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斜坡骨纤维异常增殖症——病例研究与文献综述

Fibrous dysplasia of the clivus - A case study and literature review.

作者信息

Butt Aqeel, Patel Kunj, Agrawal Kanupriya, Arya Alok, Singh Jaswinder

机构信息

London North West University Healthcare NHS Trust, Ealing Hospital, Uxbridge Road, Southall UB1 3HW, United Kingdom.

Radiology Department, Watford General Hospital, Vicarage Road, Watford WD18 0HB, United Kingdom.

出版信息

Radiol Case Rep. 2020 Nov 28;16(2):230-236. doi: 10.1016/j.radcr.2020.11.019. eCollection 2021 Feb.

DOI:10.1016/j.radcr.2020.11.019
PMID:33304432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7708769/
Abstract

Fibrous dysplasia is a benign, congenital skeletal disorder which leads to the formation of fibro-osseous intramedullary bone lesions. Clival fibrous dysplasia is a rare variant which commonly presents asymptomatically with no findings on examination and is often picked up incidentally on radiological investigation. A 39-year-old female presented with a sudden onset headache of 3 days' duration alongside diplopia and right lower limb weakness upon examination. Computerized tomography head scan revealed an expansile clivus with a ground-glass appearance, magnetic resonance imaging brain scan revealed a predominantly hypointense signal on T1- and T2-weighted images and subsequent whole-body bone imaging confirmed the diagnosis of monostotic clival fibrous dysplasia. This case highlights the importance of considering monostotic clival fibrous dysplasia as a differential diagnosis in patients presenting with sudden onset symptoms of headache alongside cranial and peripheral nerve involvement, when other more sinister causes have been excluded.

摘要

骨纤维异常增殖症是一种良性先天性骨骼疾病,可导致骨髓内纤维性骨病变的形成。斜坡骨纤维异常增殖症是一种罕见的变异类型,通常无症状,检查无异常发现,常在影像学检查时偶然发现。一名39岁女性因突发头痛3天就诊,检查时伴有复视和右下肢无力。头颅计算机断层扫描显示斜坡膨胀,呈磨玻璃样外观,脑部磁共振成像扫描显示在T1加权和T2加权图像上主要为低信号,随后的全身骨成像确诊为单发性斜坡骨纤维异常增殖症。该病例强调,当排除其他更严重病因时,对于出现突发头痛症状并伴有颅神经和周围神经受累的患者,应考虑单发性斜坡骨纤维异常增殖症作为鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/7708769/a1c73f357377/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/7708769/6fb3150bbe1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/7708769/a1c73f357377/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/7708769/6fb3150bbe1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/7708769/a1c73f357377/gr4.jpg

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Fibrous dysplasia of bone: craniofacial and dental implications.骨纤维异常增殖症:颅面和牙科方面的影响。
Oral Dis. 2017 Sep;23(6):697-708. doi: 10.1111/odi.12563. Epub 2016 Sep 1.
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Endoscopic Endonasal Surgery for Uncommon Pathologies of the Sellar and Parasellar Regions.
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Adv Tech Stand Neurosurg. 2023;48:139-205. doi: 10.1007/978-3-031-36785-4_7.
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A case of intradiploic epidermoid cyst.一例板障内表皮样囊肿。
Quant Imaging Med Surg. 2023 Aug 1;13(8):5451-5455. doi: 10.21037/qims-22-1338. Epub 2023 Jun 29.
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A Rare Case of a Primary Leiomyoma of the Clivus in an Immunocompetent Patient and a Review of the Literature Regarding Clival Lesions.免疫功能正常患者中斜坡原发性平滑肌瘤的罕见病例及关于斜坡病变的文献综述
Diagnostics (Basel). 2022 Dec 21;13(1):9. doi: 10.3390/diagnostics13010009.
Acta Neurochir (Wien). 2016 Aug;158(8):1605-16. doi: 10.1007/s00701-016-2847-8. Epub 2016 Jun 8.
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