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垂体腺瘤放疗30年后发生的非典型小脑幕脑膜瘤。

Atypical tentorial meningioma 30 years after radiotherapy for a pituitary adenoma.

作者信息

Santoro A, Minniti G, Paolini S, Passacantilli E, Missori P, Frati A, Cantore G P

机构信息

Neurosurgery Unit I, Department of Neurological Sciences, La Sapienza University of Rome, Viale dell'Università 30a, Italy.

出版信息

Neurol Sci. 2002 Mar;22(6):463-7. doi: 10.1007/s100720200007.

Abstract

Although the human central nervous system used to be considered relatively resistant to the carcinogenic action of ionizing radiation, several lines of evidence now document a high incidence of secondary tumors in irradiated patients. The numerous reports of radiation-induced cerebral meningiomas generally distinguish those induced by high-dose radiation from those induced by low-dose radiation. We describe the case of patient who underwent subtotal resection of a chromophobe pituitary adenoma at the age of 18 years, who was successively treated by conventional fractionated radiotherapy with gamma rays emitted by a source of 60Co until a total dose of 41 Gy. Over the next 30 years the patient experienced all the known late effects of radiation, including panhypopituitarism, cranial-nerve deficits (II, III and VI), massive radiation necrosis involving the left cerebral hemisphere and causing right hemiparesis and aphasia and, ultimately, an atypical tentorial meningioma with early recurrence after total resection.

摘要

尽管人类中枢神经系统曾被认为对电离辐射的致癌作用具有相对抗性,但现在有几条证据表明,接受过辐射的患者继发肿瘤的发生率很高。关于辐射诱发的脑脑膜瘤的大量报告通常将高剂量辐射诱发的肿瘤与低剂量辐射诱发的肿瘤区分开来。我们描述了一名患者的病例,该患者18岁时接受了嫌色性垂体腺瘤的次全切除术,随后接受了60Co源发射的γ射线常规分割放疗,直至总剂量达到41Gy。在接下来的30年里,该患者经历了所有已知的辐射晚期效应,包括全垂体功能减退、颅神经缺损(II、III和VI)、累及左脑半球的大面积放射性坏死并导致右半身轻瘫和失语,最终患上了非典型小脑幕脑膜瘤,全切除术后早期复发。

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