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颅内中间级脑膜黑素细胞瘤伴细胞增殖指数增加:一例与太田痣相关的说明性病例。

Intracranial intermediate-grade meningeal melanocytoma with increased cellular proliferative index: an illustrative case associated with a nevus of Ota.

作者信息

Navas Marta, Pascual José M, Fraga Javier, Pedrosa Manuel, Shakur Sophia, Carrasco Rodrigo, Martínez Pedro, Manzanares Rafael, de Sola Rafael García

机构信息

Department of Neurosurgery, La Princesa University Hospital, C/Diego de León 62, 28006, Madrid, Spain.

Department of Pathology, La Princesa University Hospital, Madrid, Spain.

出版信息

J Neurooncol. 2009 Oct;95(1):105-115. doi: 10.1007/s11060-009-9907-3. Epub 2009 May 18.

DOI:10.1007/s11060-009-9907-3
PMID:19449182
Abstract

Solitary primary melanocytic tumors of the central nervous system (CNS) represent a spectrum of lesions ranging from well-differentiated melanocytoma to melanoma. The association of a meningeal melanocytoma with an ipsilateral nevus of Ota is extremely rare, with only six cases reported in the literature to date. Only a minority of melanocytic tumors correspond to lesions of intermediate-grade malignancy, whose biological behavior and outcome remain undetermined. We report a new case of a 25-year-old man with a giant fronto-temporal intracranial meningeal melanocytoma associated with a congenital nevus of Ota, who suffered an acute neurological deterioration requiring an emergent surgical procedure. Despite total removal of the lesion, the patient did not recover from the operation due to a malignant infarct of the right hemisphere. The lesion showed no histological criteria of malignancy but did exhibit an elevated (8%) MIB-1/Ki-67 cell proliferative index, which suggested an intermediate-grade melanocytoma. In addition, its metabolic profile, determined by in vivo proton magnetic resonance spectroscopy (MRS), was similar to that observed in most high-grade gliomas. To our knowledge, this is the first case of a meningeal melanocytoma of intermediate grade associated with a nevus of Ota reported in the literature. Only two additional intermediate-grade melanocytomas showing an elevated MIB-1/Ki-67 labeling index have been previously reported. The MIB-1/Ki-67 labeling index may have potential prognostic value in helping the clinician to predict an aggressive clinical behavior and/or malignant progression for primary melanocytic neoplasms of the CNS.

摘要

中枢神经系统(CNS)的孤立性原发性黑素细胞肿瘤代表了一系列病变,范围从高分化黑素细胞瘤到黑色素瘤。脑膜黑素细胞瘤与同侧太田痣相关极为罕见,迄今为止文献中仅报道了6例。只有少数黑素细胞肿瘤属于中度恶性病变,其生物学行为和预后仍不明确。我们报告了一例新病例,一名25岁男性患有巨大的额颞部颅内脑膜黑素细胞瘤并伴有先天性太田痣,该患者出现急性神经功能恶化,需要紧急手术。尽管病变已完全切除,但由于右半球恶性梗死,患者术后未能康复。该病变无恶性组织学标准,但MIB-1/Ki-67细胞增殖指数升高(8%),提示为中度黑素细胞瘤。此外,通过体内质子磁共振波谱(MRS)测定的其代谢谱与大多数高级别胶质瘤中观察到的相似。据我们所知,这是文献中报道的首例与太田痣相关的中度脑膜黑素细胞瘤。此前仅另外报道了两例MIB-1/Ki-67标记指数升高的中度黑素细胞瘤。MIB-1/Ki-67标记指数在帮助临床医生预测中枢神经系统原发性黑素细胞肿瘤的侵袭性临床行为和/或恶性进展方面可能具有潜在的预后价值。

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