Literature DB >> 16619815

[Multifocal choroiditis and panuveitis (MCP)--diagnosis, ocular symptoms and treatment].

Joanna Brydak-Godowska1, Marcin Swituła, Ewa Dróbecka-Brydak, Marzena Mzyk, Elzbieta Sedrowicz, Agnieszka Samsel.   

Abstract

Multifocal choroiditis and panuveitis (MCP) belong to white dot syndromes, which are an idiopathic inflammatory process damaging the retinal pigment epithelium and choriocapillaris. We observed fourteen patients with typical ocular changes for MCP (panuveitis with typical multiple yellow, white or gray focal lesions in fundus of the eye). In 8 patients typically were observed--glaucoma, cataract, macular edema. We applied topical drops (corticosteroids, antiglaucomatous), and in 5 patients oral encorton was necessary to include.

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Year:  2005        PMID: 16619815

Source DB:  PubMed          Journal:  Klin Oczna        ISSN: 0023-2157


  2 in total

1.  White dot syndromes: a 20-year study of incidence, clinical features, and outcomes.

Authors:  Nakhleh E Abu-Yaghi; Stella P Hartono; David O Hodge; Jose S Pulido; Sophie J Bakri
Journal:  Ocul Immunol Inflamm       Date:  2011-12       Impact factor: 3.070

2.  Observation and Clinical Pattern in Patients with White Dot Syndromes: The Role of Color Photography in Monitoring Ocular Changes in Long-Term Observation.

Authors:  Joanna Brydak-Godowska; Joanna Gołębiewska; Monika Turczyńska; Joanna Moneta-Wielgoś; Agnieszka Samsel; Piotr K Borkowski; Michał Ciszek; Agnieszka Płonecka-Rodzoch; Aleksandra Kużnik-Borkowska; Joanna Ciszewska; Elżbieta Makomaska-Szaroszyk; Lidia B Brydak; Dariusz Kęcik
Journal:  Med Sci Monit       Date:  2017-03-02
  2 in total

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