Abstract

BackgroundLarge Vessel Giant Cell Arteritis (LV GCA) can cause significant narrowing of the subclavian and axillary arteries, either by inflammation or remodelling, which reduces blood pressure in the arms. Also, Raynaud’s phenomenon (RP) has been observed in GCA patients.ObjectivesThis study aims to investigate the presence of Raynaud’s phenomenon in patients with GCA.MethodsPatients diagnosed with GCA were given a validated questionnaire (CSQ)1 on symptoms fitting RP, divided into the different phases of RP (white, blue/purple, and red discoloration provoked by cold exposure) as not every patient exhibits all phases. In total, 30 GCA patients were enrolled in this study. Furthermore, imaging data (PET-CT, MRI, ultrasound (US), or temporal artery biopsy (TAB) of all GCA patients were evaluated.Results30 GCA patients were included, with a mean age of 68,6 (±6,5) years, when diagnosed. 76,7% were female. Of the 30 GCA patients, 12 (40%) reported monophasic discoloration. Of these 12 GCA patients, 2 (6,7%) patients reported bi- or triphasic discoloration. Of the 12 GCA patients with at least monophasic discoloration, 6 patients reported a new onset RP (< 1 year of diagnosis). Imaging data of these 6 patients showed severe Large Vessel GCA (with subclavian and axillary involvement) in all of these patients, without displaying cranial GCA. Of these 6 patients, 1 was examined with US alone, 3 with PET-CT, and 2 had both US and a PET-CT. 3 patients reported that the RP complaints, disappeared during treatment of the GCA, 3 still had complaints. Interestingly all these 3 patients had stenosis of either the subclavian, the axillary artery, or both.ConclusionWe found an increased prevalence of monophasic Raynaud’s phenomenon in GCA patients that is 3,7 times higher, when compared to a local background population2. When looking at new onset RP in GCA, all patients were found positive for Large Vessel GCA, without cranial symptoms. The data of this study warrants a closer look at LV involvement in patients presenting with Raynaud’s phenomenon and GCA or PMR like symptoms.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.