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三例急性淋巴细胞白血病完全缓解后发生的放射性诱导胶质母细胞瘤病例报告。

Three case reports of radiation-induced glioblastoma after complete remission of acute lymphoblastic leukemia.

机构信息

Department of Neurosurgery, Graduate School of Medicine, Tohoku University, 1-1 Seiryo-cho, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Department of Pediatrics, Graduate School of Medicine, Tohoku University, Sendai, Miyagi, Japan.

出版信息

Brain Tumor Pathol. 2018 Apr;35(2):114-122. doi: 10.1007/s10014-018-0316-1. Epub 2018 Apr 17.

Abstract

Radiation therapy is sometimes performed to control intracranial acute lymphoblastic leukemia (ALL), but may lead to radiation-induced malignant glioma. The clinical, radiological, histological, and molecular findings are described of three cases of radiation-induced glioblastoma after the treatment for ALL. They received radiation therapy at age 6-8 years. The latency from radiation therapy to the onset of radiation-induced glioblastoma was 5-10 years. Magnetic resonance imaging demonstrated diffuse lesions with multiple small enhanced lesions in all cases. Histological examination showed that the tumors consisted of mainly small round astrocytic atypical cells in one case, and astrocytic atypical cells with elongated cytoplasm and nuclear pleomorphism with small cell component in two cases. Microvascular proliferation was present in all cases. Immunohistochemical analysis for B-Raf V600E, and mutational analysis for the isocitrate dehydrogenase (IDH) 1, IDH2, and H3F3A gene revealed the wild-type alleles in all three cases. The integrated diagnoses were IDH wild-type glioblastoma, and local irradiation and concomitant temozolomide were performed. After the initial treatment, significant shrinkage of the diffuse lesion and enhanced lesion was found in all cases. Radiation-induced glioblastoma occurring after the treatment for ALL had unique clinical, radiological, histological, and molecular characteristics in our three cases.

摘要

放射治疗有时用于控制颅内急性淋巴细胞白血病(ALL),但可能导致放射性诱导性恶性胶质瘤。我们描述了三例 ALL 治疗后发生放射性脑胶质瘤的临床、影像学、组织学和分子学特征。他们在 6-8 岁时接受放射治疗。从放射治疗到放射性脑胶质瘤发病的潜伏期为 5-10 年。磁共振成像显示所有病例均有弥漫性病变,伴有多个小增强病变。组织学检查显示,1 例肿瘤主要由小圆形星形细胞非典型细胞组成,2 例肿瘤由长形细胞质和核多形性的星形细胞非典型细胞与小细胞成分组成。所有病例均存在微血管增生。所有 3 例病例的 B-Raf V600E 免疫组化分析和异柠檬酸脱氢酶(IDH)1、IDH2 和 H3F3A 基因突变分析均显示野生型等位基因。综合诊断为 IDH 野生型脑胶质瘤,并进行局部放疗和同时替莫唑胺治疗。在初始治疗后,所有病例弥漫性病变和增强病变均明显缩小。我们的三例病例显示,ALL 治疗后发生的放射性脑胶质瘤具有独特的临床、影像学、组织学和分子学特征。

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