Hussain Namath S, Specht Charles S, Frauenhoffer Elizabeth, Glantz Michael, Harbaugh Kimberly
Department of Neurosurgery, Penn State Hershey Medical Center.
Pathology, Penn State Hershey Medical Center.
Cureus. 2016 Mar 30;8(3):e548. doi: 10.7759/cureus.548.
Neurofibromas and schwannomas are common lesions that may be idiopathic or may occur in association with neural crest genetic syndromes such as neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. A hybrid tumor that contains pathological characteristics of both neurofibroma and schwannoma has been described as a rare entity. We present the clinical, radiographic, and pathological findings of such a case.
神经纤维瘤和神经鞘瘤是常见的病变，可能是特发性的，也可能与神经嵴遗传综合征相关，如1型神经纤维瘤病、2型神经纤维瘤病和神经鞘瘤病。一种兼具神经纤维瘤和神经鞘瘤病理特征的混合性肿瘤已被描述为一种罕见的实体。我们展示了这样一个病例的临床、影像学和病理结果。
