Article Text

Download PDFPDF
Giant cell arteritis associated with demyelinating polyradiculoneuropathy
  1. M GARCÍA GASALLA,
  2. M YEBRA BANGO,
  3. J A VARGAS NÚÑEZ,
  4. S MELLOR PITA,
  5. M GARCÍA ALVARADO,
  6. A DE ABAJO ALONSO
  1. G GOIZUETA
  1. Department of Internal Medicine
  2. Clínica Puerta de Hierro
  3. Madrid, Spain
  4. Department of Neurophysiology
  1. Dr M Yebra Bango, Servicio de Medicina Interna I, Clínica Puerta de Hierro, C/ San Martín de Porres No 4, 28035 Madrid, Spain

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Peripheral nerve involvement—mononeuritis,1 mononeuritis multiplex, and polyneuropathies2—has been reported in 14% of patients with giant cell arteritis (GCA).3 ,4 GCA associated with acute inflammatory demyelinating polyneuropathy (AIDP) has exceptionally been described.5 ,6 We report an unusual case of this association.

A 67 year old woman presented with a one month history of difficulty in walking, weakness, and proximal myalgia that worsened progressively. Examination showed proximal weakness and abolition of all deep tendon reflexes; there was no sensory deficit and cranial nerve function was normal. Laboratory tests disclosed normal haematological findings with an erythrocyte sedimentation rate (ESR) of 12 mm/1st h; renal and liver function tests, muscle enzymes, and thyroid stimulating hormone were in the normal range. Serum protein electrophoresis, antinuclear antibodies and rheumatoid factors, and serology for Lyme disease, Q fever, mycoplasma, Venereal Disease Research Laboratory …

View Full Text