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儿童颅内畸胎瘤:一项临床病理研究

Intracranial teratomas in children: a clinicopathological study.

作者信息

Goyal Nishant, Kakkar Aanchal, Singh Pankaj Kumar, Sharma Mehar Chand, Chandra Poodipedi Sarat, Mahapatra Ashok Kumar, Sharma Bhawani Shankar

机构信息

Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, 110029, India,

出版信息

Childs Nerv Syst. 2013 Nov;29(11):2035-42. doi: 10.1007/s00381-013-2091-y. Epub 2013 Apr 9.

Abstract

INTRODUCTION

Intracranial teratoma is a rare entity, accounting for 0.5 % of all intracranial tumors and 2-4 % of intracranial tumors in children.

OBJECTIVE

To study the demographic profile, clinical, radiological, and histopathological features of pediatric intracranial teratomas.

METHODS

All cases of intracranial teratoma diagnosed over an 11-year period (2001-2011) were retrieved from records of the departments of Neurosurgery and Neuropathology. Patients' demographic profile, clinical and radiological features and intraoperative findings were recorded.

RESULTS

We identified 43 cases of CNS teratoma, which included 8 adults and 35 children. Of the pediatric cases, 23 were spinal in location. Twelve cases of pediatric intracranial teratoma were identified (eight males, four females). Eight occurred in the first decade and four in the second decade (age range 3 days to 16 years). Third ventricle was the most common site (six cases). Four cases were seen in association with occipital encephalocele. All patients underwent surgery except for a newborn, which died 3 days after birth and was autopsied. Histologically, eight cases were classified as mature teratomas and four as immature teratomas. All four cases of immature teratoma were located in the posterior third ventricle.

CONCLUSION

A diagnosis of teratoma should be considered in young children presenting with a solid-cystic tumor in the region of the posterior third ventricle. Teratomas located in the posterior third ventricle are more likely to have immature components. In view of the coexistence of teratoma with occipital encephalocele, thorough histopathological sampling of the excised sac and contents is advised.

摘要

引言

颅内畸胎瘤是一种罕见的疾病,占所有颅内肿瘤的0.5%,占儿童颅内肿瘤的2 - 4%。

目的

研究儿童颅内畸胎瘤的人口统计学特征、临床、放射学和组织病理学特征。

方法

从神经外科和神经病理学部门的记录中检索出在11年期间(2001 - 2011年)诊断的所有颅内畸胎瘤病例。记录患者的人口统计学特征、临床和放射学特征以及术中发现。

结果

我们确定了43例中枢神经系统畸胎瘤病例,其中包括8例成人和35例儿童。在儿童病例中,23例位于脊柱。确定了12例儿童颅内畸胎瘤(8例男性,4例女性)。8例发生在第一个十年,4例发生在第二个十年(年龄范围3天至16岁)。第三脑室是最常见的部位(6例)。4例与枕部脑膨出相关。除一名出生后3天死亡并进行尸检的新生儿外,所有患者均接受了手术。组织学上,8例被分类为成熟畸胎瘤,4例为未成熟畸胎瘤。所有4例未成熟畸胎瘤均位于第三脑室后部。

结论

对于在第三脑室后部区域出现实性 - 囊性肿瘤的幼儿,应考虑畸胎瘤的诊断。位于第三脑室后部的畸胎瘤更可能具有未成熟成分。鉴于畸胎瘤与枕部脑膨出并存,建议对切除的囊袋和内容物进行彻底的组织病理学取样。

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