Magdy Emad A, Fadali Geylan A, Seif-Elnasr Mahmoud, Fathalla Mohamed F
Department of Otorhinolaryngology-Head & Neck Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Department of Pathology, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Case Rep Otolaryngol. 2020 Dec 8;2020:8814071. doi: 10.1155/2020/8814071. eCollection 2020.
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.
第二鳃裂囊肿(BCCs)是颈部肿胀常见的先天性病因;然而,孤立性咽旁间隙表现极为罕见,仅有零星病例报道。本报告的目的是描述一例病例,并回顾当前世界文献中采用的不同诊断和治疗策略。所呈现的病例是一名26岁女性,患有一个巨大的孤立性咽旁BCC,延伸至颅底,最初的症状是数月的牵涉性耳痛和头部向两侧转动时疼痛,随后出现吞咽痛。之前进行的计算机断层扫描(CT)怀疑是咽旁脓肿。术前通过磁共振成像(MRI)做出了正确诊断,显示一个3.1×3.4×5.4厘米的咽旁BCC。囊肿经口完全手术切除,无并发症。24个月的随访后未发现复发迹象。对过去30年所有报道病例进行全面的世界文献检索,发现23篇单独病例报告中有30例,采用了不同的诊断和手术方式。详细讨论了此类罕见病例的表现和治疗策略。我们的研究表明,虽然罕见,但在处理孤立性咽旁间隙肿胀时应考虑BCC的诊断,MRI是术前成功诊断的关键。如果遇到这种情况,与大多数其他咽旁肿胀通常通过经颈途径更好切除不同,经口途径可以是一种安全、美观且有效的完全手术切除方法。