A New Sarcoma Shortly after Treatment for High-Grade Glioma with Adjuvant Chemoradiation: A Case Report

被引:1
作者
Madkhali, Abdossalam M. [1 ]
Alaluan, Hasah F. [2 ]
Alnajeim, Mohammed H. [2 ]
Al Saeed, Eyad F. [1 ]
Ajlan, Abdulrazag M. [3 ]
Abdelwarith, Ahmed [4 ]
Abduh, Ali [5 ]
Albanyan, Saleh [6 ,7 ]
Alqurashi, Ashwag [8 ]
Alkhalidi, Hisham [9 ]
机构
[1] King Saud Univ, Coll Med, Oncol Hematol & Radiat Oncol Unit, Dept Med, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Med, Riyadh, Saudi Arabia
[3] King Saud Univ, Surg Dept, Coll Med, Riyadh, Saudi Arabia
[4] King Saud Univ, Oncol Ctr, Riyadh, Saudi Arabia
[5] King Saud Univ, King Khalid Univ Hosp, King Saud Univ Med City, Dept Radiol, Riyadh, Saudi Arabia
[6] King Saud Univ, Coll Med, Dept Internal Med, Riyadh, Saudi Arabia
[7] King Saud Univ, King Khalid Univ Hosp, King Saud Univ Med City, Riyadh, Saudi Arabia
[8] King Saud Univ Med City, Dept Surg, Div Neurosurg, Riyadh, Saudi Arabia
[9] King Saud Univ, Coll Med, Dept Pathol, Riyadh, Saudi Arabia
来源
CASE REPORTS IN ONCOLOGY | 2024年 / 17卷 / 01期
关键词
Sarcoma; High-grade glioma; Glioblastoma; Radiation; Complication; Secondary cancer; RADIATION-INDUCED SARCOMA; GUIDELINES;
D O I
10.1159/000538508
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: High-grade gliomas are central nervous system tumors conventionally treated with surgery followed by adjuvant chemoradiotherapy. Secondary cancer due to radiation therapy is a rare yet established phenomenon that typically occurs years after radiation therapy. Case Presentation: In this case, we discuss an early presentation of a second cancer adjacent to the radiation field. This case report is of a 52-year-old male who developed a new scalp sarcoma at the site of primary surgery 8 months after radiation therapy. Genetic testing revealed a heterozygous missense variant in the NF1 gene, a variant of uncertain significance. The report highlights that this case does not conform to the expected criteria for postradiation sarcoma in terms of timing. Conclusion: Secondary cancers may arise earlier than expected, even in phenotypically normal patients, as they may have unmanifested variants of relevant mutations. The question of pre-radiotherapy screening for radiosensitivity syndromes and diseases requires further study, as current data are limited and do not provide enough insight into the significance of different genetic variants. (c) 2024 The Author(s). Published by S. Karger AG, Basel
引用
收藏
页码:573 / 580
页数:8
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