Paulus W, Romstöck J, Weidenbecher M, Huk W J, Fahlbusch R
Department of Neuropathology, University of Erlangen Medical School, Germany.
J Neurosurg. 1999 Mar;90(3):555-8. doi: 10.3171/jns.1999.90.3.0555.
Middle ear adenocarcinoma is a very rare, locally invasive neoplasm assumed to arise from the middle ear mucosa. Although endolymphatic sac tumor (aggressive papillary middle ear tumor) and jugulotympanic paraganglioma may show brain invasion, intracranial extension of histologically confirmed middle ear adenocarcinoma has not been previously reported. The authors describe a 53-year-old man who suffered from otalgia and tinnitus for more than 10 years and from neurological deficits for 1 year due to a large temporal bone tumor that invaded the temporal lobe. A combined neurosurgical and otolaryngological resection was performed. Pathological analysis revealed a low-grade adenocarcinoma of a mixed epithelial-neuroendocrine phenotype, which showed a close histological similarity to, and topographical relationship with, middle ear epithelium. The authors conclude that middle ear adenocarcinoma belongs to the spectrum of extracranial tumors that have possible local extension to the brain.
中耳腺癌是一种非常罕见的、具有局部侵袭性的肿瘤,推测起源于中耳黏膜。尽管内淋巴囊肿瘤(侵袭性乳头状中耳肿瘤)和颈静脉鼓室副神经节瘤可能会侵犯脑,但组织学确诊的中耳腺癌颅内扩展此前尚无报道。作者描述了一名53岁男性,因颞骨巨大肿瘤侵犯颞叶,出现耳痛和耳鸣10余年,神经功能缺损1年。进行了神经外科和耳鼻喉科联合切除术。病理分析显示为混合上皮-神经内分泌表型的低级别腺癌,其组织学与中耳上皮相似,且存在局部解剖关系。作者得出结论,中耳腺癌属于可能局部扩展至脑的颅外肿瘤范畴。