| Literature DB >> 30042918 |
Abhishek Lunagariya1, Chintan Rupareliya2, Pradeep C Bollu3, Zabeen Mahuwala2.
Abstract
Giant cell arteritis (GCA) or temporal arteritis (TA) is a granulomatous inflammation of medium to large-sized arteries. It may have a diverse presentation. The most common presenting symptoms of GCA are fever, malaise, unilateral headache, jaw claudication, polymyalgia rheumatica (PMR) and ophthalmoplegia. Most severe sequelae of GCA could be blindness. We report a case of a 65-year-old Caucasian male who presented for the third time with recurrent episodes of diplopia. Neurologic exam showed bilateral cranial nerve (CN) VI palsy, slightly worse on the right than the left side. Other focal neurological deficits were absent. GCA was considered and biopsy of the temporal artery was performed which showed necrotizing pan-arteritis, consistent with GCA. The patient was empirically treated with intravenous (IV) methylprednisolone while awaiting the biopsy results which resulted in the resolution of the symptoms. As far as we know, this is the second case in the literature about the bilateral sixth CN involvement in the background of GCA.Entities:
Keywords: abducens nerve palsy; bilateral abducens nerve palsy; cranial nerve palsy; giant cell arteritis; necrotizing granulomatous disease; panarteritis; polymyalgia rheumatica; sudden blindness; temporal arteritis
Year: 2018 PMID: 30042918 PMCID: PMC6054368 DOI: 10.7759/cureus.2667
Source DB: PubMed Journal: Cureus ISSN: 2168-8184