Department of Surgical Oncology, Tata Memorial Centre, Parel, Mumbai, India.
Acta Neurochir (Wien). 2010 Jan;152(1):137-42. doi: 10.1007/s00701-009-0332-3. Epub 2009 Apr 30.
Residual radiologically progressive masses following multimodality treatment of malignant mixed intracranial germ cell tumors are described. Often these enlarge, and this is called the growing teratoma syndrome. A similar phenomenon during radiotherapy alone has not been described.
A 5-year old boy presented with features of raised intracranial pressure. Imaging revealed a posterior third ventricular mass, which was biopsied endoscopically.
A review of the scanty tissue was suggestive of a pineal parenchymal tumor, and hence radiation was planned. After just ten fractions, he developed rapid neurological deterioration. Repeat imaging raised a possibility of a teratomatous tumor. He underwent emergency excision. However, he had a stormy postoperative course and succumbed to deep venous infarction. Histology revealed a purely mature teratoma.
Though a growing teratoma syndrome has been described following chemotherapy, no such report while on radiation exists. Ours could be the first such reported case. We discuss the possible mechanisms with a review of the literature.
多模态治疗恶性混合性颅内生殖细胞肿瘤后残留的影像学进展性肿块被描述。这些肿块通常会增大,这被称为“生长性畸胎瘤综合征”。然而,单独放疗期间尚未描述过类似的现象。
一名 5 岁男孩因颅内压升高的症状就诊。影像学检查显示第三脑室后部有肿块,通过内镜进行了活检。
对少量组织的检查提示为松果体实质肿瘤,因此计划进行放疗。仅进行了 10 个疗程后,他的神经功能迅速恶化。重复的影像学检查提示存在畸胎瘤的可能性。他接受了紧急切除术。然而,他术后经历了严重的并发症,最终死于深静脉血栓形成。组织学检查显示为单纯成熟的畸胎瘤。
尽管已经描述了化疗后出现的“生长性畸胎瘤综合征”,但在放疗期间尚未有此类报告。我们报告的这个病例可能是首例。我们通过文献回顾讨论了可能的机制。