Isolated Anterior Extradural Enterogenous Cyst of the Thoracic Spine Mimicking an Anterior Thoracic Meningocele: A Case Report.

Surya Prakash Rao Voleti, Apurve Parameswaran, Ranjith Mahesh Nellore, Raja Shekar Kaitepalli, Vidya Kedarisetti
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Abstract

Introduction: Enterogenous cysts (also known as neurenteric cysts) are rare congenital lesions presumed to arise from an abnormal persistent communication between embryonic ectodermal and endodermal tissues. They may be symptomatic or asymptomatic, and generally have an insidious and prolonged clinical course. They are typically intradural and extramedullary in location. Very few cases of extramedullary enterogenous cysts have been reported in the literature, most of which were cranial. We present a rare case of an anteriorly situated extradural enterogenous cyst at the level of the thoracic spine, mimicking an isolated anterior thoracic meningocele on radiologic evaluation.

Case report: A 4-year-old boy was referred to our spine surgery unit for the evaluation and management of an incidentally detected T1 vertebral anomaly. Magnetic resonance imaging revealed the presence of a focal defect over the right half of the T1 vertebral body, through which herniation of a fluid-filled sac into the pre- and right paravertebral regions was noted. A diagnosis of anterior thoracic meningocele was made, and surgery was advised. Following surgical exposure of the entire extent of the sac, needle aspiration to decompress the lesion was performed, which yielded a milky-colored viscous fluid, unlike cerebrospinal fluid. The likelihood of an enterogenous cyst was suspected. The lesion was excised at the level of the base of its peduncle, and the vertebral defect was closed using a small contoured plate. Histopathologic evaluation confirmed the presence of an enterogenous cyst.

Conclusion: Anterior thoracic meningoceles and enterogenous cysts of the spine may be indistinguishable on radiologic evaluation, and a definitive diagnosis may be reached only through histopathologic evaluation. The possibility of an enterogenous cyst must be considered in the differential diagnosis of meningoceles, and vice versa.

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孤立的胸椎前硬膜外肠内生囊肿与胸前脑膜膨出相似:1例报告。
简介:肠源性囊肿(也称为神经性囊肿)是一种罕见的先天性病变,据推测是由胚胎外胚层和内胚层组织之间异常的持续通信引起的。它们可能有症状,也可能无症状,通常具有潜伏和延长的临床病程。它们通常位于硬膜内和髓外。文献中很少报道髓外肠源性囊肿的病例,大多数是颅内囊肿。我们报告一个罕见的病例,位于胸椎水平的硬膜外肠源性囊肿,在放射学评估上模仿孤立的胸前脑膜膨出。病例报告:一个4岁的男孩被转介到我们的脊柱外科评估和处理偶然发现的T1椎体异常。磁共振成像显示T1椎体右半部分存在局灶性缺损,可见一个充满液体的囊通过该缺损突出到椎前和右侧椎旁区域。诊断为胸前脑膜膨出,建议手术治疗。手术暴露囊的整个范围后,进行针吸减压病变,产生乳白色的粘性液体,与脑脊液不同。怀疑可能是肠源性囊肿。在椎弓根基部切除病变,并用小轮廓钢板闭合椎体缺损。组织病理学检查证实为肠源性囊肿。结论:胸椎前路脑膜膨出和脊柱肠源性囊肿在影像学上难以区分,只有通过组织病理学检查才能做出明确的诊断。在脑膜膨出的鉴别诊断中必须考虑肠源性囊肿的可能性,反之亦然。
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