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舌下囊肿:先天性还是后天性?

Plunging ranula: congenital or acquired?

机构信息

Department of Otolaryngology-Head and Neck Surgery, Manukau DHB, Manukau City, New Zealand.

出版信息

Otolaryngol Head Neck Surg. 2010 Jan;142(1):104-7. doi: 10.1016/j.otohns.2009.10.014.

Abstract

OBJECTIVE

To review our clinical experience with plunging ranula and examine the evidence in support of our impression that plunging ranula has a genetic basis.

STUDY DESIGN

Case series with chart review.

SETTING

Secondary otolaryngology service.

SUBJECTS AND METHODS

Review of the medical records of a clinical series of 80 consecutive plunging ranulas in 77 patients was conducted, with recording of clinical and radiological findings, surgical treatment, and outcome. A literature review using MEDLINE and OLD MEDLINE was performed.

RESULTS

The majority of plunging ranulas had no intraoral component on clinical examination, although evidence of mucus extravasation from the sublingual gland could be found both radiologically and histologically in all cases. There were four patients with bilateral plunging ranula and one instance of siblings with unilateral plunging ranula. Maoris and Polynesians comprised more than 82 percent of our cases; this was a significant overrepresentation of these ethnic groups (P < 0.0001). A very strong predominance of cases of Chinese origin was also evident in the literature.

CONCLUSION

The clinical findings and the supporting data from the literature, when viewed in light of information relating to the known anatomical anomaly of a dehiscence in the mylohyoid muscle and ectopic sublingual gland lying below the plane of the mylohyoid, appear to support the case for a genetic basis for this unusual clinical entity.

摘要

目的

回顾我们对陷入性舌下囊肿的临床经验,并探讨支持我们的印象,即陷入性舌下囊肿具有遗传基础的证据。

研究设计

病例系列和图表回顾。

设置

二级耳鼻喉科服务。

受试者和方法

对 77 例 80 例连续陷入性舌下囊肿的临床系列病例进行了病历回顾,记录了临床和影像学发现、手术治疗和结果。使用 MEDLINE 和 OLD MEDLINE 进行了文献回顾。

结果

大多数陷入性舌下囊肿在临床检查中没有口腔内成分,但在所有病例中都可以在影像学和组织学上发现舌下腺粘液外渗的证据。有 4 例双侧陷入性舌下囊肿和 1 例单侧陷入性舌下囊肿的兄弟姐妹。毛利人和波利尼西亚人占我们病例的 82%以上;这是这些族裔群体的显著代表性(P < 0.0001)。文献中也明显显示出华人病例的强烈优势。

结论

鉴于已知的解剖异常,即下颌舌骨肌的裂缝和位于下颌舌骨肌平面下方的异位舌下腺,临床发现和文献中的支持数据似乎支持这种不寻常的临床实体具有遗传基础的说法。

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