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[中枢神经系统原始神经外胚层肿瘤疑似髓母细胞瘤放疗后二次复发:一例报告]

[CNS primitive neuroectodermal tumor suspected as a secondary recurrence after radiation therapy for medulloblastoma:a case report].

作者信息

Sato Hiroyuki, Shibuya Kouhei, Koizumi Takayuki, Kato Shunichi, Endo Shin

机构信息

Department of Neurosurgery, Takeda General Hospital.

出版信息

No Shinkei Geka. 2014 Jul;42(7):641-50.

Abstract

We report a case of a suspected secondary central nervous system(CNS)primitive neuroectodermal tumor(PNET)that developed 25 years after radiation therapy for a medulloblastoma of the cerebellum. At 5 years of age, the patient underwent craniotomy and subsequent radiation therapy of the whole brain(39Gy), whole spinal cord(9Gy), and posterior fossa(49Gy)for the treatment of a medulloblastoma of the cerebellum;the patient did not receive chemotherapy. After radiation therapy, the medulloblastoma completely receded and did not recur. Twenty-five years later, at 30 years of age, the patient visited our institution experiencing right-sided hemiparesis and aphasia that had arisen approximately 1 month prior and had gradually worsened. The patient was subsequently hospitalized after experiencing disturbed consciousness and a generalized convulsion seizure. Gadolinium-enhanced magnetic resonance imaging(MRI)revealed a mass accompanied by a large cyst in the left frontal lobe. Complete tumor resection was achieved via macroscopic surgery, and the histopathological findings were indicative of CNS PNET. Considering the tumor occurred in the same site where radiation therapy had been previously administered to treat a medulloblastoma, additional radiotherapy was avoided in favor of combination chemotherapy with ifosfamide, cisplatin, and etoposide. Tumor recurrence was not observed in a follow-up MRI after 6 courses of ICE therapy, and the patient has resumed a normal life. The present case, a CNS PNET, is suspected as a secondary brain tumor induced by radiation therapy previously used to treat a medulloblastoma, and it represents a rare late-onset complication of radiation therapy. For the treatment of PNET, we believe that maximal safe surgical resection of the tumor and post-operative radiation therapy are typically necessary for long-term survival. However, taking into account the risks of repeated exposure to radiation, we did not perform post-operative radiation therapy for this patient. We have not observed recurrence to date;however, the patient will require a strict follow-up schedule hereafter.

摘要

我们报告一例疑似继发性中枢神经系统(CNS)原始神经外胚层肿瘤(PNET),该肿瘤在小脑髓母细胞瘤放射治疗25年后发生。患者5岁时因小脑髓母细胞瘤接受了开颅手术及随后的全脑放射治疗(39Gy)、全脊髓放射治疗(9Gy)和后颅窝放射治疗(49Gy);患者未接受化疗。放射治疗后,髓母细胞瘤完全消退且未复发。25年后,患者30岁时因约1个月前出现的右侧偏瘫和失语前来我院就诊,症状逐渐加重。患者随后在出现意识障碍和全身性惊厥发作后住院。钆增强磁共振成像(MRI)显示左额叶有一个伴有大囊肿的肿块。通过宏观手术实现了肿瘤的完全切除,组织病理学检查结果提示为CNS PNET。考虑到肿瘤发生在先前因髓母细胞瘤接受放射治疗的同一部位,避免了额外的放射治疗,转而采用异环磷酰胺、顺铂和依托泊苷联合化疗。在接受6个疗程的ICE治疗后的随访MRI中未观察到肿瘤复发,患者已恢复正常生活。本病例为CNS PNET,疑似为先前用于治疗髓母细胞瘤的放射治疗诱发的继发性脑肿瘤,它代表了一种罕见的放射治疗晚期并发症。对于PNET的治疗,我们认为为实现长期生存,通常需要对肿瘤进行最大程度的安全手术切除及术后放射治疗。然而,考虑到重复接受放射治疗的风险,我们未对该患者进行术后放射治疗。迄今为止我们未观察到复发;然而,该患者此后需要严格的随访计划。

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