Elsherif Yasmine, Aziz Nouman, Nabi Waseem, Bhat Adnan, Basharat Ahmad, Nelli Fromer
Internal Medicine Department, Zayed Military Hospital, Abu Dhabi, UAE.
Internal Medicine Department, Wyckoff Heights Medical Center, Brooklyn, New York, USA.
Radiol Case Rep. 2025 May 1;20(7):3484-3496. doi: 10.1016/j.radcr.2025.03.070. eCollection 2025 Jul.
Primary CNS melanoma is an extremely rare and aggressive malignancy, especially in pediatric patients. We present the case of a 12-year-old girl who initially presented with sudden-onset severe headache and neurological deficits, and imaging revealed a left frontotemporal mass, suspected to be an arteriovenous malformation. After developing spontaneous intracerebral hemorrhage, she underwent emergency craniectomy and partial resection, with pathology confirming primary CNS melanoma. Despite treatment with immunotherapy, her condition deteriorated, leading to progressive hydrocephalus and leptomeningeal metastasis, ultimately resulting in her death. This case highlights the diagnostic and therapeutic challenges of primary CNS melanoma in children, emphasizing its rapid progression, limited treatment efficacy, and the need for early recognition, multidisciplinary management, and further research for definitive treatment.
原发性中枢神经系统黑色素瘤是一种极其罕见且侵袭性强的恶性肿瘤,在儿科患者中尤为如此。我们报告了一名12岁女孩的病例,她最初表现为突发严重头痛和神经功能缺损,影像学检查发现左侧额颞部肿块,怀疑是动静脉畸形。在发生自发性脑出血后,她接受了急诊开颅手术和部分切除术,病理证实为原发性中枢神经系统黑色素瘤。尽管接受了免疫治疗,她的病情仍恶化,导致进行性脑积水和软脑膜转移,最终死亡。该病例凸显了儿童原发性中枢神经系统黑色素瘤在诊断和治疗方面的挑战,强调了其进展迅速、治疗效果有限,以及早期识别、多学科管理和进一步确定性治疗研究的必要性。