Primary meningeal melanocytoma of cerebellopontine angle: A case report with 12 years follow up

Sushila Jaiswal, Awadhesh Kumar Jaiswal, Mukul Vij, Sanjay Behari, Rakesh Pandey
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引用次数: 2

Abstract

The authors describe a case of cerebellopontine (CP) angle melanotic lesion in a 38-year-old man who presented with features of CP angle syndrome 12 years ago. Computed tomography scan showed a mass lesion in the left CP angle, which was excised. Biopsy was suggestive of melanoma due to abundance of melanin. After 12 years, he had local recurrence and was re-operated. On reviewing the previous and later biopsy, final diagnosis of melanocytoma was made because of additional finding of absence of mitosis and macronucleoli, which were overlooked in the previous biopsy. Awareness of this finding reduces the possibility of diagnostic error in melanotic tumors. Reliance on the presence of abundance of melanin as the sole criterion for diagnosing melanoma resulted in erroneous diagnosis in our case. The case is discussed in the light of available literature.

脑桥小脑角原发性脑膜黑素细胞瘤1例,随访12年
作者描述了一个38岁男性脑桥小脑(CP)角黑色素病变的病例,他在12年前出现了CP角综合征的特征。计算机断层扫描显示左侧CP角肿块病变,已切除。由于黑色素丰富,活检提示黑色素瘤。12年后,他局部复发,再次手术。回顾之前和之后的活检,最终诊断为黑素细胞瘤,因为在之前的活检中忽略了有丝分裂和大核桃核的缺失。对这一发现的认识减少了黑色素瘤诊断错误的可能性。在我们的病例中,依赖黑色素丰富的存在作为诊断黑色素瘤的唯一标准导致了错误的诊断。根据现有文献对该案例进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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