Ogose A, Hotta T, Morita T, Otsuka H, Hirata Y
Niigata Cancer Centre Hospital and Niigata University, Japan.
J Bone Joint Surg Br. 1998 Jul;80(4):657-61. doi: 10.1302/0301-620x.80b4.8532.
Multiple tumours of peripheral nerves are often seen in patients with neurofibromatosis of type 1 or 2. Multiple schwannomas may occur without other manifestations of neurofibromatosis. We have reviewed 12 patients with multiple schwannomas arising from peripheral lesions who did not fulfil the criteria for either type of neurofibromatosis. Four had spinal and one an intracranial lesion in addition to the peripheral tumours. Two patients had one and three café-au-lait spots, respectively, and another had a probable family history. The largest tumours were 45 to 250 mm in size. Three patients had been referred as having von Recklinghausen's disease. The large size of tumours, the difficulties of histological diagnosis on biopsy, and the confusion with neurofibromatosis can lead to overtreatment. Malignant change seldom, if ever, occurs in patients with multiple schwannomas.
多发性周围神经肿瘤常见于1型或2型神经纤维瘤病患者。多发性施万细胞瘤可在无神经纤维瘤病其他表现的情况下发生。我们回顾了12例源于周围病变的多发性施万细胞瘤患者,他们不符合任何一种神经纤维瘤病的诊断标准。除周围肿瘤外,4例有脊柱病变,1例有颅内病变。2例患者分别有1个和3个咖啡牛奶斑,另1例可能有家族史。最大的肿瘤大小为45至250毫米。3例患者被诊断为冯雷克林霍增氏病。肿瘤体积大、活检组织学诊断困难以及与神经纤维瘤病的混淆可导致过度治疗。多发性施万细胞瘤患者很少发生恶变。