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中颅窝区域的异位神经胶质神经元组织。四例报告。

Ectopic glioneuronal tissue in the middle cranial fossa region. Report of four cases.

作者信息

Abel Taylor J, Chowdhary Abhineet, Thapa Mahesh, Rutledge Joseph C, Gruss Joseph, Manning Scott, Avellino Anthony M

机构信息

Departments of Neurological Surgery, University of Washington chool of Medicine, Seattle, Washington 98105, USA. .

出版信息

J Neurosurg Pediatr. 2009 Mar;3(3):188-96. doi: 10.3171/2008.12.PEDS0892.

Abstract

The growth of ectopic glioneuronal tissue in the middle cranial fossa region is an uncommon event, with very few cases reported in the literature. In this paper the authors document 4 cases of ectopic glioneuronal tissue in the middle cranial fossa in children and briefly describe the clinical course and pathology. All of the children presented within the first 6 months of life. Two children presented with facial masses, 1 with airway obstruction, and another with proptosis of the right eye. Each child underwent a customized surgery dependent on the location and characteristics of the harbored lesion. Ectopic glioneuronal masses in the middle cranial fossa are rare and benign congenital tumors, and affected newborns can present with airway obstruction, feeding difficulties, and facial deformity depending on the lesion location. Determining an appropriate surgical approach and strategy is a significant challenge and may involve a multidisciplinary team of craniofacial plastic surgeons, otolaryngologists, and neurosurgeons. Although these lesions share clinical and anatomical similarities, because of their histopathological heterogeneity, it is unlikely that they represent a single pathological entity. The long-term outcome in these children is still unknown and is an area for future study. The pathogenesis of these lesions also remains unknown and may be revealed in future research.

摘要

中颅窝区域异位神经胶质神经元组织的生长是一种罕见事件,文献中报道的病例极少。在本文中,作者记录了4例儿童中颅窝异位神经胶质神经元组织病例,并简要描述了临床病程和病理情况。所有患儿均在出生后的前6个月内就诊。2例患儿表现为面部肿块,1例出现气道梗阻,另1例右眼突出。每个患儿都根据所患病变的位置和特征接受了定制手术。中颅窝异位神经胶质神经元肿块是罕见的良性先天性肿瘤,根据病变位置,受影响的新生儿可能会出现气道梗阻、喂养困难和面部畸形。确定合适的手术方法和策略是一项重大挑战,可能需要颅面整形外科医生、耳鼻喉科医生和神经外科医生组成的多学科团队参与。尽管这些病变在临床和解剖学上有相似之处,但由于其组织病理学的异质性,它们不太可能代表单一的病理实体。这些患儿的长期预后仍然未知,是未来研究的一个领域。这些病变的发病机制也仍然未知,可能会在未来的研究中揭示。

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