von Hippel-Lindau (VHL) (MIM#193300) disease is an autosomal dominant inherited disorder that is classically associated with benign or malignant tumors in multiple organs. The most frequent tumors are retinal hemangioblastoma (RH) and central nervous system (CNS) hemangioblastomas, renal cell carcinoma (RCC), pheochromocytoma, pancreatic islet cell tumors and endolymphatic sac tumours [1]. von Hippel-Lindau disease most commonly presents between the ages of 25 and 40, and the prevalence of the disease is 1 in 35000 [2]. Retinal hemangioblastoma is the most frequent neoplasm and the most common clinical sign of the disease; it is seen in 40.0-60.0% of patients [1]. Retinal hemangioblastomas are benign tumors that may be localized peripherally or juxtapapillary and show a slow-growing pattern [3].
In 1993, mutational inactivation of tumor suppressor genes in chromosome 3p25-p26 were found to be responsible for VHL [4]. The VHL coding sequence is represented in three exons and encodes two VHL proteins[5]. The
On ophthalmological examination, best-corrected visual acuity (BCVA) was counting fingers from 2 meters in the right eye and 1.0 in the left eye on the Snellen acuity visual chart. Vitritis was detected in the right eye on slit-lamp biomicroscopy. The fundus examination revealed an extensive lipid exudation on the fovea and macula, and a 3-4 optic disc diameter-sized RH at the equator in the right eye; it was normal in the lefteye. Fundus fluorescein angiography (FFA) showed that the RH in the right eye was responsible for fluorescein staining on the feeding artery and drainage vein and fluorescein leakage. Optical coherence tomography (OCT) showed that there was a foveal detachment in the right eye (Figure 2).
The patient’s blood sample was collected in vacutainers containing EDTA as anticoagulant. After DNA extraction (EZ1 Advanced Instruments; Qiagen, Hilden, Germany), mutation analysis of the
A heterozygous missense mutation c.202T>C, (p.Ser 68Pro) in exon 1 of the
The pathogenicity of the variation was tested in the Polyphen database and it was scored as probably damaging [probably damaging with a score of 0.960 (sensitivity: 0.78; specificity: 0.95)]. However, this variation was not listed the in the Exac database.
Best-corrected visual acuity was 1.0 on the Snellen acuity chart in the right eye and no light perception in the left eye. Biomicroscopic examination was normal in both eyes. The fundus examination revealed optic nerve atrophy and two RH at the equator in the left eye, and was normal in the right eye. Fundus fluorescein angiography showed that hyperfluorescence and fluorescein leakage was caused by the lesions. Hyper reflectance was observed under the cross-section of the RH, and the macular section was normal in OCT (Figure 6). The same mutation as in Case 1 was also detected in the genetic analysis (c.202T>C, p.Ser 68Pro).
Fundus fluorescein angiography is the most informative diagnostic method because of the vascular nature of a RH. Fluorescein is apparent in the dilated feeding artery in the arterial phase, and the drainage vein becomes apparent in the venous phase, while the tumor demonstrates progressive hyperfluorescence with late leakage of dye into the surrounding structures [8]. In the two cases in this study, FFA examination showed that the typical feeding artery and drainage vein of the RH in the early-phase, and fluo-rescein leakage in the late-phase, was due to the vascular endothelial failure of the tumor.
The OCT findings in VHL have been published [9]. These include retinoschisis, epiretinal membranes, macular oedema and serous detachment. Optical coherence tomography demonstrated a foveal detachment in Case 1. The foveal detachment was due to fluid accumulation and macular oedema. Hyper reflectance was also observed under the cross-section of the RH upon OCT examination in Case 2. The authors consider that OCT is a useful diagnostic method in RH because it allows for the evaluation of peripheral tumors and macular complications, such as macular oedema, foveal detachment and epiretinal membranes.
Although RHs show a slow-growing pattern and are sometimes quiescent, they may lead to significant vision loss by causing cystoid macular oedema, and exudative and tractional retinal detachment [3]. It was believed that the primary reason for the vision loss in Case 1 was foveal detachment. The RH was close to the posterior pole in Case 1. In Case 2, the primary reason for the vision loss was optic nerve atrophy. The CNS hemangioblastoma operation may have led to optic nerve atrophy and vision loss in Case 2. Retinal hemangioblastomas were at the equator of the eye in Case 2. Germline mutations as a result of single nucleotide changes that were detected in these cases (c.202T>C, p.Ser68Pro) are reported in only two other cases in the literature [10] but, in these cases, no systemic involvement except RH was detected. The other details of these cases have not been mentioned in the literature. Although these two cases had the same mutation, renal involvement was detected in both cases and also CNS involvement in Case 2, in addition to RH.
Life-threatening diseases such as VHL can be diagnosed by ophthalmologists. The life expectancy of VHL patients is below the age of 50 because of RCC and CNS hemangioblastoma complications [11]. von Hippel-Lindau disease is a familial cancer syndrome; patients with VHL and at-risk family members of these patients should be followed by periodic screening programs and genetic analyses. Eventually, the development of early diagnosis methods in VHL, such as genetic analysis, may provide both superior visual prognosis and life expectancy. In conclusion, VHL patients who had a germline mutation resulting from a single nucleotide change in the
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.