头皮鳞状细胞癌放疗后放疗诱发的低级别胶质瘤:病例报告和文献综述。

IF 0.6 Q4 SURGERY Case Reports in Surgery Pub Date : 2024-07-09 eCollection Date: 2024-01-01 DOI:10.1155/2024/1907435
Moayad M Z Ahmed, Fawaz E M Abdelradi, Rabee A ELfeel
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引用次数: 0

摘要

前言放射诱导胶质瘤(RIGs)在文献中多有报道。在大多数报道的病例和综述文章中,患者都有原发性颅内肿瘤病史,如颅咽管瘤、髓母细胞瘤和上皮瘤,常见的继发性肿瘤是脑膜瘤和肉瘤,主要不是胶质瘤。病例介绍。一名 50 岁的女性曾患左侧头皮颞区耳周鳞状细胞癌,11 年前的活组织检查结果证实了这一点。在此基础上,她在 39 岁时开始接受低剂量放射治疗。9 年后,她出现了头颅症状和癌症放射学征兆。切除手术成功后,组织学显示为弥漫性星形细胞瘤 2 级。我们的病例被怀疑符合 RIG 的鉴定标准,而这种综合征在文献中并不常见:总之,由于患者年龄较大,接受的辐射剂量较低,我们病例中的表现方式被认为是罕见的。尽管基因研究是确诊的重要依据,但遗憾的是,我们并没有对我们的病例进行基因研究,而是主要依据 Cahan 等人提到的标准,这些标准主要来自临床病史和组织病理学。在此,我们举例说明,如果临床上怀疑有这种诊断,即使当地没有遗传学研究,也应考虑进行遗传学研究以确诊。
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Radiation-Induced Low-Grade Glioma following Radiotherapy for Squamous Cell Carcinoma of the Scalp: Case Report and Literature Review.

Introduction: Radiation-induced gliomas (RIGs) were reported in the literature in general. In most of the reported cases and the reviewed articles, patients have a history of primary intracranial tumors like craniopharyngioma, medulloblastoma, and ependymoma, and the commonly resulting secondary tumors are meningiomas and sarcomas, mainly not gliomas. Case Presentation. A 50-year-old woman had a history of left scalp temporal region periauricular squamous cell carcinoma, which was verified by the histology result of a biopsy 11 years ago. On the basis of that, she began receiving low-dose radiation sessions when she was 39 years old. She exhibits cranial symptoms and a radiological sign of cancer 9 years later. After a successful excision procedure, histology revealed diffuse astrocytoma Grade 2. Our case is suspected to fit the criteria for being identified as RIG, which is a syndrome that is thought to occur infrequently in the literature.

Conclusion: In conclusion, the way that this condition manifested in our case is considered rare due to old age and the low doses of radiation received. Despite being an important part to confirm the diagnosis, genetic studies were unfortunately not done in our case, but we mainly based on the criteria mentioned by Cahan et al., which are mainly taken from the clinical history and histopathology. Here, we present an example of considering such a diagnosis when suspected clinically, but a genetic study for confirmation should be thought of even if it is not available in the locality.

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