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        First branchial cleft cyst accompanied by external auditory canal atresia and middle ear malformation:A case report

        2020-09-16 13:35:10ChunLinZhangChunLeiLiHangQiChenQiangSunZhaoHuiLiu
        World Journal of Clinical Cases 2020年16期

        Chun-Lin Zhang,Chun-Lei Li,Hang-Qi Chen,Qiang Sun,Zhao-Hui Liu

        Chun-Lin Zhang,Chun-Lei Li,Hang-Qi Chen,Qiang Sun,Zhao-Hui Liu,Department of Otorhinolaryngology,Head and Neck Surgery,Affiliated Hospital of Zunyi Medical University,Zunyi 563000,Guizhou Province,China

        Hang-Qi Chen,Qiang Sun,Postgraduate College of Zunyi Medical University,Zunyi 563000,Guizhou Province,China

        Abstract

        Key words:First branchial cleft anomaly;External auditory canal atresia;Middle ear malformation;Case report

        INTRODUCTION

        First branchial cleft anomalies (FBCAs) are rare,accounting for less than 8% of all branchial anomalies in the head and neck.FBCAs are usually classified as cysts,sinuses,and fistulas according to the clinical features[1,2].In a few cases,FBCAs are accompanied by microtia,stenosis or atresia of the external auditory canal (EAC),and cholesteatoma[3-6].In this study,we report a case of FBCA accompanied by bony atresia of the EAC,middle ear malformation,as well as location malformation of the facial nerve (FN) according to the intraoperative findings.To our knowledge,this is the first report of such a complex case.An effective treatment strategy including lesion excision,mastoidectomy,and simultaneous meatoplasty and ossiculoplasty under microscopy was undertaken,which achieved a satisfactory outcome.As the cyst was closely related to the FN,we performed the cystectomy with complete preservation of the parotid gland under the microscope to better protect the FN.

        CASE PRESENTATION

        Chief complaints

        A 19-year-old male patient presented to our department in June 2019,with a mass behind the right earlobe and recurrent postauricular swelling and pain since childhood.He received abscess incision drainage three times in a local hospital.The patient also had severe hearing loss in the right ear since birth.

        History of present illness

        The patient had a mass behind the right earlobe and recurrent postauricular swelling and pain since childhood.

        History of past illness

        The patient had no other previous medical history.

        Physical examination

        A 2 cm × 3 cm fluctuant and tender mass in the postauricular area,and bony atresia of the EAC were observed.

        Laboratory examinations

        A computed tomography (CT) scan of the temporal bone showed a hypointense cystic mass protruding into the area of the atretic EAC (Figure 1).Color Doppler ultrasound showed a mucocele-like lesion with inhomogenous internal echoes.Pure-tone audiometry showed severe conductive hearing loss with an air-bone conduction gap of 56 decibels (dB).

        FINAL DIAGNOSIS

        The final diagnosis in this patient was FBCA accompanied by EAC atresia and middle ear malformation.

        Figure 1 Temporal bone computed tomography findings.A:The first branchial cleft cyst;B:The white arrow indicates the lesion tightly adhered to the facial nerve;C:The orange arrow indicates that the incus is fused with the lateral bony plank.

        TREATMENT

        Under general anesthesia,mass excision,mastoidectomy,and simultaneous meatoplasty and tympanoplasty were performed under microscopy.A postauricular incision was performed,which showed that the mass originated from the stylomastoid foramen and adhered to the posterior surface of the parotid gland,invading the temporal bone.The lesion which tightly adhered to the stylomastoid foramen segment and the vertical segment of the FN was carefully removed with complete preservation of the parotid gland.Location malformation of the FN was observed,and the vertical segment was shifted to the anteposition and embedded in the lateral atresia bony plank of the tympanic cavity.We removed the bony structure to assess the tympanic cavity,and found that the ossicular chain was fused to the bony atresia plank,the malleus and incus were fused and fixed,and the stapes was normal with a mobile footplate.Tympanoplasty was performed with the tragus cartilage and a partial ossicular replacement prosthesis.A posterior occipital tissue flap and skin flap were used for meatoplasty (Figure 2).

