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弥漫性内生桥脑胶质瘤放疗后肿瘤消退显著:病例研究。

Exceptional Tumor Regression in Diffuse Intrinsic Pontine Glioma Post-Radiotherapy: A Case Study.

机构信息

Department of Radiotherapy, Datta Meghe Institute of Higher Education & Research, Sawangi, Wardha, India.

Department of Radiodiagnosis, Datta Meghe Institute of Higher Education & Research, Sawangi, Wardha, India.

出版信息

Am J Case Rep. 2024 Sep 30;25:e944869. doi: 10.12659/AJCR.944869.

Abstract

BACKGROUND Diffuse intrinsic pontine glioma represent approximately 10% to 20% of all pediatric central nervous system tumors. Classic brain stem symptoms are cranial nerve deficits, long tract signs, ataxia, alone or in combination. Focal radiotherapy has been the standard of care in patients with diffuse intrinsic pontine gliomas with minimum response. Here, we present an unusual case with excellent tumor regression with radiotherapy and good clinical outcome. CASE REPORT A 13-year-old girl presented with headache and imbalance during walking for the past 2-3 months, along with a deviation of the right eye in the last month. Brain magnetic resonance imaging (MRI) suggested a well-defined solid cystic altered-signal-intensity lesion involving the pons and medulla, causing its expansion up to the midbrain on the left side. The lesion was 4.6×3.7×3.6 cm. We applied the intensity-modulated radiotherapy technique (IMRT) using a 6-MV photon beam with the conventional dose fractionation of 54 Gy in 30 fractions (1.8 Gy/fraction). Three months later, MRI brain with spectroscopy and perfusion showed evidence of non-enhancing, altered-signal-intensity lesion in the pons and medulla, measuring 1.9×2.2×2.4 cm. CONCLUSIONS Early detection of symptoms of DIPG in a young patient along with effective radiological investigation with valid tumor board decision as definitive radiotherapy as a sole therapeutic treatment option and with robust radiotherapy planning resulted in an excellent response, with 80% reduction in gross tumor volume (GTV) as seen in pre-radiotherapy (RT) and post-RT MRI images.

摘要

背景

弥漫性内在脑桥神经胶质瘤占所有儿童中枢神经系统肿瘤的 10%至 20%左右。经典脑干症状是颅神经缺陷、长束征、共济失调,单独或组合出现。对于弥漫性内在脑桥神经胶质瘤患者,局限性放疗是标准治疗方法,其反应最小。在这里,我们报告了一个不寻常的病例,放疗后肿瘤有很好的消退,临床结果良好。

病例报告

一名 13 岁女孩因过去 2-3 个月头痛和行走时失去平衡,以及上个月右眼偏斜而就诊。脑部磁共振成像(MRI)提示累及脑桥和延髓的界限清楚的实性囊性信号改变的病变,导致其左侧扩展至中脑。病变大小为 4.6×3.7×3.6 厘米。我们应用强度调制放疗技术(IMRT),使用 6MV 光子束,常规剂量分割为 54Gy,共 30 次(1.8Gy/次)。三个月后,脑部 MRI 联合波谱和灌注显示脑桥和延髓内无强化、信号改变的病变,大小为 1.9×2.2×2.4 厘米。

结论

年轻患者出现 DIPG 症状时及早发现,结合有效的影像学检查和有效的肿瘤委员会决策,作为唯一的治疗选择,进行明确的放疗,并进行强有力的放疗计划,可获得极好的反应,与放疗前(RT)和放疗后 MRI 图像相比,肿瘤总体积(GTV)减少 80%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c5/11452143/2f9a32a5bd4f/amjcaserep-25-e944869-g001.jpg

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