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Extradural arachnoid cyst in the thoracic spine: Case report

机译:胸椎外蛛网膜囊肿:案例报告

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BackgroundExtradural arachnoid cysts (EAC) have been described as a rare cause of spinal cord and nerve root compression, usually in the mid to lower thoracic spine and at the thoraco-lumbar junction in a posterior position. The most common theory presumes a pouch-like herniation of arachnoid through a dural defect associated to subsequent pressure fluctuations in the cerebrospinal fluid during exercise and Valsalva manoeuvres can lead to distension of the cyst and symptom aggravation.Casuistic and methodsCase report based on the retrospective analysis of the medical record and complementary exams of the patient associated with a literature review of indexed databases MEDLINE, LILACS, SciElo, BIREME, Scopus, PubMED, Cochrane Library.Clinical representationClinical History and Neurological Examination: Male patient, 24-year-old was admitted in our service complaining of back pain seen in the thoracic topography. On clinical examination, the motor strength and deep tendon reflex in the superior and inferior limbs were normal. He presented dysesthesia in the T7 level, bilaterally. Neuroimaging Investigation: On the MRI study, there is a well presented circumscribed cystic lesion in the posterior extradural space in the t7–t8 spinal levels. The lesion showed no enhancement after the gadolinium administration.Surgery and prognosticThe patient underwent a total laminectomy centred on level T7, such that the spinal cord appeared to be completely decompressed after the cystic mass was removed. Pathological examination of the cyst wall revealed that it was composed of fibrocollagenous layers with scattered meningothelial cells, such this diagnosis of EAC was adopted. During postoperative evaluation of six months, the patient evolved well without any neurological deficits up to the present.ConclusionCases of EAC represents rare etiology in the spinal differential diagnosis, such that there are around only thirty cases described in the world. Although EAC is a benign pathology, the early diagnosis and adequate neurosurgical intervention aiming to complete microsurgical cyst removal and closure of the dural defect results in excellent prognosis for these patients.
机译:背景特拉内蛛网膜囊肿(EAC)被描述为脊髓和神经根部压缩的罕见原因,通常在中间到下胸脊柱和后部位置处的胸腰带。最常见的理论假定通过与脑脊液中的脑脊液中的随后的压力波动相关的囊状突发,并且缬沙血管机动可以导致囊肿和症状恶化的障碍。基于回顾性分析关于与索引数据库的文献综述相关的患者的病历和补充考试Medline,Lilacs,Scielo,Bireme,Scopus,Pubmed,Cochrane图书馆。临床代表性杂志和神经学检查:男性患者,24岁的人被录取在我们的服务中,抱怨胸廓地形中看到的背痛。关于临床检查,优越和下肢的电机强度和深肌腱反射是正常的。他在T7水平,双边地呈现了患膜。神经影像学研究:对MRI研究,在T7-T8脊柱水平的后遮蔽空间中存在良好的囊性囊性病变。在钆给药后,病变没有增强。尿剂和预后患者在水平T7上进行的总叠层切除术,使得在除去囊性质量后脊髓似乎完全减压。囊壁的病理检查显示,它由纤维纤维神经层组成,散射脑细胞细胞,采用这种EAC的这种诊断。在术后评估六个月期间,患者在没有任何神经缺陷的情况下进化良好。EAC的组合Case代表脊髓鉴别诊断中的罕见病因,使得世界上仅有三条案例。虽然EAC是一种良性病理学,但旨在完全染色的早期诊断和足够的神经外科干预措施,对这些患者的性能缺陷的封闭产生了优异的预后。

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