Rahimi-Movaghar Vafa, Karimi Mehrbod
Department of Neurosurgery, Khatam-ol-anbia Hospital, Zahedan University of Medical Sciences, Zahedan, Iran.
Surg Neurol. 2003 Mar;59(3):200-10. doi: 10.1016/s0090-3019(02)01052-2.
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.
脑膜黑素细胞瘤是一种罕见的脑膜黑素细胞良性色素性肿瘤。太田痣是巩膜及眼周皮肤的黑素细胞色素沉着。我们报告一例罕见的伴有同侧黏膜皮肤黑变病的顶叶凸面脑膜黑素细胞瘤,并对相关文献进行复习。
一名17岁男性患者,出现头痛和失明症状。左侧头皮及面部有黏膜皮肤黑变病。手术过程中,在头皮、颅骨、硬脑膜甚至室管膜的各层均可见散在的色素沉着。对肿瘤及头皮进行病理检查,包括光学显微镜检查和免疫组织化学检查。在文献复习中,分析了患者的人口统计学特征(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)以及预后(复发、死亡、与疾病相关的死亡以及随访情况)。统计学分析采用独立样本t检验和卡方检验。
已报道95例脑膜黑素细胞瘤病例(45例颅内病变和50例脊髓病变)。颅内病变患者的中位年龄(40岁)显著低于脊髓病变患者(49岁)(p = 0.016)。95例患者中,57.9%为女性。在神经系统中,黑素细胞在幕下和颈部区域更为常见,但超过半数的肿瘤位于幕上区域和胸椎。中位随访46个月时,肿瘤复发率和肿瘤相关死亡率分别为26.3%和10.5%。不同治疗方式之间这些差异无统计学意义。与其他组相比,未接受放疗而行肿瘤次全切除的患者生存时间有缩短趋势。
结合相关文献复习,对脑膜黑素细胞瘤的预后标准、鉴别诊断及胚胎学方面进行了讨论。