Unusual Isolated Parapharyngeal Second Branchial Cleft Cyst: A Case Report and Literature Review.

IF 0.4 Q4 OTORHINOLARYNGOLOGY Case Reports in Otolaryngology Pub Date : 2020-12-08 eCollection Date: 2020-01-01 DOI:10.1155/2020/8814071
Emad A Magdy, Geylan A Fadali, Mahmoud Seif-Elnasr, Mohamed F Fathalla
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引用次数: 7

Abstract

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.

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罕见孤立咽旁第二鳃裂囊肿1例报告并文献复习。
第二鳃裂囊肿(BCCs)是常见的先天性颈部肿胀的原因;然而,孤立的咽旁间隙的表现是极其罕见的,只有零星的病例报道。我们在本报告中的目标是描述一个病例,并回顾当前世界文献中采用的不同诊断和管理策略。这个病例是一位26岁的女性,她有一个巨大的孤立性咽旁基底细胞癌,一直延伸到颅底,她最初的症状是耳痛和疼痛的左右头部旋转,持续了几个月,然后是咽痛。先前的计算机断层扫描(CT)怀疑咽旁脓肿。术前磁共振成像(MRI)显示一3.1 × 3.4 × 5.4 cm咽旁BCC,诊断正确。囊肿经口完全手术切除,无并发症。随访24个月无复发迹象。对过去30年所有报告病例进行全面的世界文献检索,发现23例独立病例报告中的30例采用了不同的诊断和手术方式。在这种罕见的情况下,详细讨论了表现和管理策略。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牢记BCC诊断,MRI是术前成功诊断的关键。如果遇到,经口途径可以是一种安全,美观和有效的完全手术切除方法,而不是大多数其他咽旁肿胀,通常最好通过经宫颈途径切除。
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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
自引率
0.00%
发文量
20
审稿时长
13 weeks
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