Zhang Chun-Lin, Li Chun-Lei, Chen Hang-Qi, Sun Qiang, Liu Zhao-Hui
Department of Otorhinolaryngology, Head and Neck Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou Province, China.
World J Clin Cases. 2020 Aug 26;8(16):3616-3620. doi: 10.12998/wjcc.v8.i16.3616.
We report a rare case of first branchial cleft anomaly (FBCA) accompanied by bony atresia of the external auditory canal, middle ear malformation, and location malformation of the facial nerve according to the intraoperative findings.
A 19-year-old male patient presented to our department with a mass behind the right earlobe and recurrent postauricular swelling and pain since childhood, he also had severe hearing loss in the right ear since birth. The patient underwent surgery including mass removal, mastoidectomy, and simultaneous meatoplasty and ossiculoplasty under microscopy. No facial palsy or recurrence was noted during postoperative follow-up.
FBCAs are rare, and to our knowledge, this is the first report of FBCA accompanied by external auditory canal bony atresia, middle ear malformation, and location malformation of the facial nerve. An effective postauricular approach under microscopy facilitated complete lesion removal and simultaneous otologic reconstruction.
根据术中发现,我们报告一例罕见的第一鳃裂畸形(FBCA),伴有外耳道骨性闭锁、中耳畸形和面神经位置畸形。
一名19岁男性患者因右耳垂后肿物及自幼反复耳后肿胀疼痛就诊于我科,自出生起右耳也有严重听力损失。患者接受了手术,包括肿物切除、乳突切除术,并在显微镜下同时进行外耳道成形术和听骨链成形术。术后随访期间未发现面瘫或复发。
FBCA罕见,据我们所知,这是首例伴有外耳道骨性闭锁、中耳畸形和面神经位置畸形的FBCA报告。显微镜下有效的耳后入路有助于彻底切除病变并同时进行耳科重建。