        OUTCOME AND FOLLOW-UP

        The patient recovered well with an open EAC and improved hearing.The postoperative air-bone conduction gap was 21 dB,and the pure-tone average gain was 35 dB (Figure 3).No evidence of recurrence was found during follow-up at 6 mo postoperatively.No major complications,such as facial palsy and significant sensorineural hearing loss,occurred.

        DISCUSSION

        Generally,FBCAs are classified into Work I and Work II types according to the anatomical and histological features[7],Type I lesions are always present as soft cysts lined by squamous epithelium,and usually protrude into the EAC.Type II lesions usually present as a cyst,sinus,or fistula and are of ectodermal and mesodermal origin,containing either skin appendages or cartilage[6,8].The histopathological examination of our case showed a soft cyst lined by squamous epithelium,the lesion was classified as Type 1,as previously reported[6],the soft mass also protruded into the bony atresia plank.

        Most structures of the head and neck originate from the differentiation of branchial arches.The first arch develops into the EAC and tympanic membrane,and abnormal differentiation can induce FBCAs and aberrations of the EAC.Generally,EAC bony atresia means that the bony atresia plank has occupied the normal structure of the EAC.FBCA accompanied by external ear diseases are rare,and to date,only a few FBCA cases accompanied by congenital EAC stenosis or atresia,and cholesteatoma have been reported[4,9-11].Banakiset al[4]reported a case of bilateral ear canal cholesteatomas in the setting of underlying FBCA.Hinsonet al[10]reported the case of a 15-year-old female with a Type II first branchial cleft cyst presenting as a right neck mass and two main facial nerve trunks were found during surgery.However,to thebest of our knowledge,this is the first report of a FBCA accompanied by EAC bony atresia,middle ear malformation and FN location malformation.The maldevelopment of the first and second branchial arches and the first gill ditch may cause malformation of the external and middle ear.

        Figure 2 Intraoperative findings and surgical strategy.A:The lesion;B:The white arrow indicates the fusion of the malleus head and incus body,the black arrow indicates that the malleus handle was fused to the lateral bony plank,the yellow arrow shows the origin of the lesion;C:The white arrow indicates the hearing reconstruction with a partial ossicular replacement prosthesis and tragus cartilage graft,the black arrow shows the location variation of the facial nerve,which migrated to the anteposition.a:The lesion;b:The atretic bony plank outside the closed tympanic cavity.In:Incus;MH:Malleus head;PG:Parotid gland;FN (t):Tympanic segment of the facial nerve;FN (v):Vertical segment of the facial nerve;LSC:Lateral semicircular canal;St:Stapes;ET:Eustachian tube.

        Figure 3 Comparison of preoperative and postoperative pure tone audiometry in the right ear.A:Shows the preoperative pure tone audiometry,the preoperative air-bone conduction gap was 56 decibels;B:Shows postoperative pure tone audiometry,the postoperative air-bone gap was 21 decibels,and the pure-tone average gain was 35 decibels.

        The diverse presentations and duplicated anomalies of FBCA pose a challenge for surgeons.As the lesions are usually very deep and often involved with the FN and parotid gland,especially in the condition of FBCA accompanied by aural stenosis or atresia,clinicians should be familiar with the otological and head and neck clinical features;surgical expertise must be available to remove the lesion completely,preserve FN function,and perform otologic reconstruction if necessary[12].Traditionally,surgical removal of a FBCA involves either superficial or total parotidectomy for exposure[13],which might cause unnecessary trauma and the risk of FN injury[6,10].Janget al[11]reported a recurrent FBCA case,in which canal wall-up mastoidectomy and lesion removal under microscopy,with an effective postauricular approach,were performed.

        CONCLUSION

        In the present case,for EAC bony atresia,a postauricular approach was chosen for mastoidectomy.During the operation,the cyst was tightly adhered to the FN and parotid gland,lesion excision under microscopy reduced the risk of FN injury with preservation of the parotid gland.Interestingly,we found that the FN vertical segment was embedded outside the atretic bony plate of the tympanic cavity,we thus performed canaloplasty and ossiculoplasty at the same time.The patient had hearing improvement after surgery.To our knowledge,this is the first report of a FBCA accompanied by EAC bony atresia,middle ear malformation and FN location malformation,which were successfully treated with FBCA lesion removal,and simultaneous meatoplasty and tympanoplasty.

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