Al Sukhun Jehad, El Naggar Mohamad
Department of Oral Maxillofacial Surgery.
Department of Ear Nose and Throat, MedCare Hospital, Dubai, United Arab Emirates.
J Craniofac Surg. 2019 Sep;30(6):1772-1773. doi: 10.1097/SCS.0000000000005506.
Second branchial cleft cysts (BCCs) are the most common type of branchial abnormalities and usually found high in the neck. Oropharyngeal presence of a BCC is very rare. The authors report a rare case of oropharyngeal, second branchial, multilocular, cleft cyst in a 9-year-old child (8.0 × 5.0 cm in maximum diameter). The cyst was removed completely via extra/intraoral approach and did not have tract-like structure. The anatomic location together with the histopathology results, which showed a squamous epithelium-lined cystic wall with lymphoid aggregation, were characteristic findings of a BCC. Patient was discharged without any complication, and a regular follow-up of 6 months showed no evidence of recurrency. Having reviewed the literature, it seems to be that this is the first case to be reported of a multilocular BCC, excised of this size, from the oropharyngeal area in a child. Other pathological lumps of the neck have similar presentation with BCC, which makes it difficult, sometimes, to reach an accurate diagnosis. Clinicians should be aware of this pathology because it can be easily misdiagnosed as an odontogenic cyst and/or salivary gland infection, especially if it develops high up in the neck.
第二鳃裂囊肿(BCCs)是最常见的鳃源性异常类型,通常位于颈部较高位置。口咽部出现BCC非常罕见。作者报告了一例罕见的9岁儿童口咽部第二鳃裂多房性囊肿(最大直径8.0×5.0cm)。该囊肿通过口外/口内联合入路完全切除,且无条索状结构。其解剖位置以及组织病理学结果显示囊壁内衬鳞状上皮并伴有淋巴样聚集,这些都是BCC的特征性表现。患者出院时无任何并发症,6个月的定期随访未发现复发迹象。查阅文献后发现,这似乎是首次报道的从儿童口咽部区域切除的如此大小的多房性BCC病例。颈部的其他病理性肿块与BCC有相似表现,这有时使得准确诊断变得困难。临床医生应了解这种病理情况,因为它很容易被误诊为牙源性囊肿和/或唾液腺感染,尤其是当它在颈部较高位置发生时。