Siedler Declan G, Ibbett Imogen M, Thani Nova B
School of Medicine, Faculty of Health, University of Tasmania, Hobart, Tasmania, Australia.
Department of Neurosurgery, Royal Hobart Hospital, Hobart, Tasmania, Australia.
World Neurosurg. 2017 Mar;99:810.e5-810.e10. doi: 10.1016/j.wneu.2016.12.106. Epub 2017 Jan 3.
Intracranial hypotension secondary to spontaneous spinal cerebrospinal fluid (CSF) fistula is a rare condition that can have serious sequelae. Early diagnosis and treatment can be challenging.
We present the case of a 17-year-old male who presented with a history of sudden-onset, postural headaches associated with upper thoracic back pain. Magnetic resonance imaging (MRI) demonstrated a thoracic extradural fluid collection and slumping of the brain within the posterior fossa. The patient was initially managed with a period of bed rest, followed by a thoracic epidural blood patch. Symptoms recurred and subsequent operative exploration found a large arachnoid cyst with CSF egress through a linear split in the axilla of the right T7 nerve root. The arachnoid cyst was resected, and the defect was closed primarily. All symptoms completely resolved. MRI at 3 months postoperatively demonstrated normal spinal configuration and resolution of brain sagging.
Spontaneous CSF leaks are a rare cause of postural headache. Although epidural blood patching is an easy and safe intervention, early serial imaging to ascertain the evolution of the pathology may identify cases that are amenable to early surgical management.
自发性脊髓脑脊液漏继发颅内低压是一种罕见疾病,可导致严重后遗症。早期诊断和治疗具有挑战性。
我们报告一例17岁男性患者,其有突发、体位性头痛伴上胸背部疼痛病史。磁共振成像(MRI)显示胸段硬膜外积液及后颅窝内脑下沉。患者最初接受一段时间的卧床休息治疗,随后进行了胸段硬膜外血贴疗法。症状复发,随后的手术探查发现一个大的蛛网膜囊肿,脑脊液通过右侧T7神经根腋部的线性裂口流出。切除蛛网膜囊肿,并对缺损进行一期缝合。所有症状完全缓解。术后3个月的MRI显示脊柱形态正常,脑下垂消失。
自发性脑脊液漏是体位性头痛的罕见原因。尽管硬膜外血贴疗法是一种简单且安全的干预措施,但早期进行系列影像学检查以确定病变的演变情况,可能会识别出适合早期手术治疗的病例。