Atypical Clival Chordoma in an Adolescent without Imaging Evidence of Bone Involvement

被引:0
作者
Hashim, Hilwati [1 ]
Rosman, Azmin Kass [2 ]
Aziz, Aida Abdul [3 ]
Roqiah, Abdul Kadir [1 ]
Bakar, Nor Salmah [4 ]
机构
[1] Univ Teknol MARA, Jalan Hosp, Fac Med, Imaging Unit, Sungai Buloh 47000, Selangor, Malaysia
[2] Jalan Hosp, Sungai Buloh Hosp, Dept Neurosurg, Sungai Buloh 47000, Selangor, Malaysia
[3] Jalan Hosp, Sungai Buloh Hosp, Dept Radiol, Sungai Buloh 47000, Selangor, Malaysia
[4] Univ Teknol MARA, Jalan Hosp, Fac Med, Dept Pathol, Sungai Buloh 47000, Selangor, Malaysia
来源
MALAYSIAN JOURNAL OF MEDICAL SCIENCES | 2014年 / 21卷 / 05期
关键词
magnetic resonance imaging; adolescent; clivus; chordoma; atypical;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Clival chordoma is a rare primary bone tumour that arises from the remnant of the notochord and typically occurs in older adults. Upon imaging, the tumour can be seen arising from the clivus and causes clival destruction. This usually provides insight for a diagnosis. Here we present a case of a non-enhancing, pre- pontine mass that was hypointense on T1W and hyperintense on T2W in an adolescent. No clival bone erosion was observed. Based on the age group, imaging findings, and lack of clival erosion, a provisional diagnosis of epidermoid cyst was made and the tumour was resected. This patient was eventually diagnosed with a clival chordoma based on histopathological examination.
引用
收藏
页码:78 / 82
页数:5
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