CC BY-NC-ND 4.0 · Asian J Neurosurg 2011; 6(02): 110-112
DOI: 10.4103/1793-5482.92176
CASE REPORT

Spinal meningeal melanocytoma

Rajeev Sen
Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana
,
Divya Sethi
Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana
,
Vandana Goyal
Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana
,
Amrita Duhan
Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana
,
Shilpi Modi
Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana
› Author Affiliations

Primary melanotic meningeal neoplasms are extremely rare lesions and benign forms are even rarer though with better prognosis than the malignant ones. We describe a 40-year-old male with a history of gradually progressive weakness of both lower limbs with normal bowel, bladder control, and an intradural mass measuring 1.5×1.0 cm on radiologic investigations. The lesion was surgically excised. Histopathologic examination revealed heavily melanin-pigmented cells, nuclei with reticulogranular chromatin and small nucleoli, moderate amount of eosinophillic cytoplasm with indistinct cell boundaries, and symplasmic appearance. A probable diagnosis of meningeal melanocytoma was made. The diagnosis was confirmed on immunohistochemical analysis which revealed strongly positive expression of HMB-45 in the tumor cells. Vimentin and S-100 were also diffusely positive while neuron specific enolase showed focal and patchy positivity; however, epithelial membrane antigen was distinctly negative.



Publication History

Article published online:
27 September 2022

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