BACKGROUND/AIM: Malattia leventinese (ML) is an inherited macular degeneration characterised by the presence of small radial drusen. Despite extensive descriptions of this study of the fundus, angiographic features of ML have been inadequately described. The aim is to describe the indocyanine green angiography (ICG) features observed in ML. METHODS: 10 eyes from five consecutive ML patients (aged 27-44 years) were prospectively included. A complete ophthalmological examination including colour fundus photographs, autofluorescence, fluorescein angiography (FA), and ICG was performed. RESULTS: ICG differentiated two types of drusen. Large round aggregated drusen were consistently hypofluorescent in the early phases and presented as hyperfluorescent spots surrounded by halos of hypofluorescence in the late phases. Conversely, small radial drusen were mostly hyperfluorescent in the early phases with decreased fluorescence in the late phases of the ICG sequence. FA also showed differences in staining between the two types of drusen. CONCLUSIONS: ICG angiography revealed marked differences between the large round and small radial drusen observed in ML. The large central drusen presented with an unusual pustuliform feature on the late phases of the ICG sequence. This distinct feature may be useful in the diagnosis of late stage disease when drusen consolidation could obscure the radial drusen.
BACKGROUND/AIM: Malattia leventinese (ML) is an inherited macular degeneration characterised by the presence of small radial drusen. Despite extensive descriptions of this study of the fundus, angiographic features of ML have been inadequately described. The aim is to describe the indocyanine green angiography (ICG) features observed in ML. METHODS: 10 eyes from five consecutive MLpatients (aged 27-44 years) were prospectively included. A complete ophthalmological examination including colour fundus photographs, autofluorescence, fluorescein angiography (FA), and ICG was performed. RESULTS:ICG differentiated two types of drusen. Large round aggregated drusen were consistently hypofluorescent in the early phases and presented as hyperfluorescent spots surrounded by halos of hypofluorescence in the late phases. Conversely, small radial drusen were mostly hyperfluorescent in the early phases with decreased fluorescence in the late phases of the ICG sequence. FA also showed differences in staining between the two types of drusen. CONCLUSIONS:ICG angiography revealed marked differences between the large round and small radial drusen observed in ML. The large central drusen presented with an unusual pustuliform feature on the late phases of the ICG sequence. This distinct feature may be useful in the diagnosis of late stage disease when drusen consolidation could obscure the radial drusen.
Authors: Marcos A Dantas; Jason S Slakter; Silvana Negrao; Roberto A Fonseca; Tatsushi Kaga; Lawrence A Yannuzzi Journal: Ophthalmology Date: 2002-02 Impact factor: 12.079
Authors: E M Stone; A J Lotery; F L Munier; E Héon; B Piguet; R H Guymer; K Vandenburgh; P Cousin; D Nishimura; R E Swiderski; G Silvestri; D A Mackey; G S Hageman; A C Bird; V C Sheffield; D F Schorderet Journal: Nat Genet Date: 1999-06 Impact factor: 38.330
Authors: Edwin M Stone; Terry A Braun; Stephen R Russell; Markus H Kuehn; Andrew J Lotery; Paula A Moore; Christopher G Eastman; Thomas L Casavant; Val C Sheffield Journal: N Engl J Med Date: 2004-07-22 Impact factor: 91.245
Authors: Stephen R Russell; Raghav R Gupta; James C Folk; Robert F Mullins; Gregory S Hageman Journal: Am J Ophthalmol Date: 2004-05 Impact factor: 5.258