Jessica J Ye, Marc A Bouffard, Earllondra Brooks, Yin P Hung, Eyal Y Kimchi
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引用次数: 0
摘要
背景:大多数巨细胞动脉炎(GCA)患者的眼部表现为视力丧失,但也有少数患者伴有复视和其他颅神经病变。病例研究:这里我们要介绍的病例是一名 84 岁的妇女,她曾有多种癌症病史,因出现复视而入住我院。她被发现右眼(OD)有瞳孔散大、上睑下垂和眼肌麻痹,这与合并 R CNIII/CNVI 神经病变以及炎症标记物高度升高一致。考虑到患者的癌症病史,起初对其进行了各种肿瘤性、副肿瘤性、炎症性和感染性多发性颅神经病病因检查;然而,由于这些检查结果均为阴性,GCA 更有可能成为多发性颅神经病的罕见病因。患者接受了颞动脉活检,病理结果显示与巨细胞动脉炎一致,她接受了类固醇治疗,眼球震颤和上睑下垂最终得到了改善。结论:本病例说明,认识到 GCA 是可能导致多发性颅神经病的罕见病因非常重要,包括颞动脉活检的不可或缺的作用。
Giant Cell Arteritis Presenting With Multiple Cranial Neuropathies - Case Report.
Background: Vision loss accounts for most ophthalmic presentations of giant cell arteritis (GCA), but an important minority of patients present with diplopia and other cranial neuropathies. Case study: Here we present the case of an 84-year-old woman with a prior history of multiple cancers who was admitted to our hospital after developing double vision. She was found to have mydriasis, ptosis, and ophthalmoplegia in the right eye (OD) consistent with a combined R CNIII/CNVI neuropathy, as well as highly elevated inflammatory markers. Given her cancer history, the patient was initially worked up for various neoplastic, paraneoplastic, inflammatory, and infectious causes of multiple cranial neuropathies; however, as these results were negative, GCA became a more likely contender as a possible rare cause of multiple cranial neuropathies. The patient underwent temporal artery biopsy which showed pathology consistent with giant cell arteritis, and she was treated with steroids with eventual improvement in ophthalmoplegia and ptosis. Conclusions: This case illustrates the importance of recognizing GCA as a rare possible cause of multiple cranial neuropathies, including the indispensable role of temporal artery biopsy.