Zhang Simin, Wang Weina, Su Xiaorui, Tan Qiaoyue, Sun Huaiqiang, Liu Zefan, Chen Ni, Gong Qiyong, Yue Qiang
Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital of Sichuan University, Chengdu, China.
Department of Oncology, West China Hospital of Sichuan University, Chengdu, China.
World Neurosurg. 2019 Feb;122:229-239. doi: 10.1016/j.wneu.2018.10.199. Epub 2018 Nov 4.
Meningeal melanoma is a rare tumor of the central nervous system, whose amelanotic variant is called "amelanotic meningeal melanoma" (AMM). AMM does not produce melanin and therefore does not exhibit typical short T1 and short T2 signal on magnetic resonance imaging and thus can be easily misdiagnosed and be inappropriately managed. To date, only 4 AMM cases have been reported in the English literature. Here, we report the fifth case.
A 26-year-old female patient presented with a 4-month history of progressive headache and nausea, the conventional magnetic resonance imaging demonstrated a posterior fossa mass accompanied by diffuse leptomeningeal dissemination. Repeated cerebrospinal fluid cytology screening showed negative results. The functional magnetic resonance examinations, including diffusion-weighted imaging, proton magnetic resonance spectroscopy, and dynamic susceptibility contrast perfusion-weighted imaging, provided complementary information. The final diagnosis of AMM was made by immunohistochemistry. Despite gross total excision of the tumor, the disease progressed, and the patient died 10 months after diagnosis.
Our experience with this case demonstrated that meningeal melanoma should be included in the differential diagnosis when an intracranial mass is accompanied by leptomeningeal dissemination, and especially when proton magnetic resonance spectroscopy and dynamic susceptibility contrast perfusion-weighted imaging indicate a malignant tumor whereas diffusion-weighted imaging does not. And the loss of a typical melanin signal should not server as an excluding criterion for meningeal melanoma.
脑膜黑色素瘤是一种罕见的中枢神经系统肿瘤,其无黑色素变异型被称为“无黑色素性脑膜黑色素瘤”(AMM)。AMM不产生黑色素,因此在磁共振成像上不表现出典型的短T1和短T2信号,从而容易被误诊和处理不当。迄今为止,英文文献中仅报道了4例AMM病例。在此,我们报告第5例病例。
一名26岁女性患者有4个月进行性头痛和恶心病史,常规磁共振成像显示后颅窝肿块并伴有弥漫性软脑膜播散。反复脑脊液细胞学筛查结果均为阴性。功能磁共振检查,包括扩散加权成像、质子磁共振波谱和动态磁敏感对比灌注加权成像,提供了补充信息。最终通过免疫组织化学确诊为AMM。尽管肿瘤进行了全切除,但疾病仍进展,患者在诊断后10个月死亡。
我们对该病例的经验表明,当颅内肿块伴有软脑膜播散时,尤其是当质子磁共振波谱和动态磁敏感对比灌注加权成像提示为恶性肿瘤而扩散加权成像未提示时,应将脑膜黑色素瘤纳入鉴别诊断。并且典型黑色素信号的缺失不应作为排除脑膜黑色素瘤的标准。