Department of Otolaryngology-Head and Neck Surgery, Eastern Virginia Medical School, Norfolk, Virginia.
Otol Neurotol. 2021 Dec 1;42(10):e1560-e1564. doi: 10.1097/MAO.0000000000003293.
We report disease remission and recovery of fifth and seventh nerve paresis in a case of primary mucosal melanoma of the middle ear and petrous temporal bone.
A 74-year-old man developed sudden, profound, right sided sensorineural hearing loss, disequilibrium, otalgia, and cranial nerve V and VII dysfunction. Imaging demonstrated an unresectable, osteolytic lesion involving the middle ear and anterior petrous apex. Melanoma was diagnosed via in-office biopsy; whole-body metabolic imaging revealed no other primary site.
Multidisciplinary management included radiation therapy (30 Gy, 10 fractions) followed by induction (five cycles, q2w) and maintenance nivolumab (six cycles, q3w).
Complete metabolic response of primary site and metastases on imaging, recovery of cranial neuropathies.
Following palliative radiation therapy and induction nivolumab, cranial neuropathies resolved. With maintenance-dose nivolumab, primary site and metastases exhibited a complete response. Therapy was stopped at 16 months post-diagnosis. Complete remission was maintained until 22 months after diagnosis. The patient developed a solitary cerebral metastasis which was refractory to radiosurgery and biopsy confirmed melanoma. He expired 2 years, 8 months post-diagnosis.
Mucosal melanoma of the middle ear and petrous temporal bone is exceedingly rare. Management is individualized and surgery is undertaken when possible. Key observations in this case are the complete metabolic response and reversal of cranial nerve neuropathies following radiation and anti-programed cell death receptor ligand 1 therapy. Non-surgical treatment is worthy of study as initial management for similar lesions.
我们报告了一例中耳和颞骨岩部原发性黏膜黑色素瘤病例中第五和第七脑神经麻痹的缓解和恢复。
一名 74 岁男性突发严重右侧感音神经性听力损失、失衡、耳痛和第五和第七脑神经功能障碍。影像学显示无法切除的中耳和前岩尖溶骨性病变。通过门诊活检诊断为黑色素瘤;全身代谢成像未发现其他原发性部位。
多学科管理包括放射治疗(30Gy,10 个剂量),随后进行诱导(五个周期,每两周一次)和维持纳武单抗(六个周期,每三周一次)。
原发性和转移灶的代谢完全缓解,颅神经麻痹的恢复。
姑息性放射治疗和诱导纳武单抗治疗后,颅神经麻痹得到缓解。维持剂量纳武单抗治疗后,原发性和转移灶完全缓解。在诊断后 16 个月停止治疗。诊断后 22 个月完全缓解仍维持。患者出现孤立性脑转移,对放射外科治疗有抗性,活检证实为黑色素瘤。他在诊断后 2 年 8 个月去世。
中耳和颞骨岩部黏膜黑色素瘤极为罕见。治疗是个体化的,在可能的情况下进行手术。该病例的关键观察结果是放射治疗和抗程序性细胞死亡受体配体 1 治疗后代谢完全缓解和颅神经病变的逆转。非手术治疗作为类似病变的初始治疗值得研究。