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Multifocal Vitelliform Retinal Lesion


Authors: T. Streicher 1;  J. Špirková 1;  M. Ilavská 2
Authors‘ workplace: Očné oddelenie NsP Bojnice, primárka MUDr. Ida Simonidesová 1;  Očná ambulancia NsP sv. Lukáša Galanta, vedúca lekárka MUDr. Monika Ilavská, PhD 2
Published in: Čes. a slov. Oftal., 71, 2015, No. 3, p. 175-178
Category: Case Report

Overview

The authors present retrospective follow up of patient with bilateral multifocal vitelliform retinal lesion during the 18 years period. At this time, spontaneous improvement of objective picture on retina and subjective visual troubles was observed. It is probable, that this case is a part of the same symptom complex as a variant of Best´s hereditary disease. This conclusion was based on initial stadium of phenotypical expressivity and additional evaluations. The course and outcomes of visual functions were different. The hereditary transmission was not confirmed.

Key words:
multifocal vitelliform retinal lesion, electrophysiology of retina, the fluorescence angiography, optical coherence tomography


Sources

1. Boon, C.J., Klevering, B.J., den Hollander, A.I. et al.: Clinical and genetic heterogeneity in multifocal vitelliform dystrophy. Arch Ophthalmol, 125; 2007: 1100–1106.

2. Conrads, H., Bichmann, W.: Multiple vitelliforme Netzhautzysten. Klin.Mbl.Augenheilk, 182; 1983. 241–243.

3. Denden, A: Über wenig bekannte multiple vitelliforme Retinalzysten des hinteren Fundusabschnittes. Klin Mbl Augenheilk, 149; 1966: 609–626.

4. Denden, A., Littann, K.E.: Über die Spätform der multiplen vitelliformen Netzhautzysten. Ophthalmologica, 164; 1972: 84-96.

5. Deutman, A.F.: The hereditary dystrophies of the posterior pole of the eye. Van Gorcum, Assen 1971; p. 198–299.

6. Jarc-Vidmar, M., Kraut, A., Hawlina, M: Fundus autofluorescence imaging in Best´s vitelliform dystrophy. Klin Mbl Augenheilk, 220; 2003: 861–867.

7. Hittner, H.M., Ferrell, R.E., Borda, R.P. et al.: Atypical vitelliform macular dystrophy in a 5-generation family. Br J Ophthalmol, 68; 1984: 199–207.

8. Laloum, J.E., Deutman, A.F.: Lésions vitelliformes périphériques dans une dystrophie vitelliforme de la macula. J Fr Ophtalmol, 14; 1991: 74–78.

9. Lisch,W., Weidle, E.G., Richard, G. et al.: Multiple vitelliforme Netzhautzysten. Klin.Mbl.Augenheilk, 194; 1989: 120–128.

10. Littann, K.E.: Multiple vitelliforme Netzhautzysten. Ber. dtsch.ophthalmol. Ges.München, Bergmann, 1965: 442–445.

11. Loewenstein,A., Godel,V., Godel,L. et al.: Variable phenotypic expresivity of Best´s vitelliform dystrophy. Ophthamic Paediatrics and Genetics, 14; 1993: 131–136.

12. Miller,S.A.: Multifocal Best´s vitelliform dystrophy. Arch Ophthalmol, 95; 1977: 984–990.

13. Mullins,R.F., Oh,K.T., Heffron,E. et al.: Late development of vitelliform lesions and flecks in a patient with Best disease. Arch.Ophthalmol., 123; 2005: 1588–1594.

14. Pece,A., Gaspari,G., Avanza,P. et al.: Best´s multiple vitelliform degeneration. Int.Ophthalmol., 16; 1992: 459-464.

15. Remky,H., Kölbl,I.: Multiple vitelliforme Zysten. Klin. Mbl. Augenheilk., 159; 1971: 322-329.

16. Renner,A.B., Tillack,H., Kraus,H.et al.: Late onset is common in Best macular dystrophy associated with VMD2 gene mutations. Ophthalmology, 112; 2005: 586–592.

17. Sorr,E.M., Goldberg,R.E.: Vitelliform dystrophy in a 64-year-old man. Am J Ophthalmol, 82; 1976: 256–258.

18. Streicher, T., Špirková, J., Tichá, M: Klinická rozmanitosť Bestovej choroby. Čes a Slov Oftal, 68; 2012: 189–194.

19. Walter, P., Brunner, R., Heimann, K.: Atypical presentations of Best´s vitelliform macular degeneration: clinical finding in seven cases. German J. Ophthalmology, 3; 1994: 440–444.

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