Capobianco David J, Brazis Paul W, Rubino Frank A, Dalton Jon N
Department of Neurology, Mayo Clinic, Jacksonville, Fla 32224, USA.
Headache. 2002 Feb;42(2):142-6. doi: 10.1046/j.1526-4610.2002.02032.x.
Review the clinical features of occipital condyle syndrome.
Occipital condyle syndrome consists of unilateral occipital region pain associated with ipsilateral 12th cranial nerve paresis. It is typically due to metastasis to the skull base and is underdiagnosed.
We report a retrospective case series of 11 patients (8 men, 3 women), aged 32 to 72 years.
Eleven cases of occipital condyle syndrome were identified. All patients complained of severe occipital region pain. In addition, 2 patients complained of ipsilateral ear or mastoid pain, 2 noted associated vertex pain, and 2 had frontal region pain. Six of the 11 cases involved the right side. In all patients, the occipital pain was ipsilateral to the 12th nerve paresis. All patients were mildly dysarthric, and 3 had dysphagia. In 7 of the 11 patients, occipital region pain preceded the hypoglossal paresis by several days to 10 weeks. On examination, tenderness to palpation of the occipital region was noted in all patients. All 11 patients had unilateral hypoglossal paresis. Skull films were abnormal in 2 of 5 patients for whom they were obtained, and tomograms were abnormal in 1 of 2 patients. High-quality computed tomography, bone scanning, and magnetic resonance imaging were abnormal in all cases in which they were performed. Nine patients had a known primary malignancy. The most common malignancies were breast cancer in women (2 of 3) and prostate cancer in men (4 of 8). In 2 patients, occipital condyle syndrome was the initial manifestation of a metastatic lesion. Radiation therapy was the treatment of choice for the occipital region pain.
Occipital condyle syndrome is a rare, but stereotypic syndrome. Early detection has important therapeutic implications. Evaluation of the craniovertebral junction with special attention to the occipital condyles should be a routine part of all brain and cervical spine radiologic examinations, and the possibility of occipital condyle syndrome, particularly when patients have persistent occipital pain and a history of cancer, should be considered.
回顾枕髁综合征的临床特征。
枕髁综合征表现为单侧枕部疼痛并伴有同侧第12对脑神经麻痹。它通常是由颅底转移瘤引起的,且诊断不足。
我们报告了一组11例患者(8例男性,3例女性)的回顾性病例系列,年龄在32至72岁之间。
确诊11例枕髁综合征。所有患者均主诉枕部剧痛。此外,2例患者主诉同侧耳部或乳突疼痛,2例伴有头顶疼痛,2例有额部疼痛。11例中有6例累及右侧。所有患者枕部疼痛均与第12对脑神经麻痹同侧。所有患者均有轻度构音障碍,3例有吞咽困难。11例患者中有7例枕部疼痛先于舌下神经麻痹数天至10周出现。检查时,所有患者枕部触诊均有压痛。11例患者均有单侧舌下神经麻痹。5例患者行颅骨平片检查,2例异常;2例患者行断层扫描,1例异常。所有行高质量计算机断层扫描、骨扫描和磁共振成像检查的病例均异常。9例患者有已知的原发性恶性肿瘤。最常见的恶性肿瘤在女性为乳腺癌(3例中的2例),在男性为前列腺癌(8例中的4例)。2例患者中,枕髁综合征是转移瘤的首发表现。放射治疗是枕部疼痛的首选治疗方法。
枕髁综合征是一种罕见但具有典型特征的综合征。早期发现具有重要的治疗意义。对颅颈交界区进行评估,尤其关注枕髁,应成为所有脑部和颈椎放射学检查的常规部分,并且应考虑枕髁综合征的可能性,特别是当患者有持续性枕部疼痛且有癌症病史时。