Burton E A, Winer J B, Barber P C
University of Oxford, Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QU, UK.
J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):223-6. doi: 10.1136/jnnp.67.2.223.
The clinical and histopathological details of a patient who succumbed to giant cell arteritis (GCA) of the cervical radicular vessels are described. The initial clinical presentation, with diaphragmatic weakness, has not previously been reported. Normal inflammatory indices and the unusual presentation prevented diagnosis during life, but GCA should be considered in the differential diagnosis of any unexplained neuropathic or radiculopathic syndrome, as corticosteroid therapy may lead to recovery. This is the first account of the pathological findings in cervical radiculopathy associated with GCA.
本文描述了一名死于颈神经根血管巨细胞动脉炎(GCA)患者的临床和组织病理学细节。最初的临床表现为膈肌无力,此前未见报道。正常的炎症指标和不寻常的表现导致生前未能确诊,但在任何不明原因的神经病变或神经根病变综合征的鉴别诊断中都应考虑GCA,因为皮质类固醇治疗可能会使病情恢复。这是关于与GCA相关的颈神经根病病理发现的首次报道。