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A 57-year-old obese patient admitted to our ophthalmic department complaining of bilateral sense of eye swelling and mild blurring vision. The anterior segment and pupillary reflex were normal on ophthalmological testing. Likewise, eye movements were preserved and she did not report diplopia in any position of gaze. Dilated fundus examination revealed bilateral hemorrhagic papilledema, pre-retinal hemorrhages in both eyes, dot and blot hemorrhages in the peripheral retina. Visual acuity was 20/20 in both eyes. Routine hematological investigations revealed increased both Von Willebrand factor and ristocetin factor and LAC positivity. The lumbar puncture (LP) showed elevated cerebrospinal fluid (CSF) proteins. Magnetic resonance imaging (MRI) with contrast of brain and spinal cord showed signs of intracranial hypertension and the presence of two lesions in continuity with each other respectively located at T12-L1 and L1-L2. Radiologic features were compatible with the diagnosis of ependymoma. A surgical procedure was conducted and confirmed the diagnosis after anatomical pathology analysis.
A-60-year-old female patient without remarkable ocular and/ or systemic history referred for a routine eye examination. Best corrected visual acuties were 20/25 in both eyes. SD-OCT scan cutting through the center revealed lack of foveal pit. In OCT-A slabs, FAZ was not appreciated at superficial and deep capillary plexus levels. She was diagnosed as isolated foveal hypoplasia.
View imageCentral Retinal Artery Occlusion with Hypertensive Retinopathy
View imageWe report the case of an uncomplicated choroidal osteoma in a 27-year-old woman, with no medical history, presented to our department with sudden onset visual loss in her right eye (RE). Opthalmological evaluation revealed a best corrected visual acuity of 4/10 and normal anterior segment in the RE. Fundus examination revealed a slightly elevated, round shaped, yellowish-orange coloured lesion. Choroidal osteoma is a rare and benign ossifying tumor, affecting mostly Caucasian females, in early twenties. This affection is often unilateral, occurring in an apparently healthy eye. It is generally located in juxta or peri-papillary areas. Diagnosis is based on clinical examination, aided by multimodal imaging, including optical coherence tomography (OCT), OCT-angiography and ultrasonography. Choroidal neovascularisation represents its main complication.
A case of an immunocompromised 30-year-old woman with bilateral Candida albicans chorioretinitis. (A) In the right eye structural OCT shows a highly reflective lesion involving the full-thickness retina and protruding into the vitreous. The hyperreflective dots in the posterior vitreous are infiltrating inflammatory cell. (B) In the left eye structural OCT shows two juxtapapillary lesions originating at the retinal pigment epithelium/choroid layer and penetrating into the neurosensory retina. Subretinal fluid is present. The hyperreflective dots in the posterior vitreous are infiltrating inflammatory cell.
View imageA case of 49 y.o. man, caucasian, with no history of drugs and systemic disease, referred to our emergency room due to a sudden para central scotoma in his left eye. Our multimodal imaging allowed us to diagnose a syphilitic posterior placoid chorioretinitis, confirmed few days later with serological exams (qualitative TPHA +).
View imageA case of 24-year-old woman with MEWDS. Structural OCT shows the loss or damage of the outer photoreceptor segments (white arrows). Hypocyanescence of the ICGA is present in the intermediate angiographic phase and most clearly detected in the late phase.
View imageMetallic Intraocular Foreign Body with surrounding retinal hemorrhages and vitreitis. Fundus fotograph (Zeiss), structural OCT (Heidelberg)
View image21 yo female with sickle cell anemia. Panoramic angiography shows areas of diffuse extravasation by neovessels in the retinal periphery, in addition to areas of hypoperfusion compatible with ischemia. DEVICE: California (Optos).
View imageImaging device: A. Color fundus photography, angle 89°, Nidek, B. retromode
View imageDescription: 45 Y/O male with proliferative diabetic retinopathy treated with laser. A retinal neovessel (blue arrow), Intraretinal Microvascular Abnormality (IrMA) (yellow arrow) are evident
Imaging device: Ultrawidefield color fundus photograph 163°, Nidek
Imaging device: A.Color fundus photography, angle 89°, Nidek; B. Structural OCT
View imageImaging device: Ultrawidefield color fundus photograph 163°, Nidek
View imageImaging device: Ultrawidefield color fundus photograph 163°, Nidek
View imageImaging device: A. Color fundus photography, angle 89°, Nidek; B. fundus autofluorescence; C. retromode DL; D. rretromode DR; E. structural OCT
View imageImaging device: Color fundus photography, angle 89°, Nidek
View imageImaging device: Color fundus photography, angle 89°, Nidek
View imageImaging device: Ultrawidefield color fundus photograph 163°, Nidek
View imageImaging device: Color fundus photography, angle 89°, Nidek
View imageImaging device: Color fundus photography, angle 89°, Nidek
View image78 yo female with RPE tear. DEVICE: Fundus fotograph (Zeiss), structural OCT (Heidelberg)
View image34 yo female with atrophic maculopathy and adjacent flecks. DEVICE: Color fundus photograph (Tocpon)
View image25 y/o male with visual reduction showing macular schisi with detachment due to optic coloboma.
A. Color fundus photograph
B. Structural OCT showing the retina splitted at both the inner and outer retinal layers with a macular detachment
DEVICE: Fundus photograph (Topcon), Structural OCT (Topcon)
A. Fundus photograph showing vast round placoid yellow zone in the posterior pole;
B. FA reveals hyperfluorescence of the optic disk with a zone of hyperfluorescence in the posterior pole (tissue staining).
C. Structural OCT shows disruption of the ellipsoid zone and hyperreflective, nodular thickening of the RPE. Hyperreflective dots representing inflammatory cells are visible in the vitreous and attached to the posterior hyaloid.
DEVICE: Multimodal imaging: fundus photograph, FA, Structural OCT
37 Y/O male with an eccentric yellow lesion (orange arrow) corresponding to a neurosensory retinal detachment. DEVICE: Fundus camera, Zeiss.
View imageColor fundus photograph (A) 45 Y/O female with serpiginoid lesion extending from the juxtapapillary area. Intermediate-phase fluorescein angiogram photographs (B) of the same eyes delineating the typical hyperfluorescent margins of the serpiginoid lesions. Fundus autofluorescence image (C) of the same eye, disclosing predominantly hyperautofluorescent lesion with stippled hypoautofluorescence delimited by a thin rim of hypoautofluorescence. DEVICE: Multimodal imaging: (A) Color fundus photograph (Zeiss), (B) FA (Heidelberg), (C) Fundus autofluorescence (Heidelberg).
View image45 Y/O female with serpiginoid lesion extending from the juxtapapillary area. DEVICE: Fundus Camera, Zeiss
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