Puget Stéphanie, Kondageski Charles, Wray Alison, Boddaert Nathalie, Roujeau Thomas, Di Rocco Federico, Zerah Michel, Sainte-Rose Christian
Department of Pediatric Neurosurgery, Hôpital Necker-Enfants Malades, Paris, France.
J Neurosurg. 2007 Jan;106(1 Suppl):48-52. doi: 10.3171/ped.2007.106.1.48.
The authors describe the case of a 12-year-old girl with Marfan syndrome, sacral dural ectasia, and tonsillar herniation, who presented with headache. Initially, it was hypothesized that the headaches were secondary to the tonsillar herniation, and the patient consequently underwent surgical decompression of the foramen magnum. Postoperatively, the patient's condition did not improve, and additional magnetic resonance (MR) imaging demonstrated evidence of a cerebrospinal fluid (CSF) leak at the level of the dural ectasia. It was surmised that the girl's symptoms were due to spontaneous intracranial hypotension (SIH) and that the tonsillar herniation was caused by the leakage. The patient responded well to application of a blood patch at the level of the demonstrated leak, and her headache resolved. This appears to be the first reported case of a patient with Marfan syndrome presenting with a symptomatic spontaneous CSF leak complicated by tonsillar herniation. In this rare association of SIH and connective tissue disorders, recognition of the clinical signs and typical MR imaging features of SIH may lead to more appropriate and less invasive treatment, potentially avoiding surgery.
作者描述了一名患有马凡综合征、骶部硬脊膜膨出和扁桃体疝的12岁女孩的病例,该女孩出现头痛症状。最初,推测头痛是由扁桃体疝继发引起的,因此患者接受了枕骨大孔减压手术。术后,患者的病情并未改善,进一步的磁共振成像显示在硬脊膜膨出水平存在脑脊液漏。据推测,该女孩的症状是由于自发性颅内低压(SIH)所致,而扁桃体疝是由脑脊液漏引起的。在显示漏液的部位应用血补丁后,患者反应良好,头痛症状得以缓解。这似乎是首例报道的患有马凡综合征且出现有症状的自发性脑脊液漏并伴有扁桃体疝的患者。在这种罕见的SIH与结缔组织疾病的关联中,认识到SIH的临床体征和典型的磁共振成像特征可能会带来更恰当且侵入性更小的治疗方法,有可能避免手术。