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源自斜坡胚胎残余物的鼻咽部肿物:病例系列

Nasopharyngeal Masses Arising from Embryologic Remnants of the Clivus: A Case Series.

作者信息

Sajisevi Mirabelle, Hoang Jenny K, Eapen Rose, Jang David W

机构信息

Division of Head and Neck Surgery & Communication Sciences, Department of Surgery, Duke University Medical Center, Durham, North Carolina, United States.

Deparment of Radiology, Duke University Medical Center, Durham, North Carolina, United States.

出版信息

J Neurol Surg Rep. 2015 Nov;76(2):e253-7. doi: 10.1055/s-0035-1564603. Epub 2015 Oct 25.

DOI:10.1055/s-0035-1564603
PMID:26623237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4648734/
Abstract

Objectives This study aims to (1) discuss rare nasopharyngeal masses originating from embryologic remnants of the clivus, and (2) discuss the embryology of the clivus and understand its importance in the diagnosis and treatment of these masses. Design and Participants This is a case series of three patients. We discuss the clinical and imaging characteristics of infrasellar craniopharyngioma, intranasal extraosseous chordoma, and canalis basilaris medianus. Results Case 1: A 16-year-old male patient with a history of craniopharyngioma resection, who presented with nasal obstruction. A nasopharyngeal cystic mass was noted to be communicating with a patent craniopharyngeal canal. Histology revealed adamantinomatous craniopharyngioma. Case 2: A 43-year-old male patient who presented with nasal obstruction and headache. Computed tomography (CT) and magnetic resonance imaging revealed an enhancing polypoid mass in the posterior nasal cavity abutting the clivus. Histopathology revealed chondroid chordoma. Case 3: A 4-year-old female patient with a recurrent nasopharyngeal polyp. CT cisternogram showed that this mass may have risen from a bony defect of the middle clivus suggestive of canalis basilaris medianus. Conclusions Understanding the embryology of the clivus is crucial when considering the differential diagnosis of a nasopharyngeal mass. Identification of characteristic findings on imaging is critical in the diagnosis and treatment of these lesions.

摘要

目的 本研究旨在:(1)探讨起源于斜坡胚胎残余的罕见鼻咽部肿物;(2)探讨斜坡的胚胎学并了解其在这些肿物诊断和治疗中的重要性。

设计与参与者 这是一个包含三名患者的病例系列。我们讨论了鞍下颅咽管瘤、鼻内骨外脊索瘤和基底中管的临床及影像学特征。

结果 病例1:一名16岁男性患者,有颅咽管瘤切除病史,出现鼻塞症状。发现一个鼻咽部囊性肿物与一个开放的颅咽管相通。组织学检查显示为造釉细胞瘤型颅咽管瘤。病例2:一名43岁男性患者,出现鼻塞和头痛症状。计算机断层扫描(CT)和磁共振成像显示鼻腔后部有一个强化的息肉样肿物,毗邻斜坡。组织病理学检查显示为软骨样脊索瘤。病例3:一名4岁女性患者,患有复发性鼻咽息肉。CT脑池造影显示该肿物可能起源于斜坡中部的骨质缺损,提示基底中管。

结论 在考虑鼻咽部肿物的鉴别诊断时,了解斜坡的胚胎学至关重要。识别影像学上的特征性表现对这些病变的诊断和治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/fbb81950a604/10-1055-s-0035-1564603-i150020-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/57c646f62d93/10-1055-s-0035-1564603-i150020-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/45562ad490ee/10-1055-s-0035-1564603-i150020-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/35b9122d502e/10-1055-s-0035-1564603-i150020-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/fbb81950a604/10-1055-s-0035-1564603-i150020-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/57c646f62d93/10-1055-s-0035-1564603-i150020-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/45562ad490ee/10-1055-s-0035-1564603-i150020-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/35b9122d502e/10-1055-s-0035-1564603-i150020-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb1/4648734/fbb81950a604/10-1055-s-0035-1564603-i150020-4.jpg

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本文引用的文献

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From notochord formation to hereditary chordoma: the many roles of Brachyury.从脊索形成到遗传性脊索瘤:Brachyury 的多种作用。
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The clivus: anatomy, normal variants and imaging pathology.斜坡:解剖、正常变异及影像学表现。
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