Robitaille Y, Seemayer T A, El Deiry A
Cancer. 1975 Apr;35(4):1254-8. doi: 10.1002/1097-0142(197504)35:4<1254::aid-cncr2820350433>3.0.co;2-3.
A 45-year-old man, afflicted with von Recklinghausen's disease, with symptomatic schwannomas and plexiform neurofibromas involving the right maxillary antrum, a rare site for peripheral nerve tumors, is presented. After a literature review, 15 cases were considered adequate for a clinicopathologic study. Twelve schwannomas, 2 plexiform neurofibromas, 2 neurofibromas, and 1 probable malignant schwannoma were included. Epistaxis was common in tumors of the ethmoid sinus and nasal fossae, while pain was related to lesions of the maxillary sinus. Two benign schwannomas recurred and were cured by surgery alone. The importance of early diagnosis and thorough surgical excisions is emphasized, especially for those tumors associated with von Recklinghausen's disease. The difficulties involved in the diagnosis of primary malignant peripheral nerve tumors are discussed.
本文报告了一名45岁患有冯雷克林霍增氏病的男性,其症状性神经鞘瘤和丛状神经纤维瘤累及右上颌窦,这是周围神经肿瘤的一个罕见部位。经文献回顾,15例病例适合进行临床病理研究。其中包括12例神经鞘瘤、2例丛状神经纤维瘤、2例神经纤维瘤和1例可能的恶性神经鞘瘤。鼻出血在筛窦和鼻窝肿瘤中常见,而疼痛与上颌窦病变有关。2例良性神经鞘瘤复发,仅通过手术治愈。强调了早期诊断和彻底手术切除的重要性,尤其是对于那些与冯雷克林霍增氏病相关的肿瘤。还讨论了原发性恶性周围神经肿瘤诊断中存在的困难。