Nasal craniopharyngioma: case report and literature review

被引:9
|
作者
Magill, J. C. [1 ]
Ferguson, M. S. [1 ]
Sandison, A. [2 ]
Clarke, P. M. [1 ]
机构
[1] Charing Cross Hosp, Dept Otolaryngol Head & Neck Surg, London W6 8RF, England
[2] Charing Cross Hosp, Dept Histopathol, London W6 8RF, England
来源
JOURNAL OF LARYNGOLOGY AND OTOLOGY | 2011年 / 125卷 / 05期
关键词
Nose; Pathology; Craniopharyngioma; RECURRENCE; CHILDREN;
D O I
10.1017/S0022215110002938
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: We report the first case in the English language literature of an adamantinomatous infrasellar craniopharyngioma, and we describe our management strategy. Case report: A 46-year-old woman presented with a six-month history of left-sided nasal obstruction and epistaxis. Rhinological examination revealed a left-sided, polypoidal lesion lying medial to the middle turbinate. An urgent examination under anaesthesia was organised; biopsies were considered characteristic of craniopharyngioma. Magnetic resonance imaging and computed tomography demonstrated a well defined, heterogeneous, infrasellar mass centred in the midline, extending anteriorly into the left nasal cavity and posteriorly encasing both internal carotid arteries. Craniofacial resection was performed via a midfacial degloving approach, with adjuvant radiotherapy. The patient was disease-free one year post-operatively. Conclusion: Craniopharyngiomas should be considered in the differential diagnosis of a unilateral nasal polyp. Although technically benign, they are locally aggressive. Therefore, we recommend complete excision with adjuvant radiotherapy if margins are involved or close.
引用
收藏
页码:517 / 519
页数:3
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