Service de Radiologie, Hôpital d'Enfants Armand-Trousseau, Paris, France.
Pediatr Radiol. 2011 May;41(5):652-7. doi: 10.1007/s00247-010-1913-2. Epub 2010 Dec 8.
Analysis of the middle ear with fetal MRI has not been previously reported.
To show the contribution of fetal MRI to middle ear imaging.
The tympanic cavity was evaluated in 108 fetal cerebral MRI examinations (facial and/or cerebral malformation excluded) and in two cases, one of Treacher Collins syndrome (case 1) and the other of oculo-auriculo-vertebral (OUV) spectrum (case 2) with middle ear hypoplasia identified by MRI at 27 and 36 weeks' gestation, respectively.
In all 108 fetuses (mean gestational age 32.5 weeks), the tympanic cavity and T2 hypointensity related to the ossicles were well visualised on both sides. Case 1 had micro/retrognathia and bilateral external ear deformity and case 2 had retrognathism with a left low-set and deformed ear. MRI made it possible to recognize the marked hypoplasia of the tympanic cavity, which was bilateral in case 1 and unilateral in case 2. Both syndromes are characterized by craniofacial abnormalities including middle ear hypoplasia, which cannot be diagnosed with US.
The middle ear cavity can be visualized with fetal MRI. We emphasize the use of this imaging modality in the diagnosis of middle ear hypoplasia.
胎儿 MRI 对中耳的分析尚未见报道。
展示胎儿 MRI 对中耳成像的贡献。
在 108 例胎儿颅脑 MRI 检查(排除面部和/或颅脑畸形)中评估鼓室[1],并在 2 例分别患有特雷彻·柯林斯综合征(病例 1)和眼-耳-脊椎(OUV)综合征(病例 2)的胎儿中评估鼓室[1]。这 2 例胎儿的中耳发育不全均由 MRI 在 27 周和 36 周妊娠时发现。
在所有 108 例胎儿(平均胎龄 32.5 周)中,双侧鼓室和与听小骨相关的 T2 低信号均能很好地显示。病例 1 表现为小颌/后缩和双侧外耳畸形,病例 2 表现为后缩和左侧低位及畸形耳。MRI 能够识别出鼓室明显的发育不全,病例 1 为双侧,病例 2 为单侧。这两种综合征的特征均为包括中耳发育不全在内的颅面异常,这是 US 无法诊断的。
胎儿 MRI 可显示中耳腔。我们强调了这种影像学方法在诊断中耳发育不全中的应用。