Weng Jian-Cong, Ma Jun-Peng, Hao Shu-Yu, Wang Liang, Xu Yu-Lun, Yang Jun, Jia Wen-Qing, Wu Zhen, Zhang Li-Wei, Li Da, Zhang Jun-Ting
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing; China National Clinical Research Center for Neurological Diseases, Beijing; Center of Brain Tumor, Beijing Institute for Brain Disorders, Beijing; and Beijing Key Laboratory of Brian Tumor, Beijing, People's Republic of China.
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing; China National Clinical Research Center for Neurological Diseases, Beijing; Center of Brain Tumor, Beijing Institute for Brain Disorders, Beijing; and Beijing Key Laboratory of Brian Tumor, Beijing, People's Republic of China.
World Neurosurg. 2018 Jan;109:e571-e580. doi: 10.1016/j.wneu.2017.10.023. Epub 2017 Nov 14.
An intradural extramedullary bronchogenic cyst (IEBC) is a congenital malformation and an extremely rare type of endodermal cyst. This study aims to report the clinical and radiologic characteristics and surgical outcomes of IEBCs and to review the available literature.
The medical records of 6 patients (3 female) with pathologically confirmed bronchogenic cysts involving the spinal cord between 2009 and 2016 were retrospectively reviewed, and follow-up evaluations were performed.
Of the 6 symptomatic lesions, 4 were located in the cervical vertebra, 1 at the lumbar vertebra, and the remaining 1 at the craniocervical junction. Radiographs showed signals similar to cerebral spinal fluid on all magnetic resonance imaging sequences without contrast enhancement. Total resection was achieved in 3 patients. Histopathology revealed simple and pseudostratified respiratory epithelium with benign subepithelial mucous glands and fat components neighboring the cyst. After a mean follow-up duration of 49.2 months, 2 asymptomatic residual lesions regrew after nontotal resection. In previous literature including 19 cases, most IEBCs (84.2%) tended to be homogeneous and well demarcated on radiologic images, and 85.7% were not contrast enhancing. Cervical or upper thoracic segments were predilection sites with intradural extramedullary localization. The majority of IEBCs had similar benign histological features. The recurrence rate was 15.4% after nontotal resection but nil after total resection.
IEBCs displayed an indolent course, and the most effective management with positive outcomes was total resection. Nontotal resection, cystic fenestration, and biopsy, which were associated with recurrence, should be avoided.
硬脊膜内髓外支气管源性囊肿(IEBC)是一种先天性畸形,是极为罕见的内胚层囊肿类型。本研究旨在报告IEBC的临床和影像学特征及手术结果,并对现有文献进行综述。
回顾性分析2009年至2016年间6例经病理证实累及脊髓的支气管源性囊肿患者(3例女性)的病历,并进行随访评估。
6个有症状的病灶中,4个位于颈椎,1个位于腰椎,其余1个位于颅颈交界处。所有磁共振成像序列上的X线片显示信号与脑脊液相似,无对比增强。3例患者实现了全切除。组织病理学显示为单层和假复层呼吸上皮,囊肿周围有良性上皮下黏液腺和脂肪成分。平均随访49.2个月后,2例无症状残留病灶在未全切除后复发。在包括19例病例的既往文献中,大多数IEBC在影像学上倾向于均匀且边界清晰,85.7%无对比增强。颈椎或上胸段是硬脊膜内髓外定位的好发部位。大多数IEBC具有相似的良性组织学特征。未全切除后的复发率为15.4%,全切除后无复发。
IEBC病程进展缓慢,最有效的治疗方法且预后良好的是全切除。应避免未全切除、囊肿开窗和活检,因为这些操作与复发相关。