Dokumcu Zafer, Uygun Ozgun, Turhan Tuncer, Yalaz Mehmet, Ozcan Coskun, Erdener Ata
Department of Pediatric Surgery, Division of Pediatric Thoracic Surgery, Ege University Faculty of Medicine, Izmir, Turkey,
Childs Nerv Syst. 2015 Feb;31(2):185-9. doi: 10.1007/s00381-014-2553-x. Epub 2014 Sep 19.
Neuroenteric cysts (NC) are rare pathologies and localized generally in posterior mediastinum or abdomen where they may extend to spinal canal through a vertebral defect. Isolated spinal lesions require dorsal/ventral laminectomy and thoracic ones thoracotomy or thoracoscopy. Posterolateral approach via thoracotomy is generally performed for lesions with both thoracic and spinal components. Minimal invasive excision of a thoracic NC with spinal extension in an infant is presented herein.
A term female newborn with an antenatal (26th week) diagnosis of congenital diaphragmatic hernia (CDH) was admitted. On physical examination, she was normal except mild dyspnea and CDH were excluded on radiogram. Left parenchymal opacity necessitated thorax tomography that revealed lobulated cystic lesion (6 × 3.5 × 4.5 cm) in posterior mediastinum. MRI showed intraspinal extension of the lesion through a hemivertebrae (6th). Two-stage procedure was planned for suspected neuroenteric cyst. First, intraspinal component was excised with dorsal laminectomy and the connection was closed. Then, the thoracic component was excised thoracoscopically. Histopathological evaluation confirmed the diagnosis. Total parenteral nutrition and high dose somatostatin analog was needed due to transient left chylothorax on postoperative course. She was well and symptom-free in postoperative period.
Neuroenteric cysts may lead to misdiagnoses in antenatal period. MRI is critical to show spinal and vertebral pathologies in suspected cases. Thoracoscopy may safely be performed for thoracic lesions with spinal extension in two-stage approach following closure of the connection and excision of the spinal component.
神经肠囊肿(NC)是一种罕见的病变,通常位于后纵隔或腹部,可通过椎体缺损延伸至椎管。孤立的脊柱病变需要进行背侧/腹侧椎板切除术,而胸部病变则需要开胸手术或胸腔镜手术。对于同时累及胸部和脊柱的病变,通常采用经胸后外侧入路。本文介绍了一名婴儿胸段神经肠囊肿伴脊柱延伸的微创切除术。
一名足月女婴因产前(第26周)诊断为先天性膈疝(CDH)入院。体格检查时,除轻度呼吸困难外,她一切正常,X线检查排除了CDH。左肺实质模糊影需要进行胸部断层扫描,结果显示后纵隔有分叶状囊性病变(6×3.5×4.5厘米)。MRI显示病变通过半椎体(第6个)向椎管内延伸。对于疑似神经肠囊肿,计划采用两阶段手术。首先,通过背侧椎板切除术切除椎管内部分,并封闭连接部。然后,通过胸腔镜切除胸部部分。组织病理学评估证实了诊断。术后因短暂性左乳糜胸,需要全胃肠外营养和高剂量生长抑素类似物治疗。术后她情况良好,无任何症状。
神经肠囊肿在产前可能导致误诊。MRI对于疑似病例显示脊柱和椎体病变至关重要。对于伴有脊柱延伸的胸部病变,在封闭连接部并切除椎管内部分后,可采用两阶段方法安全地进行胸腔镜手术。