Papillary Tumor of the Pineal Region Treated With Surgery and Postoperative Radiotherapy: A Case Report.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2025-01-25 eCollection Date: 2025-01-01 DOI:10.7759/cureus.77989
Benjamin Royal-Preyra, Melanie Boucher
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Abstract

Papillary tumors of the pineal region (PTPR) are extremely rare malignancies that make up less than 0.1% of primary brain tumors. They are usually treated with surgery and adjuvant tumor bed radiotherapy (RT). We review the case of a man in his late 60s who presented with two weeks of confusion and ataxia. Imaging the head with computed tomography (CT) and magnetic resonance imaging (MRI) showed hydrocephalus and a 2 cm pineal region mass. We review the presenting symptoms, investigations, and differential diagnosis for patients with pineal region masses. The pathological features, initial hydrocephalus management, and curative treatment of his tumor with surgery and RT are discussed. We also review the PTPR literature, including prognostic features and the evidence for treatment modalities, and report adjuvant radiotherapy treatment planning volumes. The patient is symptom-free and without evidence of recurrent disease on follow-up MRI 18 months after treatment. PTPR has very high recurrence rates following treatment; less than 20% of patients have local control at 10 years, and further research is needed to find more effective interventions and improve patient outcomes.

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用手术和术后放疗治疗松果体乳头状肿瘤:病例报告
松果体区乳头状肿瘤(PTPR)是一种极为罕见的恶性肿瘤,占原发性脑肿瘤的不到0.1%。它们通常通过手术和辅助肿瘤床放疗(RT)治疗。我们回顾了一个60多岁的男人,他表现出两周的精神错乱和共济失调。头部计算机断层扫描(CT)和磁共振成像(MRI)显示脑积水和2厘米的松果体区肿块。我们回顾了松果体区肿块患者的表现、检查和鉴别诊断。我们讨论了他的病理特点,初次脑积水的处理,以及手术和放射治疗的疗效。我们还回顾了PTPR的文献,包括预后特征和治疗方式的证据,并报告了辅助放疗治疗计划量。患者无症状,治疗后18个月复查MRI无疾病复发迹象。PTPR治疗后复发率非常高;不到20%的患者在10年内获得局部控制,需要进一步研究以找到更有效的干预措施并改善患者预后。
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