Case Reports in Otolaryngology最新文献

{"title":"Unusual Isolated Parapharyngeal Second Branchial Cleft Cyst: A Case Report and Literature Review.","authors":"Emad A Magdy, Geylan A Fadali, Mahmoud Seif-Elnasr, Mohamed F Fathalla","doi":"10.1155/2020/8814071","DOIUrl":"10.1155/2020/8814071","url":null,"abstract":"<p><p>Second branchial cleft cysts (BCCs) are common congenital causes of neck swellings; however, isolated parapharyngeal space presentation is extremely rare, with only sporadic cases reported. Our objectives in this report are to describe a case and review different diagnostic and management strategies adopted in the current world literature. The case presented is a 26-year-old female with a large isolated parapharyngeal BCC extending to skull base in which first presenting symptoms were referred otalgia and painful side-to-side head rotation for months followed by odynophagia. A previously ordered computed tomography (CT) scan suspected a parapharyngeal abscess. Correct diagnosis was preoperatively achieved using magnetic resonance imaging (MRI) showing a 3.1 × 3.4 × 5.4 cm parapharyngeal BCC. Cyst was completely surgically excised transoral without complications. No evidence of recurrence has been noted after 24-month follow-up. A comprehensive world literature search for all reported cases in the last 30-years revealed thirty cases in 23 separate case reports with different diagnostic and surgical modalities adopted. Presentation and management strategies in such rare cases are discussed in detail. Our study shows that although rare, BCC diagnosis should be kept in mind while dealing with isolated parapharyngeal space swellings with MRI being key for successful preoperative diagnosis. If encountered, the transoral route can be a safe, aesthetically pleasing and effective way for complete surgical excision in contrast to most other parapharyngeal swellings, which are usually better excised via a transcervical approach.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8814071"},"PeriodicalIF":0.6,"publicationDate":"2020-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744222/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38762395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Efficacy of Arytenoidectomy after Suture Lateralisation Failure in Patients with Bilateral Vocal Cord Paralysis.","authors":"Shinsuke Suzuki,&nbsp;Takechiyo Yamada","doi":"10.1155/2020/8822164","DOIUrl":"https://doi.org/10.1155/2020/8822164","url":null,"abstract":"<p><strong>Background: </strong>Endolaryngeal suture lateralisation is an ideal operation for bilateral vocal fold paralysis. However, restenosis owing to breakage and slippage of suture can sometimes occur. In such a case, methods that are more effective in expanding the glottis, including arytenoidectomy, must be selected. <i>Case Report</i>. Herein, we report two female patients aged 86 and 54 years who presented with bilateral vocal cord paralysis and who had restenosis after suture lateralisation. Endoscopic partial arytenoidectomy was performed, and satisfactory outcomes were obtained. This method maintains the height of the arytenoid and preserves its sensation by leaving a part of the cartilage and mucous membrane.</p><p><strong>Conclusion: </strong>Endoscopic partial arytenoidectomy is effective for securing the airway while preserving vocal function and preventing aspiration. This technique is suitable for patients with restenosis after they have undergone endolaryngeal suture lateralisation.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8822164"},"PeriodicalIF":0.6,"publicationDate":"2020-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676922/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38676346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Rare Case of Fungal Necrotising Otitis Externa Centred on the Left Temporomandibular Joint.","authors":"A Khan, E Omakobia, S Hasnie, R Barton, P Gopalan, V Oktseloglou, I Smith","doi":"10.1155/2020/8874754","DOIUrl":"10.1155/2020/8874754","url":null,"abstract":"<p><strong>Introduction: </strong>Necrotising otitis externa (NOE) is a rare life-threatening complication of simple otitis externa which can be difficult to diagnose and manage. It is very rarely centred on the temporomandibular joint (TMJ). Fungi cause NOE in approximately 5-20% of patients, and a high index of suspicion is required for diagnosis, particularly when there is no improvement with prolonged topical and intravenous antibiotic therapy.