White epidermoid cyst transformation after stereotactic radiosurgery: illustrative case.

Hideki Matsumoto, Yuki Shinya, Satoru Miyawaki, Masahiro Shin, Satoshi Koizumi, Daisuke Sato, Munetoshi Hinata, Masako Ikemura, Satoshi Kiyofuji, Taich Kin, Mototaro Iwanaga, Masahiro Shimizu, Hirofumi Nakatomi, Nobuhito Saito
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Abstract

Background: White epidermoid cysts (WECs) are a rare type of epidermoid cyst with atypical radiological features. The epidemiological aspects and mechanisms of their onset remain unknown. Herein, the authors report a unique case of WEC transformation from a typical epidermoid cyst after stereotactic radiosurgery (SRS), confirmed by radiological and pathological findings.

Observations: The case involved a 78-year-old man with a history of 2 surgeries for a left cerebellopontine angle typical epidermoid cyst 23 years earlier and SRS using the CyberKnife for recurrent trigeminal neuralgia (TN) 14 years earlier. The tumor with high intensity on T1-weighted imaging, low intensity on T2-weighted imaging, without restriction on diffusion-weighted imaging had gradually enlarged after SRS. Therefore, a salvage surgery was performed via a left suboccipital craniotomy, and the intraoperative findings showed a cyst with a brown, viscous liquid component, consistent with those of WECs. Histopathologically, keratin calcification and hemorrhage were identified, leading to a diagnosis of WEC. The postoperative course was uneventful, and the TN resolved. No tumor recurrence was recorded at 2 years postoperatively.

Lessons: To the best of the authors' knowledge, this is the first world case of WEC transformation from a typical epidermoid cyst after SRS, confirmed by radiological and pathological findings. Radiation effects could have been involved in this transformation.

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立体定向放射外科治疗后白色表皮样囊肿的转化:一例说明。
背景:白色表皮样囊肿(WECs)是一种罕见的具有非典型放射学特征的表皮样囊肿。其发病的流行病学方面和机制仍然未知。在此,作者报告了一例经放射学和病理学证实的典型表皮样囊肿立体定向放射外科(SRS)后WEC转化的独特病例。观察:该病例涉及一名78岁的男性,23年前曾接受过2次左桥小脑角典型表皮样囊肿手术,14年前曾使用CyberKnife进行SRS治疗复发性三叉神经痛(TN)。SRS后,T1加权成像强度高、T2加权成像强度低、扩散加权成像无限制的肿瘤逐渐增大。因此,通过左侧枕下开颅术进行了挽救性手术,术中检查结果显示囊肿中有棕色粘稠液体成分,与WEC一致。组织病理学检查发现角蛋白钙化和出血,诊断为WEC。术后进展顺利,TN消失。术后2年无肿瘤复发记录。经验教训:据作者所知,这是世界上第一例SRS后典型表皮样囊肿转化为WEC的病例,经放射学和病理学检查证实。辐射效应可能参与了这种转变。
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