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一名患有特发性颅内高压的儿科患者发生硬膜穿刺后头痛。

Post dural puncture headache in a pediatric patient with idiopathic intracranial hypertension.

作者信息

Nafiu Olubukola O, Monterosso Dominic, Walton Sarah R, Bradin Stuart

机构信息

Department of Anesthesiology, University of Michigan, Ann Arbor, MI 48109-0048, USA.

出版信息

Paediatr Anaesth. 2005 Sep;15(9):778-81. doi: 10.1111/j.1460-9592.2004.01529.x.

Abstract

We describe the occurrence of postdural puncture headache (PPDH) in an adolescent with idiopathic intracranial hypertension (IIH) and its successful management with an epidural blood patch. PPDH is a very rare occurrence in patients with intracranial hypertension and is described as a paradoxical situation in the literature. There are only two previous case reports (in adults) of the possible association. A 15-year-old obese patient with a diagnosis of IIH had an uneventful diagnostic spinal tap using a 22G Quincke needle in the pediatric emergency department but returned 24 h later with PPDH. After a failed trial of conservative management, she had an uneventful but curative epidural blood patch with 15 ml of autologous venous blood and was able to return to school the day after the blood patch. Follow-up review by her neuro-ophthalmologist shows resolution of her headaches, considerable improvement in her visual field defect and resolution of papilledema. This is the first report of PPDH and its successful management with an epidural blood patch in a pediatric patient with IIH.

摘要

我们描述了一名患有特发性颅内高压(IIH)的青少年发生硬膜穿刺后头痛(PPDH)的情况,以及通过硬膜外血贴成功治疗的过程。PPDH在颅内高压患者中非常罕见,在文献中被描述为一种矛盾的情况。此前仅有两例(成人)可能存在关联的病例报告。一名诊断为IIH的15岁肥胖患者在儿科急诊科使用22G Quincke针进行了一次顺利的诊断性腰椎穿刺,但24小时后因PPDH复诊。保守治疗尝试失败后,她接受了一次顺利且治愈性的硬膜外血贴,注入15毫升自体静脉血,血贴后第二天就能返校。她的神经眼科医生的随访复查显示,她的头痛症状消失,视野缺损有显著改善,视乳头水肿消退。这是关于PPDH及其通过硬膜外血贴成功治疗一名患有IIH的儿科患者的首例报告。

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