</p><p><strong>Objective: </strong>To report a novel case of fungal NOE centred on the left TMJ in an immunocompromised adult male with a focus on investigations and optimal management. <i>Case Report</i>. A 67-year-old male with comorbid chronic renal impairment presented to our otolaryngology department with prolonged left otalgia and otorrhoea. Subsequent cross-sectional imaging demonstrated left NOE centred on the TMJ. Poor resolution with prolonged courses of systemic and topical anti-pseudomonal antibiotics prompted maxillofacial surgical input for left TMJ exploration, washout, and biopsy from the joint capsule. The causative organism was identified as <i>Aspergillus flavus</i> on PCR analysis. The patient was successfully treated with oral posaconazole and repeated topical insertions of amphotericin B-soaked ribbon gauze to the left ear. <i>Discussion</i>. A combination of various imaging modalities including CT, MRI, Tc-99, and gallium-67 are utilised in clinical practice both to diagnose NOE and subsequently monitor disease progression or resolution. Immunocompromised patients with confirmed fungal NOE may require a combination of treatments including surgical debridement and prolonged antifungal therapy for a number of months, if not lifelong, treatment. Initiating empirical antifungal therapy may be justified in some patients. However, this should be judged on a case-by-case basis and guided by discussion with the local microbiology and infectious diseases departments. However, there is no national guideline or consensus regarding treatment of these patients, especially in cases of fungal NOE.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8874754"},"PeriodicalIF":0.4,"publicationDate":"2020-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7665930/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38720790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"CO₂ Laser Division of Neo-Vallecula Improves Dysphagia in the Postlaryngectomy Patient: A Case Series and Review of the Literature.","authors":"Mohamad Z Saltagi,&nbsp;Chelsey A Wallace,&nbsp;Avinash V Mantravadi,&nbsp;Michael W Sim","doi":"10.1155/2020/4015201","DOIUrl":"https://doi.org/10.1155/2020/4015201","url":null,"abstract":"<p><strong>Objectives: </strong>To review the literature on neo-vallecula diagnosis and management and to report our findings regarding 3 patients who developed neo-vallecula in the context of free-flap pharyngeal reconstruction following total laryngectomy.</p><p><strong>Methods: </strong>This case series reports three patients who developed a neo-vallecula following a laryngectomy and free-flap pharyngeal reconstruction. All three patients were treated with a CO₂ laser endoscopic procedure.</p><p><strong>Results: </strong>Neo-vallecula formation is thought to be related to tension on the neopharyngeal closure or closure technique following total laryngectomy. Diagnosis may be obtained with swallow studies, videofluoroscopy, or endoscopy. Treatment has included external excision and endoscopic procedures such as stapling, harmonic scalpel excision, and laser removal. We utilized an endoscopic approach entailing the use of a CO₂ laser to divide the neo-vallecula, and all our patients reported improvement in their dysphagia.</p><p><strong>Conclusions: </strong>Treatment of an anterior neo-vallecula endoscopically using a CO₂ laser is an effective way to treat dysphagia in patients following total laryngectomy with free-flap pharyngeal reconstruction.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"4015201"},"PeriodicalIF":0.6,"publicationDate":"2020-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/4015201","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38657980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Accidental Explantation of a Cochlear Implant in a Child Who Developed Cholesteatoma as a Late Complication of Cochlear Implantation.","authors":"Wong Kein Low,&nbsp;Wan Ni Pok,&nbsp;Win Nie Ng,&nbsp;Judy Tan","doi":"10.1155/2020/6353706","DOIUrl":"https://doi.org/10.1155/2020/6353706","url":null,"abstract":"<p><strong>Introduction: </strong>Although rare, cholesteatoma can develop as a late complication of cochlear implantation. The electrode array may then be exposed in the external auditory canal surrounded by cholesteatoma debris. <i>Case Report</i>. The cochlear implant of a child was inadvertently explanted by a clinician during a routine aural toilet procedure. The child had previously reported recurrent ear infections, pain, and unexplained implant function degradation. Reimplantation was carried out 2 days later with good postoperative hearing results. Part of the electrode array was observed to be embedded in cholesteatoma. Postreimplantation recovery was complicated by a breakdown of the blind-sac. <i>Discussion</i>. Clinical