June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Ocular manifestations of Granulomatosis with Polyangiitis from the “Institute of Ophthalmology Conde de Valenciana”
Author Affiliations & Notes
  • Miguel Pedroza-Seres
    Dept of Uveitis & Ocular Immunol, Institute of Ophthalmology, Mexico City, Mexico
  • Edson Robles
    Dept of Uveitis & Ocular Immunol, Institute of Ophthalmology, Mexico City, Mexico
  • Diana González
    Dept of Uveitis & Ocular Immunol, Institute of Ophthalmology, Mexico City, Mexico
  • Footnotes
    Commercial Relationships Miguel Pedroza-Seres, None; Edson Robles, None; Diana González, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 2912. doi:
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      Miguel Pedroza-Seres, Edson Robles, Diana González; Ocular manifestations of Granulomatosis with Polyangiitis from the “Institute of Ophthalmology Conde de Valenciana”. Invest. Ophthalmol. Vis. Sci. 2013;54(15):2912.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To describe the main clinical ocular manifestations and the immunosuppressive medication used in Granulomatosis with Polyangiitis in a tertiary eye care center (Insitute of Ophthalmology Conde de Valenciana).

Methods: Medical records of Granulomatosis with Polyangiitis patients were compiled and reviewed from September 2007 until August 2012. A database was made combining all the ocular clinical manifestations listed. Percentage of occurrence for each ocular disease as a first manifestation in Granulomatosis with Polyangeiitis were obtained and categorized. The immunosuppressive treatment was reviewed too.

Results: Among the 34 patients identified, 53% have uniocular disease and 47 % have binocular disease. Anterior diffuse scleritis was the most frequent ocular manifestation affecting 32% of the population. Necrotizing scleritis was presented in 29% of the patients. PUK was the first manifestation in 15% of our population. Orbital disease appeared in 9%. Nodular scleritis were identified in 6%. Retinal vasculitis was infrequent affecting only 3% also anterior uveitis (3%). The main medication administered were oral cyclophosphamide and oral methotrexate in 41% of the patients each one, intravenous cyclophosphamide and azathioprine were used in 26.5%. Mycophenolate mofetilo was used in 6%. Only one patient was taking Anti TNF drugs.

Conclusions: The main ocular manifestation of Granulomatosis with Polyangiitis in our hospital was scleritis and the most common treatment used was oral cyclophosphamide and oral mthotrexate.

Keywords: 745 uvea • 557 inflammation • 459 clinical (human) or epidemiologic studies: biostatistics/epidemiology methodology  
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