Huang Tsung-Wei, Young Yi-Ho
Department of Otolaryngology, Far Eastern Memorial Hospital, Taipei, Taiwan.
Otol Neurotol. 2002 Nov;23(6):975-9. doi: 10.1097/00129492-200211000-00027.
The possibility of metastasis to the cerebellopontine angle should be considered when a cancer patient has inner ear-related symptoms, although such metastasis is rare. Distinguishing between an independent tumor and a metastasis presents a challenge to the clinician once magnetic resonance imaging reveals a space-occupying lesion in the cerebellopontine angle. This study attempted to differentiate between primary benign and metastatic malignant cerebellopontine angle tumors in cancer patients.
University hospital.
A total of 174 cancer patients with inner ear-related symptoms such as vertigo, hearing loss, or tinnitus were seen at the university hospital from January 1994 to December 2000. All patients underwent a battery of audiologic and neurotologic tests. Magnetic resonance imaging was performed either when the clinical presentation suggested vertigo of central origin or when sensorineural hearing loss developed.
Magnetic resonance imaging confirmed tumors of the cerebellopontine angle in 6 (3%) of the 174 patients, including 3 men and 3 women. Their ages ranged from 46 to 80 years (mean 62 years). The final diagnoses were breast cancer with cerebellopontine angle metastasis (1), breast cancer with cerebellopontine angle epidermoid cyst (1), colon cancer with cerebellopontine angle metastasis (1), colon cancer with acoustic neuroma (1), nasopharyngeal carcinoma with cerebellopontine angle metastasis (1), and nasopharyngeal carcinoma with cerebellopontine angle benign tumor (1).
When a cerebellopontine angle tumor is discovered in a cancer patient, metastatic cancer should be suspected when the tumor presents with deficits of the VIIth and VIIIth cranial nerves of rapid progression or bilateral involvement, or extracranial systemic metastasis. Laboratory examinations such as cytologic study of the cerebrospinal fluid and serologic study can assist in the diagnosis.
癌症患者出现内耳相关症状时,应考虑发生小脑脑桥角转移的可能性,尽管这种转移很罕见。一旦磁共振成像显示小脑脑桥角有占位性病变,区分独立肿瘤和转移瘤对临床医生来说是一项挑战。本研究试图区分癌症患者原发性良性和转移性恶性小脑脑桥角肿瘤。
大学医院。
1994年1月至2000年12月期间,共有174例出现眩晕、听力损失或耳鸣等内耳相关症状的癌症患者在该大学医院就诊。所有患者均接受了一系列听力学和神经耳科学检查。当临床表现提示中枢性眩晕或出现感音神经性听力损失时,进行磁共振成像检查。
174例患者中,6例(3%)经磁共振成像证实存在小脑脑桥角肿瘤,包括3名男性和3名女性。他们的年龄在46岁至80岁之间(平均62岁)。最终诊断为乳腺癌伴小脑脑桥角转移(1例)、乳腺癌伴小脑脑桥角表皮样囊肿(1例)、结肠癌伴小脑脑桥角转移(1例)、结肠癌伴听神经瘤(1例)、鼻咽癌伴小脑脑桥角转移(1例)、鼻咽癌伴小脑脑桥角良性肿瘤(1例)。
癌症患者发现小脑脑桥角肿瘤时,若肿瘤出现快速进展的Ⅶ、Ⅷ脑神经功能缺损或双侧受累,或有颅外系统性转移,则应怀疑为转移性癌症。脑脊液细胞学检查和血清学检查等实验室检查有助于诊断。