Arteritis de células gigantes: ¿Cómo debutan pacientes chilenos?. Análisis de casos y revisión de la literatura.

Resumen

Background: Giant cell Arteritis (GCA) is the most common systemic vasculitis in patients over 50 years. Diagnosis is based on clinical, laboratory, imaging, and biopsy. Temporal artery biopsy (TAB) may be inconclusive in up to 40% of patients. Aim: To describe disease features of patients diagnosed with GCA. Material and Methods: Review of pathology reports of giant cell arteritis and clinical records of patients seen with the diagnosis between 2000 and 2019. Demographic, clinical, laboratory, histopathology, imaging, treatment, and follow-up variables were analyzed. Results: We fetched 32 patients with a median age at diagnosis of 70.5 years (range 57-90), 81% women. Twenty eight percent had polymyalgia. 72% had only cranial symptoms, 12% had extracranial involvement and 13% exclusive extracranial involvement. The median time from onset of symptoms to diagnosis was two months (range 0.5-8). All had elevated erythrocyte sedimentation rate and c reactive protein. A TAB was performed in 27 patients and in 17 (65.4%) it confirmed the diagnosis. Transmural inflammation was the most frequent finding. All patients received steroids. Follow-up information was available from 25 patients and 92% received a steroid-sparing agent, usually methotrexate (74%). Ninety two percent achieved clinical remission in the first year and 59% had minor relapses during steroid tapering. Conclusions: Our patients showed frequent extracranial involvement and TAB was a useful diagnostic tool.