Difficulties in diagnosing Kimerly’s anomaly (own clinical observation)

Q4 Medicine
D. Khapchenkova, S. Dubyna, S.S. Skorobogach, V. Husiev
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引用次数: 0

Abstract

Kimmerle’s anomaly is characterized by the presence of a bony arch of congenital or secondary origin in the structure of the first cervical vertebrae, which restricts the movement of the vertebral artery and causes its compression. This pathology belongs to craniovertebral malformations - congenital anatomical defects of the structure of the junction of the skull with the first cervical vertebra. Kimerly’s anomaly is diagnosed in approximately 12-30% of the population, causing vertebral artery syndrome, which is the cause of chronic ischemia in the posterior parts of the brain. Purpose - to describe the clinical case of Kimmerle’s anomaly in a teenager as an example of a long diagnostic search for this pathology. Clinical case. A 9-year-old girl complained of frequent headaches accompanied by vomiting. Similar conditions occurred every 3-4 weeks. Gastroenterological and neurological factors were not detected. The conditions were relieved by sleep, and drug therapy was not effective. During puberty, such attacks became less frequent and later disappeared. At the age of 16, the girl began to complain of neck pain, recurrent migraines, sharp «shooting» pain in the ear, accompanied by a buzzing sound, ringing, later joined by syncopal states, gait instability, and facial muscle weakness. An X-ray of the craniovertebral junction revealed Kimmerle’s anomaly. The patient’s condition improved with the use of the Shantz collar and constant physical therapy and neuroprotective therapy. Conclusions. Kimmerle’s anomaly can be asymptomatic and incidental, but in younger patients with a combination of neuro-otolaryngological symptoms and drop attacks, this pathology should be excluded. When taking anamnesis, attention should be paid to the chronology and conditions of symptom onset, as well as the patient’s medical history. The research was carried out in accordance with the principles of the Helsinki Declaration. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
诊断Kimerly异常的困难(自己的临床观察)
Kimmerle畸形的特征是第一节颈椎结构中存在先天性或继发性骨弓,这限制了椎动脉的运动并导致其受压。这种病理属于颅骨畸形——颅骨与第一颈椎交界处结构的先天性解剖缺陷。Kimerly异常在大约12-30%的人群中被诊断为导致椎动脉综合征,这是大脑后部慢性缺血的原因。目的-描述一例青少年Kimmerle异常的临床病例,作为长期诊断该病理学的一个例子。临床病例。一名9岁女孩抱怨经常头痛并伴有呕吐。类似的情况每3-4周发生一次。未检测到胃肠道和神经系统因素。睡眠缓解了病情,药物治疗无效。在青春期,这种攻击变得不那么频繁,后来就消失了。16岁时,女孩开始抱怨颈部疼痛、反复发作的偏头痛、耳朵剧烈的“射击”疼痛,并伴有嗡嗡声、铃声,后来又出现合眼状态、步态不稳定和面部肌肉无力。颅椎交界处的X光片显示Kimmerle畸形。通过使用Shantz项圈以及持续的物理治疗和神经保护治疗,患者的病情有所改善。结论。Kimmerle异常可能是无症状和偶然的,但对于伴有神经耳鼻喉科症状和跌倒发作的年轻患者,应排除这种病理学。在进行回忆时,应注意症状发作的时间和条件,以及患者的病史。这项研究是根据《赫尔辛基宣言》的原则进行的。进行研究获得了患者的知情同意。提交人没有宣布任何利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
50
审稿时长
8 weeks
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