Management of Optic Disc Melanocytoma Associated with Choroidal Neovascularisation and Macular Detachment

Purpose: An optic disc melanocytoma is often considered a benign lesion, requiring only routine follow-up to assess possible progression to a malignant condition or development of a Choroidal Neovascular Membrane (CNVM) which can cause a drop in vision and eventually loss of sight if untreated. With the advent of imaging technology, the follow-up and monitoring of disease progression and therapeutic interventions have been made easier and more comprehensive. We investigated a patient with this lesion using Spectral Domain-optical Coherence Tomography (SD-OCT), autofluorescence imaging, fundus fluorescein angiography, and documented her response to treatment with intravitreal ranibizumab for secondary CNVM.

An optic disc melanocytoma is characteristically a benign lesion [1], with a potential for malignant transformation [2,3]. These dark brown to black colored tumors are usually located on the optic nerve head, and many a time, the asymptomatic nature [4] of this condition prompts discovery only on routine ophthalmic examination. Several complications such as retinal vein obstruction [5,6] optic nerve infiltration [7], tumor enlargement [3,8] or necrosis [4], and rarely even visual field defects [9,10] with eventual blindness [11], have been described by previous authors. This benign condition warrants close monitoring indefinitely due to the distinct, albeit small, possibility of the lesion turning malignant [3].

Ocular melanocytoma arises from the melanocytes of the Retinal Pigment Epithelium (RPE) and are usually located in the posterior pole. Often the full histopathological extent of the lesion might not be immediately obvious as it burrows beneath the retinal layers well past its exposed surface. This lesion has also been called a magnocellular nevus of the optic disc, stressing its benign nature.

Most melanocytomas are situated on the optic disc and if the patient is fortunate, will remain unobtrusive. Melanocytomas are rarely associated with secondary Choroidal Neovascular Membranes (CNVM) which may develop as a result of the neoplastic process breaching the integrity of the RPE. Once commenced, the neovascular process can threaten the fovea depending on its location. Subretinal haemorrhage and exudation will follow the occurrence of a CNVM, often causing a drastic worsening in vision. Different methods of managing CNVM in melanocytoma have been reported, ranging from photodynamic therapy to submacular surgery [12-14]. The discovery of anti-vascular Endothelial Growth Factor (VEGF) molecules has been a boon to the management of sight threatening intraocular neovascular processes. These agents target VEGF receptors, ultimately causing a decrease in angiogenesis. The current therapeutic benefit of anti-VEGF drugs like ranibizumab is that these agents can attack the inciting angiogenic factors without much collateral damage, yet as it is an invasive procedure, absolute certainty of the diagnosis and the benign nature of the lesion is necessary before the decision to treat with intravitreal injections is made.

We present the case of a 29 year old lady with an incidental melanocytoma of the optic disc and secondary CNVM, managed with intravitreal ranibizumab (Lucentis). The images that were obtained detailed the tracking of the melanotic pigments subretinally during and following treatment.

A 28 year old lady presented to us with complaints of sudden defective vision in the left eye (OS) of four days duration. She had no previous ophthalmic examination elsewhere prior to presentation. Her Best Corrected Visual Acuity (BCVA) was 6/6 in the right eye (OD) and 6/12 in OS. Anterior segment evaluation was within normal limits bilaterally. Fundus examination of OD was normal with a normal peripheral and posterior retina. OS showed a brownish black, horizontally oval lesion, measuring approximately 2mm x 2.5mm in size situated on the optic disc (Figure 1a). The anterior surface of the lesion was exposed to the vitreous cavity while the temporal margins were blurred suggesting that the lesion extended beyond its visible margin. This exposed surface was uneven and excavated. The lesion seemed to be choking the disc, with the nasal disc margin appearing edematous, and the retinal veins appearing tortuous and engorged as compared to the other eye. A rim of Subretinal Fluid (SRF) was present surrounding the optic disc (Figure 1b) and involving the macula. A focus of subretinal fibrin was present one disc diameter nasal to the fovea with surrounding subretinal haemorrhage, suggestive of a neovascular process. There were flecks of black pigment dusted over the retina inferior to the disc suggesting that pigment had detached from the main lesion and settled over the retina. Pigment migration could also be discerned subretinally, extending in a linear fashion downward from the optic disc. There was no orange pigmentation over the lesion which could suggest a malignancy. A visual field analysis using the HFA 30-2 protocol was performed and a nasal scotoma extending from the blind spot and involving fixation was seen. Spectral Domain-optical Coherence Tomography (SD-OCT) of the lesion (HRA+OCT Spectralis, Heidelberg Engineering) showed intense hyper reflectivity of the lesion which was extending subretinally temporal to the optic nerve head and measuring 3.2mm in horizontal and 2.9mm in vertical dimensions (Figures 1c-e). The posterior extent of the lesion could not be recorded as the pigment was highly reflective, casting a shadow over the deeper structures. Line scan of the macula revealed SRF which was clear for the most part but had hyper reflectivity corresponding to the area of fibrin suggestive of exudation (Figure 1e). There was SRF surrounding the optic nerve head and extending approximately 2 disc diameters inferior to it. Fundus Fluorescein Angiography (FFA) documented a hypofluorescent mass which remained hypofluorescent through all the angiographic phases (Figures 2a-f). But an adjacent area showed a fuzzy hyperfluorescence with leak in the late frames of the angiogram suggestive of a secondary type 2 CNVM. Autofluorescence imaging of the lesion revealed complete blockage of reflectance suggestive of an infiltrative lesion on the optic disc eroding anteriorly which corresponded to the exposed part of the melanocytoma seen clinically. Surrounding this was an area of hypoautofluorescence which corresponded to the part of the lesion which had burrowed intraretinally on OCT. Ultrasound B scan revealed a homogenously solid hyperechoiec lesion on the optic nerve head approximately 1.8mm x 2mm. The lesion was too small to demonstrate high internal reflectivity as is classically described. There was no associated choroidal excavation. Based on these observations, a diagnosis of optic disc melanocytoma and secondary CNVM was made.

