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Meningeal melanocytoma of the brain and oculodermal melanocytosis (nevus of ota): case report and literature review.

机译:脑部脑膜黑素细胞瘤和眼皮黑素细胞增多症(太田痣):病例报告和文献复习。

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Meningeal melanocytomas are rare benign pigmented tumors of meningeal melanocytes. Nevus of Ota is a melanocytic pigmentation of the sclera and the skin adjacent to the eye. We report a rare case of parietal convexity meningeal melanocytoma associated with ipsilateral mucocutaneous melanosis and review the literature.A 17-year-old man presented with headache and blindness. There was left scalp and facial mucocutaneous melanosis. During surgery, speckled hyperpigmentation was seen in all layers of the scalp, bone, dura, and even ependyma. Pathologic examination of the tumor and scalp consisted of light microscopy and immunohistochemistry. In a literature review, the demographics (age, sex), clinical characteristics (site of lesion, duration of symptoms), therapeutic options (surgical excision, radiotherapy), and prognosis (recurrence, death, death related to the disease, and follow-up) were analyzed. For statistical analysis we used the independent sample t-test and chi(2) tests.Ninety-five cases (45 intracranial and 50 spinal) of meningeal melanocytoma have been reported. The median age of patients with intracranial lesions (40 years) was significantly lower than that of patients with spinal lesions (49 years) (p = 0.016). Of the 95 patients, 57.9% were female. In the nervous system, melanocytes are more common in the infratentorial and cervical areas, but more than half of the tumors have been located in the supratentorial region and the thoracic spine. In 46 months median follow-up, tumor recurrence rate and tumor related death rate were 26.3% and 10.5%, respectively. These were not statistically significant for different therapeutic modalities. There was a trend toward shorter survival for patients who underwent subtotal tumor resection without radiotherapy compared with other groups.The prognostic criteria, differential diagnosis, and the embryological aspects of meningeal melanocytoma are discussed with a review of the related literature.
机译:脑膜黑素细胞瘤是罕见的脑膜黑素细胞良性色素沉着肿瘤。大田痣是巩膜和眼睛附近皮肤的黑素细胞色素沉着。我们报告了罕见的同侧粘膜皮肤黑色素沉着相关的顶叶凸性脑膜黑素细胞瘤病例,并复习了文献.17岁的男性出现头痛和失明。左侧头皮和面部粘膜皮肤黑色素沉着。在手术过程中,在头皮,骨骼,硬脑膜甚至室管膜的所有层均可见斑点状的色素沉着。肿瘤和头皮的病理检查包括光学显微镜和免疫组织化学。在文献综述中,人口统计学(年龄,性别),临床特征(病变部位,症状持续时间),治疗选择(手术切除,放疗)和预后(复发,死亡,与疾病相关的死亡以及随访)向上)进行了分析。为了进行统计分析,我们使用了独立样本t检验和chi(2)检验。已报告了95例(颅内45例,脊髓50例)脑膜黑素细胞瘤。颅内病变患者的中位年龄(40岁)显着低于脊髓病变患者的中位年龄(49岁)(p = 0.016)。在95名患者中,女性占57.9%。在神经系统中,黑素细胞在下腹和宫颈区域更为常见,但一半以上的肿瘤位于上上皮区和胸椎。在46个月的中位随访中,肿瘤复发率和与肿瘤相关的死亡率分别为26.3%和10.5%。这些对于不同的治疗方式没有统计学意义。与其他组相比,未经放射治疗而进行了次全切除术的患者的生存期有缩短的趋势。通过回顾相关文献讨论了脑膜黑素细胞瘤的预后标准,鉴别诊断和胚胎学方面。

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