Department of Neurological Surgery, Neurological Institute of New Jersey, UMDNJ-New Jersey Medical School, 90 Bergen Street Suite 8100, Newark, NJ 07101, USA.
J Neurooncol. 2012 Apr;107(2):427-34. doi: 10.1007/s11060-011-0764-5. Epub 2011 Nov 16.
Papillary tumor of the pineal region (PTPR) is a rare neuroepithelial tumor that arises in the pineal region. The optimal treatment for PTPR remains controversial, as no definitive treatment strategy exists for this lesion. It is not clear whether aggressive surgical removal is superior to biopsy followed by radiotherapy. The majority of cases in the literature have undergone attempted gross total resection with a supracerebellar-infratentorial or a transcallosal-transventricular approach. In this report, we describe a case of PTPR in a 23 year-old male that presented as a third ventricular mass causing obstructive hydrocephalus. An endoscopic third ventriculostomy was performed followed by an endoscopic biopsy. Postoperative radiotherapy resulted in complete regression of the tumor with no evidence of tumor recurrence at 25 months. This case highlights a minimally invasive strategy for a rare neoplasm that resulted in a favorable response to radiation therapy, thereby avoiding the risks of aggressive surgical removal. We also review the radiographic and histopathologic features of PTPR and discuss various options of treatment reported in the literature.
松果体区乳头状肿瘤(PTPR)是一种罕见的神经上皮肿瘤,发生于松果体区。对于 PTPR 的最佳治疗方法仍存在争议,因为对于这种病变没有明确的治疗策略。目前尚不清楚积极的手术切除是否优于活检后放疗。文献中的大多数病例都采用了经小脑幕上-小脑幕下或经胼胝体-透明隔-脑室入路进行了尝试性的大体全切除。在本报告中,我们描述了一例 23 岁男性患者,其表现为第三脑室肿块导致梗阻性脑积水。我们进行了内镜第三脑室造瘘术,随后进行了内镜活检。术后放疗导致肿瘤完全消退,25 个月时无肿瘤复发的证据。该病例强调了一种针对罕见肿瘤的微创策略,这种策略对放疗有良好的反应,从而避免了积极手术切除的风险。我们还回顾了 PTPR 的影像学和组织病理学特征,并讨论了文献中报道的各种治疗选择。