Kasuya H, Kadowaki H, Yato S, Kubo O, Kagawa M, Kitamura K
Neurosurgery. 1986 Feb;18(2):207-11.
A patient who presented with a tumor of the left ambient cistern, a left cerebellopontine angle tumor, and a left orbital tumor causing left hearing loss and left exophthalmos without café au lait spots or cutaneous neurofibromas is described. There was no family history of von Recklinghausen's disease. A cerebellopontine angle tumor removed by a suboccipital craniectomy was an acoustic neurinoma. An ambient cistern tumor was approached through a subtemporal route. A tumor arising from the trigeminal nerve was also a neurinoma. An orbital neurofibroma was excised by a frontal craniotomy with removal of the orbital roof. This rare unilateral association of neurinomas and a neurofibroma on the left side was thought to be a forme fruste of von Recklinghausen's disease, and it could be considered a presentation of a mosaic of von Recklinghausen's disease.
本文描述了一名患者,其左环池有肿瘤、左小脑桥脑角有肿瘤以及左眼眶有肿瘤,导致左耳听力丧失和左眼球突出,且无牛奶咖啡斑或皮肤神经纤维瘤。患者无冯雷克林霍增氏病家族史。经枕下颅骨切除术切除的小脑桥脑角肿瘤为听神经瘤。通过颞下途径处理环池肿瘤。起源于三叉神经的肿瘤也是神经鞘瘤。经额开颅术切除眶顶后切除眼眶神经纤维瘤。这种左侧神经鞘瘤和神经纤维瘤罕见的单侧关联被认为是冯雷克林霍增氏病的顿挫型,可视为冯雷克林霍增氏病的一种镶嵌表现形式。