基底性阴道与奇亚里I型形和大西洋轴不稳定:一个罕见的病例报告
Nandini Sanjay1, Chandan Y S2, Krishan Yadav2
1Orthopaedics, Sri Devaraj Urs Academy of Higher Education and Research, Kolar, IND.
Cureus
|September 27, 2023
概括
这项研究详细介绍了一例罕见的基底发育 (BI) 和Chiari I型形 (CM-I) 病例,该病例发生在36岁的男性身上. 患者表现出复杂的症状和成像发现,突出了需要个性化治疗方法的需要.
科学领域:
- 神经外科 神经外科
- 放射学 放射学是一门学科.
- 整形外科 整形外科 整形外科
背景情况:
- 基底发育 (BI) 和Chiari I型形 (CM-I) 是罕见的椎结 (CVJ) 异常.
- 这些条件影响骨底部和部部区域,呈现出不同的临床和放射性特征.
研究的目的:
- 呈现一种罕见的CM-I和相关的C1-C2异常的基础发育病例.
- 讨论这样复杂的心血管形的诊断和管理挑战.
主要方法:
- 一个36岁的男性的病例报告,持续有摇的感觉.
- 临床检查显示小脑体征,鼻,以及部运动受限.
- 放射性成像 (MRI/CT) 来评估心血管解剖学,包括BI,CM-I和C1-C2融合/不稳定性.
主要成果:
- 图像检测证实了基底阴道与显著的大脑桃体 (~14.7毫米) 和增加的atlantodens间隔 (6毫米).
- 意想不到的发现包括C1-C2的融合和不稳定性,C1入大孔.
- 患者表现出双边小脑征兆,阴囊,以及部运动受限.
结论:
- 这一案例突出了基底性发育,Chiari I型形和先天C1-C2融合与不稳定性的罕见结合.
- 对于这种复杂的心血管异常,已建立的治疗算法尚未明确,需要个性化的方法.
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