Demetriades Andreas K, Saunders Nicholas, Rose Peter, Fisher Cyril, Rowe Jeremy, Tranter Robert, Hardwidge Carl
Department of Neurosurgery, Hurstwood Park Neurological Centre, Brighton and Sussex University Hospitals, London, United Kingdom.
Skull Base. 2010 Sep;20(5):381-7. doi: 10.1055/s-0030-1253576.
Only a handful of cases of de-novo malignancies of the vestibulocochlear nerve have been reported. Even rarer is the malignant transformation of a previously histologically diagnosed benign vestibular schwannoma. We present the case of a young adult who had combined operative/Gamma knife treatment for a benign vestibular schwannoma, followed by further surgery 2 years later. He represented 10 years after original diagnosis with facial numbness and ataxia, MRI showing gross tumor recurrence. After radical resection, histology showed malignant transformation to a malignant peripheral nerve sheath tumor. Within 3 months there was rapid, aggressive recurrence with brainstem compression, requiring further surgery for brainstem decompression. Histology confirmed further de-differentiation to an anaplastic sarcoma. While awaiting radiotherapy the tumor recurred again, the patient succumbing. The patient had no features of neurofibromatosis type 2. In the literature there are 13 other cases of malignant vestibular schwannomata. Only six had radiotherapy and of these only two had histological confirmation of a benign lesion preradiotherapy. Neither of these had neurofibromatosis. Three other cases had histological proof of malignancy postradiosurgery, but with no preradiotherapy histology; of these, two were positive for neurofibromatosis. The tumor biology of vestibular schwannomata as well as the radiobiology in the context of malignant transformation is discussed.
仅报道过少数几例原发性前庭蜗神经恶性肿瘤。而先前经组织学诊断为良性的前庭神经鞘瘤发生恶性转化则更为罕见。我们报告了一例年轻成人病例,该患者曾接受手术联合伽玛刀治疗良性前庭神经鞘瘤,两年后又接受了进一步手术。他在最初诊断10年后出现面部麻木和共济失调,MRI显示肿瘤明显复发。根治性切除术后,组织学检查显示已恶变为恶性外周神经鞘膜瘤。3个月内肿瘤迅速侵袭性复发并压迫脑干,需要进一步手术以解除脑干压迫。组织学检查证实肿瘤进一步去分化为间变性肉瘤。在等待放疗期间肿瘤再次复发,患者最终死亡。该患者无2型神经纤维瘤病的特征。文献中还有其他13例恶性前庭神经鞘瘤病例。只有6例接受了放疗,其中只有2例在放疗前有良性病变的组织学证实。这两例均无神经纤维瘤病。另外3例在放射外科手术后有恶性肿瘤的组织学证据,但放疗前无组织学检查;其中2例神经纤维瘤病呈阳性。本文讨论了前庭神经鞘瘤的肿瘤生物学以及恶性转化背景下的放射生物学。