ABSTRACT
This case report of a 38-year-old man with bilateral Best vitelliform macular dystrophy (BVMD) presents bilateral quiescent type 1 neovascularizations (NV) detected by optical coherence angiography (OCTA) and their multimodal imaging characteristics. It was emphasized that this kind of quiescent and asymptomatic NV may be present in nearly every stage of BVMD and it was concluded that OCTA is a noninvasive, easy, and rapid method that is superior to other imaging methods in detecting them.
Introduction
Best vitelliform macular dystrophy (BVMD), or Best disease, is a bilateral hereditary disease that has autosomal dominant inheritance and is characterized by a typical “egg-yolk” appearance in the macula. The disease emerges in childhood and young adulthood and has 5 stages based on clinical appearance.1,2 It generally progresses slowly, with a decrease in visual acuity that is minimal and inconsistent with the fundus appearance in the early stages. There is often asymmetry in visual acuity between the eyes, and central scotomas and metamorphopsia appear at later stages.3,4
Reports indicate that sudden vision loss during the natural course of BVMD is caused by secondary neovascularization (NV) and is a relatively common occurrence.3,4,5,6,7 Optical coherence tomography angiography (OCTA) is a fairly new, rapid, and noninvasive imaging method currently used to investigate the presence of all types of NV and polypoidal choroidal vasculopathy (PCV) in the retinal and choroidal layers. In addition, it has been reported in various studies that OCTA may be useful in various retinal diseases for the early detection of inactive and quiescent NV structures that do not yet show exudative symptoms.8
To the best of our knowledge, this article is the first to present asymptomatic and quiescent type 1 NV lesions detected by OCTA and their multimodal imaging features in both eyes of a patient diagnosed with bilateral BVMD.
Discussion
In this article, we present asymptomatic and quiescent type 1 NV lesions detected only by OCTA in both eyes of a patient diagnosed with bilateral BVMD and their characteristics on multimodal imaging with OCTA as well as color and infrared photography, FAF, SD-OCT, FA, and ICGA. To the best of our knowledge, this article is the first to describe asymptomatic and quiescent type 1 NV and its multimodal imaging features in a patient with BVMD.
Several studies published in recent years have reported that quiescent NV lesions can be found in many retinal diseases, especially age-related macular degeneration, and that they may remain asymptomatic for years.8,9 Histologically, NVs are divided into three types: type 1 NV, which is located under the retinal pigment epithelium (RPE) (angiographically occult); type 2, which originates from the choroid and passes through Bruch’s membrane and RPE to extend into the subretinal space (angiographically classic); and type 3, which develops within the neurosensory retina (retinal angiomatous proliferation).10 In our case, the NV lesion was seen at the choriocapillaris level on OCTA and was therefore classified as type 1. NV lesions in both eyes were considered inactive (quiescent) due to the absence of macular hemorrhage on clinical examination, no findings of subretinal, intraretinal, or sub-RPE fluid on SD-OCT, and no leakage in late FA.11,12 The absence of fibrosis on clinical examination and imaging ruled out the possibility of scar tissue. The fact that the patient’s eyes had very similar visual acuity, as well as being compatible with stage 3 and 4 BVMD and the patient having no complaints of a sudden decrease in vision also suggested that the NV was asymptomatic.
Using OCTA, Batıoğlu et al.3 detected NV networks with associated polypoidal dilations at the choriocapillaris level in both eyes of a pregnant BVMD patient with complaints of reduced vision, and described the case as pachychoroid neovasculopathy. In our patient, a nodular formation was detected just below the macular center in the left eye and resembled a pointed PED on SD-OCT. We thought that it may be associated with a polypoidal structure and performed ICGA, but this diagnosis was discounted because its staining properties on ICGA were not typical for PCV.
There are many articles in the literature describing secondary NV lesions and their OCTA imaging features in eyes with BVMD. Patel et al.5 used OCTA to examine eyes with 4 different retinal dystrophies and secondary NV development and emphasized that the morphological structure of the NV lesions could be clearly demonstrated on OCTA despite distortion of the retinal anatomy. Shahzad and Siddiqui6 were able to visualize type 2 NV lesions secondary to BVMD with OCTA in one eye of a pediatric patient presenting with a sudden decline in vision. Guduru et al.4 examined the vascular structure of the retina with OCTA and FA in 19 eyes with secondary NV. They reported that OCTA was superior to FA in measuring NV and that the ring-shaped NV pattern was rare. Stattin et al.7 presented the features of multimodal imaging using FAF, SD-OCT, FA, ICGA, and OCTA in a BVMD patient with metamorphopsia and sudden decline in vision in one eye. Researchers have detected NV lesions at the outer retinal and choriocapillary levels with OCTA while emphasizing that conventional angiography techniques such as FA and ICGA were inconclusive. In our case, we were only able to visualize the presence of a quiescent type 1 NV lesion at the choriocapillary level in both eyes with OCTA.
In summary, we concluded that OCTA is a noninvasive, easy, rapid, and reliable imaging method superior to other modalities for detecting secondary NV lesions in eyes with BVMD, even if quiescent and asymptomatic.
