Kubota Toshihiko, Sato Kazufumi, Takeuchi Hiroaki, Handa Yuji
Department of Neurosurgery, Faculty of Medical Sciences, Fukui University, Matsuoka, Fukui, Japan.
J Neurooncol. 2004 Jun;68(2):177-83. doi: 10.1023/b:neon.0000027760.84461.c7.
Intracranial epithelioid hemangioendothelioma (E-HE) is an extremely rare, vasoformative tumor with variable biological behavior. A huge E-HE confined to the upper side of the tentorium has not been documented previously. Recognizing E-HE as a specific vascular tumor is important, and complete tumor removal guarantees long-term survival. Here, we report an intracranial E-HE of a 24-year-old woman with the initial symptoms of progressive headache over several years. Magnetic resonance imaging revealed a huge tumor attached to the upper side of the right tentorium, with tentorial and tonsillar herniation, and secondary syringomyelia in the upper cervical spinal cord. The initial surgical attempt to remove the lesion was abandoned due to profuse bleeding from the tumor. One year after irradiation and 5 days after vascular embolization, the tumor could be removed totally. The final definitive diagnosis as E-HE was made by special immunohistochemical and electron microscopic study. The patient is free from the tumor 9 years after the second operation. Thus, E-HE is a highly vascular-rich tumor to excise, and we stress need for preoperative embolization and/or irradiation to remove huge tumor completely.
颅内上皮样血管内皮瘤(E-HE)是一种极为罕见的、具有多种生物学行为的血管形成性肿瘤。此前尚未有局限于小脑幕上侧的巨大E-HE的报道。认识到E-HE是一种特殊的血管肿瘤很重要,完整切除肿瘤可确保长期生存。在此,我们报告一名24岁女性的颅内E-HE,其最初症状为数年的进行性头痛。磁共振成像显示一个巨大肿瘤附着于右侧小脑幕上侧,伴有小脑幕和扁桃体疝,以及上颈髓继发性脊髓空洞症。由于肿瘤大量出血,最初切除病变的手术尝试被放弃。放疗一年后及血管栓塞5天后,肿瘤得以完全切除。通过特殊免疫组化和电子显微镜研究最终确诊为E-HE。二次手术后9年,患者未再出现肿瘤。因此,E-HE是一种血管极为丰富的肿瘤,难以切除,我们强调术前栓塞和/或放疗对于完全切除巨大肿瘤的必要性。