Fundus autofluorescence imaging in hereditary ATTR amyloidosis with ocular involvement

被引:8
|
作者
Veronese, Chiara [1 ]
Marcheggiani, Eleonora B. [1 ]
Tassi, Filippo [1 ]
Gallelli, Ilaria [2 ]
Armstrong, Grayson W. [3 ]
Ciardella, Antonio P. [1 ]
机构
[1] Univ Bologna, S Orsola M Malpighi Hosp, Ophthalmol Unit, I-40138 Bologna, Italy
[2] Univ Bologna, S Orsola M Malpighi Hosp, Inst Cardiol, I-40138 Bologna, Italy
[3] Brown Univ, Warren Alpert Med Sch, Div Ophthalmol, Providence, RI 02912 USA
来源
关键词
Familial amyloid polyneuropathy; Glu54Lys; hyper-autofluorescence; transthyretin; vitreous floaters; POLYNEUROPATHY;
D O I
10.3109/13506129.2013.823082
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fundus autofluorescence (AF) is a non-invasive technique for the evaluation of intrinsic autofluorescence of the tissues within the eye. In recent years, autofluorescence has become an important diagnostic tool for the assessment of various ocular diseases. A previous study has found that ex vivo Ab amyloid plaques in the retina of a transgenic mouse model appear hyper-autofluorescent (hyper-AF) under specific wavelengths (excitation at 830 nm, emission at 630). We report the first description of hyper-AF ocular findings in a case of transthyretin-related familial amyloid polyneuropathy (FAP) associated with ocular involvement using AF imaging. A 47-year-old woman from Italy presented to our institution with a history of early onset FAP with ocular involvement due to the rare amyloidogenic transthyretin Glu54Lys mutation. AF imaging showed hyper-AF amyloid deposits associated with retinal vessels in both eyes and a hyper-AF amyloid deposit anterior to the optic disk in the right eye. Conclusion and Relevance: Further studies in FAP patients with different types of genetic mutations and various disease-stages are needed to better establish if non-invasive AF imaging is useful in detecting ocular amyloidosis.
引用
收藏
页码:269 / 271
页数:3
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