indicators that could alert the clinician to the possibility of this late complication include recurrent infections, presence of keratotic debris in the external auditory canal, unexplained implant function degradation, and nonauditory stimulation. Although this patient managed to achieve excellent postreimplantation hearing outcomes, a delay in reimplantation surgery following explantation could possibly compromise successful reinsertion of the electrode array. External ear canal overclosure without mastoid cavity obliteration has merit in facilitating CT scan surveillance, but it may increase the risk of the blind-sac breaking down. This case also illustrated how the electrode array could have facilitated propagation of the cholesteatoma from the middle ear to the mastoid.</p><p><strong>Conclusion: </strong>If aural toilet is required in the implanted ear of a cochlear implant recipient, any complaint of hearing change, pain, or discharge should alert the clinician of the possibility of cholesteatoma developing. It warrants prompt evaluation by an experienced otologist in order to prevent accidental explantation. <i>Keywords</i>. Cochlear implant, cochlear implant complications, chronic suppurative otitis media, cholesteatoma, reimplantation, blind-sac, external auditory canal overclosure, mastoid cavity obliteration.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"6353706"},"PeriodicalIF":0.6,"publicationDate":"2020-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/6353706","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38657981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Rare and Unexpected Reason for Unilateral Epistaxis: Nasal Septal Schwannoma.","authors":"Alper Yenigun,&nbsp;Yasin Kulaksiz,&nbsp;Tugce Esen Kiran,&nbsp;Erol Senturk,&nbsp;Fadlullah Aksoy,&nbsp;Orhan Ozturan","doi":"10.1155/2020/4369620","DOIUrl":"https://doi.org/10.1155/2020/4369620","url":null,"abstract":"<p><p>Nasal septal schwannoma is a rare tumor. It causes complaints such as nasal congestion, nosebleeds, and headaches. There are many diseases such as nasal polyps, antrochoanal polyp, chronic rhinosinusitis, concha bullosa, inverted papilloma, and retention cyst with schwannoma diagnosis. The diagnosis is made histopathologically, and the treatment is surgery. In this case report, we presented a male patient with septal schwannoma who had nasal obstruction for a year and reviewed the last 20 years of literature on nasal schwannoma.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"4369620"},"PeriodicalIF":0.6,"publicationDate":"2020-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/4369620","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38528415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Bilateral Traumatic Facial Paralysis with Hearing Impairment and Abducens Palsy.","authors":"Imane Ouhbi,&nbsp;Taoufik Abdellaoui,&nbsp;Noureddine Errami,&nbsp;Fouad Benariba","doi":"10.1155/2020/8843187","DOIUrl":"https://doi.org/10.1155/2020/8843187","url":null,"abstract":"<p><p>The temporal bone is often affected in basilar skull fractures. Fractures involving the petrous portion are particularly significant, as they may be associated with neurovascular sequelae. Bilateral facial paralysis secondary to bilateral temporal bone fracture is a rare clinical entity, even more so when associated with other cranial nerve damage such as abducens nerve paralysis and hearing impairment. Only 4 similar cases have been reported in the literature to date. In this paper, we describe a 28-year-old male patient with bilateral facial paralysis, unilateral abducens palsy, and bilateral hearing loss due to bitemporal fractures that developed after a motor vehicle accident. Conservative management was preferred. The 6-month follow-up showed remarkable improvement. This report highlights the effectiveness of conservative management in posttraumatic complete facial and abducens palsy.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8843187"},"PeriodicalIF":0.6,"publicationDate":"2020-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8843187","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38614355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Abducens Nerve Paralysis Induced by a Primary Solitary Sphenoid Sinus Mucocele with Broad Osseous Thinning at the Cranial Base.","authors":"Shoji Naito,&nbsp;Hidenori Yokoi,&nbsp;Yuma Matsumoto,&nbsp;Michitsugu Kawada,&nbsp;Kohei Inomata,&nbsp;Masachika Fujiwara,&nbsp;Arisa Ohara,&nbsp;Koichiro Saito","doi":"10.1155/2020/8897868","DOIUrl":"https://doi.org/10.1155/2020/8897868","url":null,"abstract":"<p><p>Primary solitary sphenoid sinus mucocele is