Kiran Narayanam Anantha Sai, Suri Ashish, Kasliwal Manish Kumar, Garg Anil, Ahmad Faiz Uddin, Mahapatra Ashok Kumar
Department of Neurosurgery, Seventh floor, Cardio NeuroSciences Centre, All India Institute of Medical Sciences, New Delhi 110029, India.
Childs Nerv Syst. 2008 Mar;24(3):385-91. doi: 10.1007/s00381-007-0522-3. Epub 2007 Nov 23.
Craniopharyngiomas with a large posterior fossa extension beyond the level of the foramen magnum are very rare and usually removed in two stages. The objective of this paper is to report that such rare cases of giant cystic predominantly retrochiasmatic retroclival craniopharyngiomas can be completely excised by an anterior transpetrous approach in a single stage.
The first case was a 6-year-old boy who presented with a 1-year history of recurrent episodes of seizures, headache, and vomiting. The second case was a 10-year-old girl who presented with history of headache, visual deterioration, and left-side hemiparesis for one and half years. Preoperative computed tomography (CT) and magnetic resonance imaging (MRI) in both these patients revealed a giant sellar suprasellar cystic lesion with areas of calcification and the lesion was predominantly retrochiasmatic with a huge retroclival posterior fossa extension down to the level of the C1 vertebra and laterally to the cerebellopontine angle. Gross total excision of both suprasellar and posterior fossa extensions could be done in both the patients through an anterior transpetrous transtentorial approach (Kawase's approach).
Postoperative imaging (MRI/CT) revealed no obvious evidence of residual tumor. The first patient had right hemiparesis from which he recovered completely. The second patient died suddenly on postoperative day 4 after initial uneventful postoperative period, and the exact cause of death is not known.
Giant cystic craniopharyngiomas, which are predominantly retrochiasmatic and associated with huge retroclival posterior fossa extensions, can be removed in single stage by Kawase's approach.
后颅窝延伸至枕骨大孔水平以下的颅咽管瘤非常罕见,通常分两期切除。本文的目的是报告此类罕见的巨大囊性、主要位于视交叉后斜坡后颅窝的颅咽管瘤可通过经岩前入路一期完全切除。
第一例为一名6岁男孩,有1年癫痫发作、头痛和呕吐反复发作史。第二例为一名10岁女孩,有1年半头痛、视力减退和左侧偏瘫病史。这两名患者术前的计算机断层扫描(CT)和磁共振成像(MRI)均显示鞍上巨大囊性病变,伴有钙化区域,病变主要位于视交叉后,巨大的斜坡后颅窝延伸至C1椎体水平,外侧至桥小脑角。通过经岩前经小脑幕入路(Kawase入路),两名患者的鞍上和后颅窝延伸部分均实现了全切。
术后影像学检查(MRI/CT)显示无明显肿瘤残留迹象。第一例患者出现右侧偏瘫,但已完全康复。第二例患者在术后初期情况平稳后于术后第4天突然死亡,确切死因不明。
主要位于视交叉后且伴有巨大斜坡后颅窝延伸的巨大囊性颅咽管瘤可通过Kawase入路一期切除。