Primary intracranial malignant melanoma in an adolescent: case report and literature review

Primary intracranial malignant melanoma (PIMM) is an exceedingly rare central nervous system tumor, accounting for only 1% of melanoma cases and 0.07% of primary CNS tumors, with limited documentation in adolescents. This case report describes an 18-year-old male who presented with a seizure, markin...

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Main Authors: Nyoman Golden, I Gusti Ketut Agung Surya Kencana, Christopher Lauren, Angky Saputra, Denny Japardi
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-02-01
Series:Frontiers in Surgery
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Online Access:https://www.frontiersin.org/articles/10.3389/fsurg.2025.1524204/full
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author Nyoman Golden
I Gusti Ketut Agung Surya Kencana
Christopher Lauren
Angky Saputra
Denny Japardi
author_facet Nyoman Golden
I Gusti Ketut Agung Surya Kencana
Christopher Lauren
Angky Saputra
Denny Japardi
author_sort Nyoman Golden
collection DOAJ
description Primary intracranial malignant melanoma (PIMM) is an exceedingly rare central nervous system tumor, accounting for only 1% of melanoma cases and 0.07% of primary CNS tumors, with limited documentation in adolescents. This case report describes an 18-year-old male who presented with a seizure, marking the onset of his symptoms. Following an emergency assessment, MRI identified a heterogeneous mass in the right parasagittal frontal region, initially misdiagnosed as a cystic meningioma. A craniotomy allowed for total tumor resection, and histopathological analysis revealed a malignant melanoma characterized by neoplastic cells with pronounced nuclear pleomorphism and significant mitotic activity. Postoperative evaluations, including a PET scan, confirmed no extracranial melanoma, affirming the diagnosis of primary CNS melanoma. The patient demonstrated no neurological deficits or seizures one year post-surgery and was managed with adjuvant radiotherapy. This report emphasizes the necessity of considering PIMM in differential diagnoses for seizures in young patients and highlights the importance of comprehensive diagnostic evaluations, including MRI and histopathology, in rare cases. Additionally, the findings underscore the critical role of complete surgical resection in improving outcomes, with adjuvant therapies potentially enhancing long-term management and surveillance. As PIMM presents with nonspecific symptoms, awareness among clinicians is essential for early detection and appropriate intervention, warranting further research to develop standardized treatment protocols and enhance understanding of this rare tumor's pathophysiology.
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spelling doaj-art-cbeb4e66f0ab4fe395d6ec5a62e77fcc2025-02-10T15:06:01ZengFrontiers Media S.A.Frontiers in Surgery2296-875X2025-02-011210.3389/fsurg.2025.15242041524204Primary intracranial malignant melanoma in an adolescent: case report and literature reviewNyoman GoldenI Gusti Ketut Agung Surya KencanaChristopher LaurenAngky SaputraDenny JapardiPrimary intracranial malignant melanoma (PIMM) is an exceedingly rare central nervous system tumor, accounting for only 1% of melanoma cases and 0.07% of primary CNS tumors, with limited documentation in adolescents. This case report describes an 18-year-old male who presented with a seizure, marking the onset of his symptoms. Following an emergency assessment, MRI identified a heterogeneous mass in the right parasagittal frontal region, initially misdiagnosed as a cystic meningioma. A craniotomy allowed for total tumor resection, and histopathological analysis revealed a malignant melanoma characterized by neoplastic cells with pronounced nuclear pleomorphism and significant mitotic activity. Postoperative evaluations, including a PET scan, confirmed no extracranial melanoma, affirming the diagnosis of primary CNS melanoma. The patient demonstrated no neurological deficits or seizures one year post-surgery and was managed with adjuvant radiotherapy. This report emphasizes the necessity of considering PIMM in differential diagnoses for seizures in young patients and highlights the importance of comprehensive diagnostic evaluations, including MRI and histopathology, in rare cases. Additionally, the findings underscore the critical role of complete surgical resection in improving outcomes, with adjuvant therapies potentially enhancing long-term management and surveillance. As PIMM presents with nonspecific symptoms, awareness among clinicians is essential for early detection and appropriate intervention, warranting further research to develop standardized treatment protocols and enhance understanding of this rare tumor's pathophysiology.https://www.frontiersin.org/articles/10.3389/fsurg.2025.1524204/fullmalignant melanomamalignant neoplasmneurosurgical proceduresoncologytumor
spellingShingle Nyoman Golden
I Gusti Ketut Agung Surya Kencana
Christopher Lauren
Angky Saputra
Denny Japardi
Primary intracranial malignant melanoma in an adolescent: case report and literature review
Frontiers in Surgery
malignant melanoma
malignant neoplasm
neurosurgical procedures
oncology
tumor
title Primary intracranial malignant melanoma in an adolescent: case report and literature review
title_full Primary intracranial malignant melanoma in an adolescent: case report and literature review
title_fullStr Primary intracranial malignant melanoma in an adolescent: case report and literature review
title_full_unstemmed Primary intracranial malignant melanoma in an adolescent: case report and literature review
title_short Primary intracranial malignant melanoma in an adolescent: case report and literature review
title_sort primary intracranial malignant melanoma in an adolescent case report and literature review
topic malignant melanoma
malignant neoplasm
neurosurgical procedures
oncology
tumor
url https://www.frontiersin.org/articles/10.3389/fsurg.2025.1524204/full
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AT christopherlauren primaryintracranialmalignantmelanomainanadolescentcasereportandliteraturereview
AT angkysaputra primaryintracranialmalignantmelanomainanadolescentcasereportandliteraturereview
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