Li Chao, Fowler James, Balasubramanian Kishore, Fung Kar-Ming, Zhe Piao, Wu William W
Department of Neurosurgery, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Department of Neurosurgery, Hartford Hospital, Hartford, Connecticut.
J Neurol Surg Rep. 2025 Apr 3;86(2):e57-e64. doi: 10.1055/a-2547-5320. eCollection 2025 Apr.
Although malignant transformation of benign vestibular schwannoma (VS) preceded by irradiation has been well documented, few studies have demonstrated malignant transformation in the absence of radiation. Here, we present a rare case of the malignant transformation of a benign VS to a malignant peripheral nerve sheath tumor (MPNST) in the absence of prior irradiation. Additionally, we conducted a literature search to identify all other reported cases of MPNST arising from VS under similar conditions.
A 75-year-old female presented to the hospital with a 1-month history of left-sided facial numbness, loss of taste on the left side of her tongue, severe dysarthria, and recent-onset cranial nerve VI and VII palsies. MRI of the brain with and without contrast demonstrated an enlarging cerebellopontine angle mass and signs of brainstem compression. The patient underwent a left retrosigmoid craniotomy and surgical resection. Pathology and immunohistochemistry sequencing findings were consistent for MPNST with rhabdomyoblastic differentiation (malignant triton tumor). An outside review of the case by a large academic institution concurred with the diagnosis. The patient did not report any previous history of irradiation.
A total of 11 cases, including ours, have appropriate S-100 immunochemical reactivity to confirm malignant transformation. Due to the limited number of reported cases of MPNST arising from VS without prior irradiation, information regarding pathogenesis and pathological diagnosis is scarce. We provide valuable additions to the literature, including next-generation sequencing data, to identify potentially targetable genetic changes and help elucidate the pathogenesis of MPNST.
尽管已有充分文献记载良性前庭神经鞘瘤(VS)在放疗后发生恶变,但很少有研究表明在无放疗情况下会发生恶变。在此,我们报告一例罕见的良性VS在无既往放疗史的情况下恶变为恶性外周神经鞘瘤(MPNST)的病例。此外,我们进行了文献检索,以确定所有其他在类似情况下报道的源自VS的MPNST病例。
一名75岁女性因左侧面部麻木1个月、左侧舌味觉丧失、严重构音障碍及近期出现的颅神经VI和VII麻痹入院。头颅MRI平扫及增强显示桥小脑角区肿块增大及脑干受压征象。患者接受了左乙状窦后开颅手术及肿瘤切除术。病理及免疫组化测序结果符合伴有横纹肌母细胞分化的MPNST(恶性蝾螈瘤)。一家大型学术机构对该病例的外部评估与诊断结果一致。患者未报告既往放疗史。
包括我们的病例在内,共有11例病例具有适当的S-100免疫化学反应以证实恶变。由于报道的无既往放疗史的源自VS的MPNST病例数量有限,关于其发病机制和病理诊断的信息稀缺。我们为文献提供了有价值的补充内容,包括二代测序数据,以识别潜在的可靶向基因改变并有助于阐明MPNST的发病机制。