Piercecchi-Marti Marie-Dominique, Mohamed Hicham, Liprandi Agnes, Gambarelli Daniele, Grisoli Francois, Pellissier Jean-François
Department of Forensic Medicine, Centre Hospitalier Régional et Universitaire de Marseille, Timone, France.
J Neurosurg. 2002 Mar;96(3):619-23. doi: 10.3171/jns.2002.96.3.0619.
In this report, the authors review the case of a man with a neurocutaneous syndrome. He presented with an intracerebral melanocytoma associated with a blue nevus of the scalp; its location and its appearance during childhood supported the diagnosis of a nevus of Ota. Meningeal melanocytomas are increasingly being diagnosed, but remain rare. Primary meningeal malignant melanoma is the first differential diagnosis to eliminate. Despite their common embryonic origin. the association of a melanocytoma with a nevus of Ota is rare. A nevus of Ota exhibits the same melanocytic proliferation and affects the trigeminal nerve territory. An ocular effect is not always observed. In contrast to an ocular lesion, a nevus of Ota rarely transforms into a malignant melanoma. It is found only among caucasians. During 4 years of follow-up review after surgery, the patient remained asymptomatic. Other than antiepileptic therapy, he received no complementary treatment and cerebral imaging revealed no evidence of recurrence.
在本报告中,作者回顾了一例患有神经皮肤综合征的男性病例。他表现为颅内黑素细胞瘤,伴有头皮蓝色痣;其位置及童年期外观支持太田痣的诊断。脑膜黑素细胞瘤的诊断越来越多,但仍然罕见。原发性脑膜恶性黑色素瘤是首先要排除的鉴别诊断。尽管它们有共同的胚胎起源,但黑素细胞瘤与太田痣的关联很少见。太田痣表现出相同的黑素细胞增殖,并累及三叉神经分布区域。并非总能观察到眼部影响。与眼部病变不同,太田痣很少转变为恶性黑色素瘤。它仅在白种人中发现。术后4年的随访复查期间,患者无症状。除抗癫痫治疗外,他未接受其他辅助治疗,脑部影像学检查未发现复发迹象。