Chang Patrick C, Fischbein Nancy J, McCalmont Timothy H, Kashani-Sabet Mohammed, Zettersten Elizabeth M, Liu Amon Y, Weissman Jane L
Department of Radiology, University of California, San Francisco, School of Medicine, San Francisco, CA 94143, USA.
AJNR Am J Neuroradiol. 2004 Jan;25(1):5-11.
Extension of malignant melanoma along cranial nerves is a little-known complication of malignant melanoma of the head and neck. We describe the clinical and MR imaging findings of perineural spread of malignant melanoma to cranial nerves, emphasizing that this entity occurs more commonly with desmoplastic histology and may have a long latent period following primary diagnosis.
At two institutions, we identified and retrospectively reviewed eight cases of malignant melanoma of the head and neck that had MR imaging evidence of perineural spread of disease. All patients underwent confirmatory tissue sampling.
Seven patients had melanomas of the facial skin or lip, and one patient had a primary sinonasal lesion. By histopathology, these melanomas included five desmoplastic, two mucosal, and one poorly differentiated melanotic spindle-cell tumor. All patients developed symptomatic cranial neuropathy an average of 4.9 years from the time of initial diagnosis. MR imaging demonstrated postgadolinium enhancement of at least one branch of the trigeminal nerve in all cases and of at least one other cranial nerve in five cases. Other findings included abnormal contrast enhancement and soft tissue thickening in the cavernous sinus, Meckel's cave, and/or the cisternal segment of the trigeminal nerve.
Although perineural spread of disease occurs most commonly with squamous cell carcinoma and adenoid cystic carcinoma, malignant melanoma must also be included in this differential diagnosis, particularly if the patient's pathology is known to be desmoplastic. Similarly, any patient with malignant melanoma of the head and neck who undergoes MR imaging should receive an imaging assessment focused on the likely routes of perineural spread.
恶性黑色素瘤沿颅神经蔓延是头颈部恶性黑色素瘤一种鲜为人知的并发症。我们描述了恶性黑色素瘤向颅神经周围神经蔓延的临床及磁共振成像(MR)表现,强调该情况在促纤维增生性组织学类型中更常见,且在初次诊断后可能有较长的潜伏期。
在两家机构,我们识别并回顾性分析了8例头颈部恶性黑色素瘤患者,这些患者有疾病周围神经蔓延的MR成像证据。所有患者均接受了确诊性组织取样。
7例患者的黑色素瘤位于面部皮肤或唇部,1例患者原发于鼻窦。经组织病理学检查,这些黑色素瘤包括5例促纤维增生性、2例黏膜性和1例低分化黑色素性梭形细胞瘤。所有患者在初次诊断后平均4.9年出现有症状的颅神经病变。MR成像显示所有病例中三叉神经至少一个分支在注射钆对比剂后强化,5例中至少有一条其他颅神经强化。其他表现包括海绵窦、梅克尔腔和/或三叉神经脑池段对比增强异常及软组织增厚。
尽管疾病周围神经蔓延最常见于鳞状细胞癌和腺样囊性癌,但在鉴别诊断中也必须考虑恶性黑色素瘤,特别是已知患者病理类型为促纤维增生性时。同样,任何接受MR成像检查的头颈部恶性黑色素瘤患者都应接受针对周围神经蔓延可能途径的成像评估。