Long-term follow up of malignant transformation of epidermoid cyst at the cerebellopontine angle based on serial imaging findings; A case report and literature review.

IF 0.4 Q4 ONCOLOGY
International Cancer Conference Journal Pub Date : 2026-03-03 eCollection Date: 2026-04-01 DOI:10.1007/s13691-026-00853-7
Koji Saito, Akihiko Teshigawara, Miku Maeda, Nei Fukasawa, Yasuharu Akasaki, Yuzuru Hasegawa, Masayuki Shimoda, Yuichi Murayama, Toshihide Tanaka
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引用次数: 0

Abstract

We report a case of malignant transformation of epidermoid cysts during long-term follow up more than 10 years with literature review. Epidermoid cysts are benign congenital tumors, accounting for 0.2-1.8% of intracranial tumors. Malignant transformation is extremely rare, with limited reports describing the imaging features and prognosis. A 69-year-old woman had presented with a tumor exhibiting hyperintensity on diffusion-weighted imaging at the left cerebellopontine angle and had been followed-up for the past decade. After 10 years, she developed left facial paralysis and hearing impairment. Contrast-enhanced lesions appeared within the tumor, accompanied by edema. Intraoperative findings revealed a tumor with two distinct components of pearly tumor and hematoma invading the cranial nerves. The pathological diagnosis was squamous cell carcinoma without primary malignancies, suggesting malignant transformation of epidermoid cyst. Although the residual tumor initially seemed dormant after postoperative radiotherapy, the patient developed carcinomatous meningitis. The literature was searched for squamous cell carcinoma without primary cancers showing neuroradiological changes in signal intensity on diffusion- and T2-weighted imaging, revealing 103 cases with a mean interval of 106.1 months from initial diagnosis to malignant transformation of epidermoid cyst. Although postoperative radiotherapy or chemotherapy has been attempted, no standard has been established for adjuvant treatment. The clinical benefits of postoperative adjuvant therapy need to be confirmed in further studies. As neuroradiological alterations on diffusion-weighted imaging or Gd-enhanced T1-weighted imaging during follow-up of epidermoid cyst might indicate malignant transformation of epidermoid cyst, postoperative radiotherapy might be an option worth exploring.

基于系列影像学表现的桥小脑角表皮样囊肿恶性转化的长期随访病例报告及文献复习。
我们报告一例表皮样囊肿恶性转化的长期随访超过10年,并复习文献。表皮样囊肿是先天性良性肿瘤,占颅内肿瘤的0.2-1.8%。恶性转化极为罕见,有关其影像学特征和预后的报道有限。一位69岁的女性,在左侧桥小脑角的弥散加权成像上表现为高强度的肿瘤,并在过去的十年中进行了随访。10年后,她患上了左侧面瘫和听力障碍。肿瘤内出现对比增强病变,伴水肿。术中发现一种具有珍珠状肿瘤和侵犯脑神经的血肿两种不同成分的肿瘤。病理诊断为无原发恶性的鳞状细胞癌,提示为表皮样囊肿的恶性转化。虽然术后放疗后残留肿瘤最初似乎处于休眠状态,但患者发展为癌性脑膜炎。我们检索了无原发癌的鳞状细胞癌,在弥散和t2加权成像上表现出信号强度的神经影像学改变,共发现103例,从初诊到表皮样囊肿恶性转化平均间隔106.1个月。术后虽尝试过放疗或化疗,但辅助治疗尚无标准。术后辅助治疗的临床疗效有待进一步研究证实。由于表皮样囊肿随访时弥散加权成像或gd增强t1加权成像的神经影像学改变可能提示表皮样囊肿恶性转化,因此术后放疗可能是一种值得探索的选择。
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来源期刊
自引率
14.30%
发文量
57
期刊介绍: This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO). - Presents an online-only collection of original case reports on all types of cancer - In particular, welcomes molecularly analyzed cancer cases - The Official Publication of the Japan Society of Clinical Oncology (JSCO)
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