Sameer K S Muhammed, Mohanty Suravi, Correa Marjorie Mariam Ann, Das Kanishka
Department of Neonatal and Paediatric Surgery, St. John's Medical College Hospital, St. John's National Academy of Health Sciences, Bangalore 560034, India.
Int J Pediatr Otorhinolaryngol. 2012 Feb;76(2):165-8. doi: 10.1016/j.ijporl.2011.11.025. Epub 2011 Dec 20.
Lingual thyroglossal duct cysts (TGDC) are rare and liable to be missed in a cursory clinical examination. This study aimed to report the details of lingual TGDC from the authors' series and review existing literature on the entity.
A 12 year retrospective survey of all cases of thyroglossal duct anomalies managed at a tertiary teaching hospital was conducted to identify those with lingual TGDC. Their clinical presentation, investigations, diagnosis and management were analysed. Case series from anecdotal published English literature were critically reviewed with particular regard to diagnosis and management.
Of 78 cases of thyroglossal duct anomalies, 3 were lingual TGDC. All were females. One neonate presented with feeding difficulty and was clinically misdiagnosed as a ranula. The two older children presented with a cyst at the foramen caecum. The varied imaging and diagnostic dilemma are presented. The older children had cysts abutting the hyoid and were managed with transoral excision and a Sistrunk procedure; the neonate was managed with transoral excision only. This report also reviews the sparse literature and discusses specific issues in their treatment. The differential diagnoses encompass a wide array of developmental and neoplastic entities. Specific anatomic imaging with USG/CT/MRI and functional evaluation with radionuclide thyroid scan are essential investigative modalities. Besides a classical Sistrunk procedure and simple transoral excision, newer less invasive treatment options including marsupialisation and alcohol ablation have been reported.
In conclusion, the diagnosis and management of lingual TGDC needs to be individualised depending on their presentation and anatomic location. The Sistrunk's procedure is ideal for those in close proximity to the hyoid; however complete cyst excision would suffice in the rest.
舌甲状腺舌管囊肿(TGDC)较为罕见,在粗略的临床检查中容易被漏诊。本研究旨在报告作者系列中舌TGDC的详细情况,并回顾关于该疾病的现有文献。
对一家三级教学医院诊治的所有甲状腺舌管异常病例进行了为期12年的回顾性调查,以确定舌TGDC患者。分析了他们的临床表现、检查、诊断和治疗情况。对已发表的英文文献中的病例系列进行了严格审查,尤其关注诊断和治疗。
在78例甲状腺舌管异常病例中,3例为舌TGDC。均为女性。1例新生儿出现喂养困难,临床误诊为舌下囊肿。另外2例年龄较大的儿童在盲孔处有囊肿。展示了不同的影像学表现和诊断难题。年龄较大的儿童囊肿紧邻舌骨,采用经口切除和Sistrunk手术治疗;新生儿仅采用经口切除治疗。本报告还回顾了稀少的文献,并讨论了其治疗中的具体问题。鉴别诊断包括一系列发育和肿瘤性疾病。超声/CT/MRI等特定的解剖影像学检查和放射性核素甲状腺扫描等功能评估是必不可少的检查手段。除了经典的Sistrunk手术和简单的经口切除外,还报道了包括袋形缝合术和酒精消融术等新的微创治疗选择。
总之,舌TGDC的诊断和治疗需要根据其表现和解剖位置进行个体化。Sistrunk手术适用于那些紧邻舌骨的病例;然而,其余病例完整切除囊肿就足够了。