 

Figure 1: a) Clinical features of left fundus at presentation. Note the pigmented melanocytoma on the optic disc with surrounding edema. Subretinal fibrin (black arrow) with adjacent subretinal hemorrhage is obvious; b) Infra-red image of the melanocytoma. The subretinal fluid surrounding the optic disc can be visualized (black arrow heads); c) Autofluorescence image of the optic nerve head lesion. The retinal component of the melanocytoma is intensely hypoautofluorescent (white arrow). The subretinal pigments tracking inferiorly from the lesion can also be seen (black arrow); d) SD-OCT image of the cross section at line d in 1c. The raised hyperreflective lesion on the optic nerve head with posterior back shadowing can be seen. Approximate horizontal diameter of the lesion is 2665μm. The retinal and choroidal components can be clearly seen; and e) SD- OCT image of the cross section at line e in 1c. Subretinal fluid with fibrin and hyper reflective point echoes (white arrow) lining the detachment suggestive of migrated pigment is well visualized.

 

The patient was treated with 1.25mg of intravitreal injection ranibizumab (Lucentis) 0.05ml in view of the active CNVM. One week after the injection, the subretinal haemorrhage and fibrin had diminished with the resolution of most of the SRF, leaving a small residual amount around the optic disc (Figures 3a-d). Her vision had improved to 6/6 in OS. Interestingly, we observed that there was a migration of pigments toward the fovea and inferiorly with the resolution of the fluid imaged with the SD-OCT and autofluorescence imaging (Figures 4a and b). At last follow up 6 months later, her BCVA was 6/6 in both eyes with fundus of OS showing a scarred CNVM with no subretinal fluid under the fovea, persistent disc edema and dispersed pigments from the exposed melanocytoma. The dimensions of the melanocytoma were constant with no change in size noted.

 

This case report illustrates the advantage of intraocular imaging in diagnosis and management of complicated ocular melanocytoma. Melanocytomas are likely to be unilateral, with preponderance in the female gender [3], as in our patient. One large series reported that visual symptoms were unusual [3], but our patient had visual complaints due to the development of a CNVM, prompting her visit to the ophthalmologist. It is well documented that even small optic disc melanocytomas can cause visual dysfunction by mechanical effects: optic disc compression causing vascular occlusions or nerve fiber layer defects [10,15]. There are also secondary effects causing visual disturbances such as tumor necrosis causing ischemic optic neuropathy [16] or CNVM development. Clinically, differentiating these tumors from melanomas can pose a challenge in spite of available guidelines to help make a clinical diagnosis [17]. Our patient had a characteristic solitary pigmented lesion on the optic disc which is virtually the pathognomonic presentation of melanocytomas. Yet there were other features which raised red flags such as dimensions more than 2mm, subretinal fluid (which can be indicative of malignant change [18]) surrounding the lesion and associated hemorrhage. A papillary or juxtapapillary choroidal melanoma is the closest differential diagnosis but it is often a challenge to differentiate these neoplasms from choroidal nevi, or juxtapapillary adenomas or hyperplasia of the retinal pigment epithelium. We could confirm a diagnosis of melanocytoma in our patient by SD-OCT and B-scan ultrasonography. The presence of a perifoveal secondary CNVM was confirmed by the FFA. This rare cause of visual dysfunction is a late warning sign of poor visual prognosis if it involves the macula. These secondary CNVMs are easily imaged by FFA and warrant prompt intervention. Previous authors have described the use of Photodynamic Therapy (PDT) [12], intravitreal pharmacotherapy with bevacizumab [14] and submacular surgery [13] for CNVM removal. In all of these patients the visual outcome encouraging, as the CNVM was managed before it caused permanent macular photoreceptor damage. Non-invasive therapy such as PDT, is best chosen for patients in whom there is the slightest doubt about malignant transformation, as this is the safest treatment for these eyes. But the cost of the treatment might be limiting factor. In other cases where there is no uncertainty in diagnosis, intravitreal anti-VEGF therapy is convenient as it is effective. The only concern is if the needle tract will be susceptible to involvement if the melanocytoma does undergo a malignant transformation. One of the common effects of mechanical compression can be a central retinal vein occlusion. Clinically, she also seemed to have a ‘choked disc’, which led us to consider the possibility of mechanical compression at the optic cup. This can also occur due to perilesional inflammation or tumor necrosis [19]. In our case, although there was optic disc edema and dilatation of the central retinal veins, the FFA did not show any evidence of decreased or delayed retinal vein filling or vascular perfusion although the veins appeared more tortuous when compared to the opposite side.

The results after the first injection were encouraging with a 2 line visual improvement and clinical resolution of the subretinal fluid confirmed by OCT. Of concern was the migration of the pigment in the subretinal space, toward the fovea, which was a risk that had to be taken. This tracking was well imaged by autofluorescence imaging. As there has been subjective improvement in vision and clinical improvement with regard to the CNVM, we can assume that intravitreal ranibizumab had achieved the therapeutic goal in this patient.

The clinical dilemma of whether a pigmented optic disc lesion is malignant or not can be resolved by correlating clinical features and advanced imaging techniques like SD-OCT. This will determine the decision of how to treat the secondary neovascular processes. In conclusion, we report that appropriate imaging and intravitreal anti-VEGF agents may be considered to manage secondary CNVM in cases of optic disc melanocytoma, with good therapeutic outcomes.