者的临床特征和CT影像学资料,其中男15例、女4例,年龄5~16岁,平均9.5岁.选取50例外中耳畸形但咽鼓管无扩大患者(男32例、女18例,年龄5~16岁,平均9.2岁)作为外中耳畸形对照组,另外选取20例(40耳)因耳鸣、耳痛等就诊、耳部CT正常的患者(男12例、女8例,年龄5~16岁,平均12.5岁)作为耳部CT正常对照组.测量患者及正常对照组CT影像上咽鼓管骨性段横径、长度、咽鼓管总长度、软骨段与骨性段夹角、软骨段与水平面夹角,并应用SPSS 27.0软件进行统计分析和比较.结果 根据扩大咽鼓管与鼓室的关系将外中耳畸形伴咽鼓管全程扩大患者分为相通组和不通组,二组均显示男性好发、左侧好发,半面短小畸形发生率高等特点.CT表现为咽鼓管呈长管状含气管腔,11耳(相通组4耳,不通组7耳)咽鼓管在颅底区分叉,上部骨管向前上延伸至蝶骨体,下部向下延续为咽鼓管软骨段,沟通鼻咽腔,6耳伴蝶骨体乳突样气房.咽鼓管全程扩大患者中耳畸形程度较咽鼓管无扩大的外中耳畸形对照组更严重,尤其是不通组;相通组中耳炎发生率低于对照组,4例不通组患者曾患扩张咽鼓管炎症.与耳部CT正常对照组相比,咽鼓管扩大畸形组患者骨性段较长,而总长度较短,不通组尤甚;骨性段与软骨段角度缩小、软骨段与水平面角度增大,差异均有统计学意义(P值均<0.05).结论 外中耳畸形伴咽鼓管全程扩大畸形较为少见,男性好发、左侧好发,患侧半面短小畸形发生率高,中耳畸形程度较普通外中耳畸形更严重,尤其是与鼓室不通组;相通组中耳炎发生率明显低于普通外中耳畸形患儿,不通组可能伴扩张咽鼓管炎症.
Objective To study the clinical and CT features of the abnormal whole-course wide of eustachian tube(AWWET)with microtia and atresia(MA).Methods The clinical and CT data of 19 patients(20 ears)from January 2017 to December 2021 with AWWET with MA were retrospectively analyzed,including 15 males and 4 females.The age ranged from 5 to 16 years,with an average of 9.5 years.50 patients with common MA without wide eustachian tube(ET)as a case control group,including 32 males and 18 females.The age ranged from 5 to 16 years,with an average of 9.2 years.20 patients(40 ears)who had normal ear CT for tinnitus,otalgia as a normal control group,including 12 males and 8 females.The age ranged from 5 to 16 years,with an average of 12.5 years.We measured the dimension and length of the bony portion of the ET,the total length,the angle between the bony portion and the cartilage portion,and the horizontal angle of ET on CT imagings,and compared with 40 normal ears by SPSS 27.0 software.Results According to the relationship between AWWET and tympanum,patients were divided into the communicated group and the blocked group.A male predominance,left ear predominance,with high incidence of hemifacial microsomia exhibited in both groups.AWWET was presented as a widened lumen on CT.In 11 ears(4 ears in the communicated group,7 ears in the blocked group),ETs bifurcated,the upper bony tube extended to the sphenoid body,the lower part continued down to cartilaginous ET and opened onto the nasopharynx,with"mastoid-like"pneumatization of the sphenoid body in 6 ears.The middle ear deformity in case group was more serious than MA control group,especially the blocked group.The incidence of otitis media in the communicated group was lower than that in the MA control group,and 4 cases in the blocked group had effusion in the ET.Compaired with normal ear,the bony ET elongated significantly in the AWWET groups,and the whole course of ET was significantly shortened,specially in the blocked group.The angle between the bony ET and the cartilaginous ET was decreased and the horizontal angle of the ET increased in the AWWET groups,the difference was considered to indicate statistical significance(P<0.05).Conclusions AWWET with MA is rare,a male predominance,left ear predominance,and with high incidence of hemifacial microsomia.The middle ear deformity is more serious than common MA,especially in the blocked group.The incidence of otitis media in the communicated group is significantly lower than that in the common MA,and the blocked group may be accompanied by ET inflammation.

Eustachian tubeCongenital abnormalitiesMicrotia and atresiaTomography,X-Ray computed

刘俊华、张放、沙炎

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复旦大学附属眼耳鼻喉科医院放射科,上海 200031

咽鼓管 先天畸形 外中耳畸形 体层摄影术,X线计算机

2024

中华耳鼻咽喉头颈外科杂志
中华医学会

中华耳鼻咽喉头颈外科杂志

CSTPCD北大核心
影响因子:1.727
ISSN:1673-0860
年,卷(期):2024.59(2)
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