Gold Justin, Hernandez Nick R, Wong Timothy, Patel Nitesh, Weiner Joseph, Hanft Simon
Department of Neurological Surgery, Cooper Medical of Rowan University, Camden, New Jersey, United States.
Department of Neurosurgery, Robert Wood Johnson Hospital, New Brunswick, New Jersey, United States.
Asian J Neurosurg. 2024 May 27;19(3):540-550. doi: 10.1055/s-0044-1787081. eCollection 2024 Sep.
Primary spinal malignant melanoma (PSMM) is a rare cancer of the central nervous system (CNS), and PSMM of the spinal nerve root is even more extraordinary. PSMM of a nerve root can mimic the radiographic appearance of benign nerve sheath tumors, thus resulting in misdiagnosis until tissue diagnosis can be made. A 53-year-old African American woman presented with pain primarily involving the left aspect of her neck and shoulder for 2 years. Magnetic resonance imaging (MRI) of the cervical spine demonstrated a T1-hyperintense, T2-hypointense, homogenously enhancing, dumbbell-shaped, intradural extramedullary mass extending out through the left C2-3 foramen. A midline incision was used to perform a C2 and C3 laminectomy, and the mass was removed from the cavity. The histopathologic profile was consistent with the diagnosis of malignant melanoma. The present case report adds to the 110 cases of PSMM and the 20 cases of PSMM of the spinal nerve root in the existing body of literature. Radiographic and clinical features resemble that of the much more common schwannoma or neurofibroma requiring immunohistochemical analysis for definitive diagnosis. The optimal treatment for PSMM has not yet been defined due to its rarity and it is therefore important to report such cases in order to share our clinical experiences and provide data to other clinicians treating this uncommon disease.
原发性脊髓恶性黑色素瘤(PSMM)是一种罕见的中枢神经系统(CNS)癌症,而神经根性PSMM更为罕见。神经根性PSMM在影像学上可类似良性神经鞘瘤,从而导致误诊,直至进行组织诊断。一名53岁的非裔美国女性,主要因颈部和肩部左侧疼痛2年就诊。颈椎磁共振成像(MRI)显示一个T1高信号、T2低信号、均匀强化的哑铃形硬膜内髓外肿块,经左侧C2-3椎间孔向外延伸。采用中线切口行C2和C3椎板切除术,并从腔内切除肿块。组织病理学特征符合恶性黑色素瘤的诊断。本病例报告补充了现有文献中110例PSMM和20例神经根性PSMM的病例。影像学和临床特征与更为常见的神经鞘瘤或神经纤维瘤相似,需要进行免疫组织化学分析以明确诊断。由于PSMM罕见,其最佳治疗方法尚未确定,因此报告此类病例很重要,以便分享我们的临床经验,并为治疗这种罕见疾病的其他临床医生提供数据。