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Peripapillary choroidal cavitation as a feature of pathological myopia

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© BMJ Publishing Group Limited 2023. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION A man in his 40s was referred for evaluation of peripapillary orange pigmentation… Click to show full abstract

© BMJ Publishing Group Limited 2023. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION A man in his 40s was referred for evaluation of peripapillary orange pigmentation in the left eye. His bestcorrected (−6.00 D) visual acuity was 6/6 in each eye. Anterior segments and intraocular pressures (IOP) were normal. He had a posterior vitreous detachment in his right eye with a treated retinal break and multiple bilateral myopiarelated features (axial length (AL) 25.5 mm). These included white without pressure, tilted optic nerve head (ONH) and peripapillary atrophy without myopic maculopathy. The most striking feature was unilateral (left) inferior peripapillary orange chorioretinal discolouration (figure 1). Spectral domain optical coherence tomography (OCT) demonstrated the absence of normal choroidal vasculature within this area, consistent with peripapillary choroidal cavitation (PCC, figure 2). Overlying outer retinal lamination was generally uninterrupted other than a focal vitreochoroidal ‘sinkhole’ connection. Visual field revealed a superior hemifield/arcuate scotoma consistent with a tilted ONH. PCC (formerly peripapillary detachment in pathological myopia or intrachoroidal cavitation) is an anatomical choroidal modification (53% unilateral) typically associated with axial myopia (−9 to −12.5 D, AL ~27 mm), although emmetropia/ hyperopia accounts for ~7%. High myopia (≤−6 D) is associated with younger PCC presentation. The classic en face appearance is a nonelevated yelloworange peripapillary area most often inferior to a tilted ONH. 3 PCC may affect up to 50% of high myopia and 10% of low myopia. 5 6 OCT has been instrumental in delineating the anatomical layer responsible for the en face appearance. A hyporeflective appearance is seen at the level of the choroid, with posterior scleral deformation and/or a fullthickness neurosensory retina/retinal pigment epithelium defect contiguous between the choroidal and vitreous cavities (16%–25%). 3 Multiple choroidal schises can be noticed alongside cavitations potentially representing a precursor lesion. Early hypofluorescence on fluorescein angiography confirms absence of choroidal tissue/ circulation unless choroidal neovascularisation is present where OCT angiography may help delineate the neovascular complex. 7 Other pathological myopia features may be present, including tilted ONH (69%), peripapillary atrophy (98%), posterior staphylomata (40%), myopic maculopathy (14%–37%), peripheral retinal degenerations/ breaks, PVD and glaucoma (38%–70%). 5 Clinically, these cases may be referred for concern of amelanotic choroidal nevus/melanoma; however, multimodal imaging helps to clarify their ‘cystic’ rather than solid nature. Although thought to be acquired rather than congenital lesions, PCC development is gradual (no change over 6year followup). The pathogenesis may be related to myopia (ie, increased AL influences angle of optic nerve entry) and ageing (few PCC cases described <30 years of age). Loss of choroidal adhesion (ie, tissues Figure 1 Colour fundus photographs (TRC50DX, Topcon, Tokyo, Japan) of the right (A) and left (B) optic nerve heads (ONH) demonstrating myopic changes on the left including tilted ONH, peripapillary atrophy and orange discolouration at the inferior disc margin. Widefield fundus autofluorescence (‘California’, Optos, Dunfermline, UK) of the right (C) and left (D) eyes showing no gross abnormalities of the retinal pigment epithelium.

Keywords: choroidal cavitation; peripapillary choroidal; myopia; pathological myopia

Journal Title: BMJ Case Reports
Year Published: 2023

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