rare, generally presenting with headaches or eye symptoms at the anatomical site. We report the case of a 39-year-old woman incidentally diagnosed with sphenoid sinus mucocele during a complete medical checkup. Imaging revealed that the cystic wall had developed from the rear sphenoid sinus and had spread expansively to diminish the clivus; however, no symptoms were reported, and the patient was managed with close observation. During the follow-up period, diplopia developed suddenly due to isolated left-sided abducens nerve paralysis. An endoscopic endonasal approach was used to open the frontal cystic wall, and fascia lata and fat were used for cranial base reinforcement to avoid future cerebrospinal fluid leakage, resulting in improvement during the early stages of follow-up. Treatment options for sphenoid sinus mucoceles include close observation or surgery. In our case, we chose surgery because of an acute symptomatic manifestation during observation.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8897868"},"PeriodicalIF":0.6,"publicationDate":"2020-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8897868","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38341025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Transoral Laser-Assisted Total Laryngectomy: Expanding the TLM's World.","authors":"Aslan Ahmadi,&nbsp;Saleh Mohebbi,&nbsp;Masoud Kazemi,&nbsp;Ayda Sanaei","doi":"10.1155/2020/8827139","DOIUrl":"https://doi.org/10.1155/2020/8827139","url":null,"abstract":"<p><strong>Introduction: </strong>The introduction of laryngeal transoral procedures has created a shift in the treatment of laryngeal cancers towards the primary surgical management of patients. In this study, we aimed to evaluate the safety, efficacy, and feasibility of the transoral laser-assisted total laryngectomy (TLM-TL) in advanced laryngeal cancer. <i>Case presentation</i>. In this case report, we describe a case of a 50-year-old male patient presented to the otorhinolaryngology clinic with a history of hoarseness and odynophagia since 6 months. Based on the pathological and imaging findings, the diagnosis of stage IVa laryngeal squamous cell carcinoma with the involvement of the base, tongue, and left palatine tonsil was made for the patient, and transoral total laryngectomy with partial glossectomy via the TLM technique was planned.</p><p><strong>Result: </strong>The tumor was successfully resected by TLM-TL with clear surgical margins. No complication was observed after the surgery. Good functional recovery was obtained regarding swallowing and speech. The patient's oncologic and functional outcomes were evaluated for 2 years. Everything was satisfactory with good long-term cosmetic and laryngopharyngeal functional outcome and no sign of tumor recurrence.</p><p><strong>Conclusions: </strong>TLM-TL is a minimally invasive and cost-benefit endoscopic surgical procedure feasible in advanced laryngeal cancer with good long-term oncological and functional outcome. It could limit postoperative complications, mainly the incidence of pharyngocutaneous fistulae. It is also associated with better satisfaction after TL due to cosmetic benefits.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"8827139"},"PeriodicalIF":0.6,"publicationDate":"2020-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8827139","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38494771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Doxycycline Sclerotherapy of a Cervical Cystic Hygroma: A Caribbean Institution Experience.","authors":"Nicholas Figaro, Robbie Rampersad, Solaiman Juman","doi":"10.1155/2020/9187205","DOIUrl":"10.1155/2020/9187205","url":null,"abstract":"<p><p>Cervical cystic lymphangiomas are rare benign tumors that pose a formidable challenge to surgeons confronted with managing this uncommon entity. Due to the intimacy with which these cystic lesions blend with critical cervical structures, a considerable number of patients who undergo surgical management are often plagued with recurrence and morbidity. As a result, doxycycline sclerotherapy has become an attractive, safe, and effective alternative as a primary treatment modality in a select group of pediatric patients. This case report presents an 18-month-old patient with a large cervical cystic hygroma that was effectively treated with exclusive doxycycline sclerotherapy.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2020 ","pages":"9187205"},"PeriodicalIF":0.6,"publicationDate":"2020-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7512093/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38453036","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}