Chance Aaron, Liu Jesse J, Raskin Jeffrey S, Zherebitskiy Viktor, Gultekin Sakir H, Raslan Ahmed M
University of Texas Medical School, Houston, Texas; and
Departments of 2 Neurological Surgery and.
J Neurosurg Spine. 2015 Dec;23(6):780-3. doi: 10.3171/2015.3.SPINE141265. Epub 2015 Aug 21.
Complex neurocristopathy, a disorder resulting from the aberrant proliferation of tissues derived from neural crest cells, has been previously reported in 2 patients, both involving ophthalmic melanoma and other tumors. One patient had a periorbital neurofibroma, sphenoid wing meningioma, and choroid juxtapapillary meningioma. The other patient had a choroidal melanoma and an optic nerve sheath meningioma. The authors describe clinical and pathological findings in a patient who underwent resection of 2 distinct lesions: primary CNS melanoma at T-12 and an L-5 schwannoma. Clinical and histopathological findings of the case are reviewed. To the authors' knowledge, this is the first patient to present with complex neurocristopathy involving both a spinal melanoma and schwannoma.
复杂神经嵴病变是一种由神经嵴细胞衍生组织异常增殖引起的疾病,此前曾在2例患者中报道过,均涉及眼黑色素瘤和其他肿瘤。1例患者患有眶周神经纤维瘤、蝶骨嵴脑膜瘤和脉络膜乳头旁脑膜瘤。另1例患者患有脉络膜黑色素瘤和视神经鞘脑膜瘤。作者描述了1例接受2个不同病变切除手术患者的临床和病理结果:T-12节段的原发性中枢神经系统黑色素瘤和L-5节段的神经鞘瘤。对该病例的临床和组织病理学结果进行了回顾。据作者所知,这是首例出现涉及脊髓黑色素瘤和神经鞘瘤的复杂神经嵴病变的患者。