Matsumoto Hideki, Shinya Yuki, Miyawaki Satoru, Shin Masahiro, Koizumi Satoshi, Sato Daisuke, Hinata Munetoshi, Ikemura Masako, Kiyofuji Satoshi, Kin Taich, Iwanaga Mototaro, Shimizu Masahiro, Nakatomi Hirofumi, Saito Nobuhito
Departments of1Neurosurgery and.
2Department of Neurosurgery, Teikyo University Hospital, Tokyo, Japan.
J Neurosurg Case Lessons. 2023 Jun 12;5(24). doi: 10.3171/CASE2376.
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.
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.
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.
白色表皮样囊肿(WECs)是一种罕见的表皮样囊肿,具有非典型的放射学特征。其流行病学情况及发病机制尚不清楚。在此,作者报告了一例经立体定向放射外科治疗(SRS)后由典型表皮样囊肿转变为WEC的独特病例,经放射学和病理学检查得以证实。
该病例为一名78岁男性,23年前因左侧桥小脑角典型表皮样囊肿接受过2次手术,14年前因复发性三叉神经痛(TN)使用射波刀进行了SRS治疗。T1加权成像上呈高信号、T2加权成像上呈低信号、弥散加权成像无受限的肿瘤在SRS后逐渐增大。因此,通过左枕下开颅进行了挽救性手术,术中发现一个含有棕色粘性液体成分的囊肿,与WECs一致。组织病理学检查发现有角质钙化和出血,从而诊断为WEC。术后病程顺利,TN症状缓解。术后2年未记录到肿瘤复发。
据作者所知,这是世界上首例经放射学和病理学检查证实的SRS后由典型表皮样囊肿转变为WEC的病例。这种转变可能与放射效应有关。