Javed Saad, Khan Amina, Khalid Ayesha, Scalia Gianluca, Umana Giuseppe Emmanuele, Mahmood Ashraf, Yaqoob Eesha, Pahwa Bhavya, Chaurasia Bipin
Department of Neurosurgery Rawalpindi Medical University Rawalpindi Pakistan.
Department of Neurosurgery Rawalpindi Medical University Rawalpindi Rawalpindi Pakistan.
Clin Case Rep. 2024 Apr 26;12(5):e8789. doi: 10.1002/ccr3.8789. eCollection 2024 May.
Scalp metastasis from atypical meningioma, though rare, underscores the importance of meticulous surgical techniques to prevent tumor cell implantation. Early detection and comprehensive management, including surgery and adjuvant therapy, are crucial for optimal outcomes.
Meningiomas are tumors of the meninges that originate in the arachnoid layer from arachnoid cap cells. Atypical meningiomas, classified as WHO grade 2 tumors, tend to metastasize and recur if not surgically managed properly. Scalp metastasis is a rare occurrence that presents as a subcutaneous elevation. A 33-year-old patient presented with a complaint of a constant, dull pressure headache persisting for the past 12 months, exacerbated by exertion, along with seizures and neuropsychiatric symptoms. The patient had no significant medical history but had undergone surgery 4 years ago for a WHO grade 2 meningioma. The current brain MRI revealed a dural tail sign, along with masses on both the left and right sides of the frontal lobe, extending to involve the skin on the forehead and scalp. The patient underwent surgical resection and adjuvant radiation therapy. At the 12-month follow-up, no neurological deterioration or tumor recurrence was observed. A literature review on scalp metastasis in patients with atypical meningioma was also conducted, including eight articles published up to September 2023. The mechanism of metastasis development appears to be consistent in all eight reported cases, involving the implantation of tumor cells during resection. Therefore, there is a critical need for meticulous intra- and post-operative surgical techniques to prevent such implantation.
非典型脑膜瘤的头皮转移虽罕见,但凸显了精细手术技术对防止肿瘤细胞种植的重要性。早期检测及包括手术和辅助治疗在内的综合管理对于取得最佳治疗效果至关重要。
脑膜瘤是起源于蛛网膜层蛛网膜帽细胞的脑膜肿瘤。非典型脑膜瘤被归类为世界卫生组织2级肿瘤,若手术处理不当往往会发生转移和复发。头皮转移是一种罕见情况,表现为皮下隆起。一名33岁患者主诉持续钝性压迫性头痛已持续12个月,劳累后加重,伴有癫痫发作和神经精神症状。该患者无重大病史,但4年前因世界卫生组织2级脑膜瘤接受过手术。目前的脑部磁共振成像显示有硬脑膜尾征,额叶左右两侧有肿块,延伸至前额和头皮的皮肤。患者接受了手术切除和辅助放疗。在12个月的随访中,未观察到神经功能恶化或肿瘤复发。还对非典型脑膜瘤患者的头皮转移进行了文献综述,包括截至2023年9月发表的8篇文章。在所有8例报告病例中,转移发生机制似乎一致,均涉及切除过程中肿瘤细胞的种植。因此,迫切需要精细的术中和术后手术技术来防止此类种植。