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酷似甲状舌管囊肿的颈支气管源性囊肿:病例报告及文献复习

Cervical bronchogenic cyst mimicking thyroglossal cyst: case report and literature review.

作者信息

Niño-Hernández Lucía Mercedes, Arteta-Acosta Cindy, Redondo-de Oro Katherine, Alcalá-Cerra Liliana, Redondo-Bermúdez César, Marrugo-Grace Olivia

机构信息

Servicio de Anatomía Patológica, Universidad de Cartagena, Colombia.

出版信息

Cir Cir. 2011 Jul-Aug;79(4):330-3.

PMID:21951887
Abstract

BACKGROUND

Bronchogenic cysts are rare congenital malformations of ventral foregut development, often with an intrathoracic location. Presentation at the cervical region is very rare.

CLINICAL CASE

We present the case of a 29-year-old female who demonstrated a 3-cm medial neck mass in relation to the hyoid cartilage. The mass was painless with a rubbery consistency, moving with tongue movements. Cervical ultrasonography and thyroid scan were suggestive of nonfunctioning thyroglossal cyst. Histopathological examination revealed the presence of a cervical bronchogenic cyst.

CONCLUSIONS

Cervical bronchogenic cyst is a rare congenital malformation that usually appears as a painless neck mass. Imaging findings are not specific for differentiating thyroid, thyroglossal, branchial or thymus cyst; therefore, clinical observation of an asymptomatic lateral neck mass in an adult should include the possibility of a bronchogenic cyst in the differential diagnosis.

摘要

背景

支气管源性囊肿是前肠腹侧发育罕见的先天性畸形,常位于胸腔内。在颈部出现极为罕见。

临床病例

我们报告一例29岁女性病例,其舌骨软骨内侧有一个3厘米的颈部肿块。该肿块无痛,质地如橡胶,随舌运动而移动。颈部超声检查和甲状腺扫描提示为无功能甲状舌管囊肿。组织病理学检查显示为颈部支气管源性囊肿。

结论

颈部支气管源性囊肿是一种罕见的先天性畸形,通常表现为无痛性颈部肿块。影像学表现对于鉴别甲状腺、甲状舌管、鳃裂或胸腺囊肿并不具有特异性;因此,对于成人无症状的侧颈部肿块进行临床观察时,鉴别诊断应包括支气管源性囊肿的可能性。

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Case report: Successful treatment of a rare case of combined parathyroid adenoma, cervical bronchogenic cyst, and tracheal diverticulum with gasless endoscopic resection of neck masses an axillary approach: A case report and literature review.病例报告:首例采用无气腋窝入路内镜下切除颈部肿物成功治疗合并甲状旁腺腺瘤、颈支气管源性囊肿及气管憩室的罕见病例:病例报告及文献综述
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Bronchogenic cyst of the neck in an elder patient: A case report.老年患者颈部支气管源性囊肿:一例报告
Int J Surg Case Rep. 2019;64:128-132. doi: 10.1016/j.ijscr.2019.10.013. Epub 2019 Oct 12.