Sclerochoroidal calcification (SCC) presents as flat or minimally elevated yellow placoid lesions, sometimes associated with gray lesions that are similar in appearance to senile scleral plaque. SCC is rare and frequently misdiagnosed. The majority of cases are idiopathic and present with normal calcium-phosphorus metabolism and without associated ophthalmic or systemic conditions.
The majority of patients diagnosed with SCC are caucasian and elderly. There is a slight female predisposition (approximately 60% of cases). Patients with previous systemic disorders that impact calcium-phosphorus metabolism are at higher risk of developing sclerochoroidal calcifications. These include hyperparathyroidism, pseudohypoparathyroidism, parathyroid adenoma, chondrocalcinosis, sarcoidosis, Gitelman syndrome, Bartter syndrome, pseudo-gout, chronic renal disease, hypophosphatemia, hypervitaminosis, and metabolic imbalance after diuretic use.
Development of SCC can occur in 3 ways:
- Dystrophic, and
Primarily, the pathogenesis of the disease is idiopathic. Idiopathic presentation is seen in patients within the primary risk groups. Dystrophic calcification is seen following large amounts of tissue damage and/or chronic inflammation. Metastatic presentation is seen in patients with conditions that create an atypical calcium-phosphorus metabolism.
Calcium deposition begins in the sclera and expands to the choroid. The white and yellow-colored calcium deposits manifest as yellow placoid lesions in diagnostic imaging. Lesions usually develop postequatorially and superotemporally; some have speculated that calcifications correspond to the insertion sites of the oblique extraocular muscles. According to the literature, around half of cases diagnosed are bilateral. Lesions have been classified into 4 categories depending upon contour on optical coherence tomography:
- Rocky-rolling, and
- Table mountain.
Due to the minimal symptoms associated with SCC, the condition is often found during unrelated clinical exams.
Patients are often asymptomatic and do not report ocular complaints. Patients do not typically show a change in visual acuity. However, there are several case reports of macular SCC associated with choroidal neovascularization or exudative retinal detachment resulting in decreased visual acuity. However, a large review of 179 eyes of 118 patients did not report hemorrhage, subretinal fluid, retinal pigment epithelial detachment, or choroidal neovascular membrane (CNVM) in any case. A long follow-up (mean 4 years) of these cases did not show enlargement of the lesion, hemorrhage, subretinal fluid, CNVM, vision loss, or decalcification. None of the cases needed treatment.
Ophthalmoscopy is sufficient for diagnosis. The fellow eye may also have a similar and symmetrical lesion. There may be multiple lesions which, however, are typically localized near the superotemporal arcade or at the equator. There might be atrophy of overlying choroid and/or retinal pigment epithelium. The lesions may be arranged in a ring-like configuration. Calcifications can also be detected by B-scan ultrasonography, optical coherence tomography, orbital computed tomography, fundus autofluorescence, fluorescein angiography, and indocyanine green angiography. Ophthalmoscopy can be unremarkable while ultrasound shows echogenic areas indicative of calcifications (hyperechoic lesion with acoustic shadow), due to deposition in the sclera not yet reaching the choroid.
Patients who are diagnosed with SCC should be screened for their calcium and phosphorus levels, complete blood count, and complete metabolic panel (paying attention to serum calcium and potassium) as well as magnesium, phosphorus, parathyroid hormone, blood pH, and urine calcium to distinguish from underlying systemic diagnoses.
The differential diagnosis for SCC includes choroidal metastases, lymphoma, melanoma, nevus, choroidal hemangioma, choroidal osteoma, choroidal granuloma (tuberculosis, sarcoid), dysmorphic calcification, and chorioretinitis. A distinguishing factor is that these lesions are choroidal while SCC lesions are primarily scleral. Choroidal osteoma is usually a solitary peripapillary lesion with sharp margins seen in young individuals, the ultrasonogram of which reveals calcification. There might be some areas of decalcification in longstanding choroidal osteomas. The risk of visual decline is higher presumably due to the posterior location and association with the choroidal neovascular membrane.
Parathyroid adenoma, Bartter, and Gitelman syndromes should be ruled out with testing due to complications associated with these diseases. Patients should be advised to return annually for a dilated eye exam to monitor the progression of the lesions, although there is no treatment other than correcting any metabolic imbalances.
Calcifications are commonly misdiagnosed, resulting in unnecessary testing and referral to retinal specialists. Lesions are typically located away from the macula and rarely encroach the fovea, therefore visual prognosis in patients is good and visual acuity usually remains unchanged.
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