Spitz nevus arising in the eyelid of a teenager.

A 16-year-old boy developed over a 2-month interval a lightly pigmented left upper eyelid lesion measuring 1.5 mm in greatest diameter that, when excised, microscopically was hypercellular and composed almost exclusively of nonpigmented epithelioid cells that created florid, large intraepidermal junctional nests and sheets and nests of subepidermal cells. The diagnosis was a Spitz nevus.

CLASSIFICATION OF SCLEROCHOROIDAL CALCIFICATION BASED ON ENHANCED DEPTH IMAGING OPTICAL COHERENCE TOMOGRAPHY "MOUNTAIN-LIKE" FEATURES.

Purpose: To describe distinct enhanced depth optical coherence tomography patterns of sclerochoroidal calcification and their correlation to clinical features.

Methods: Retrospective chart review of 67 eyes of 46 patients with spectral domain optical coherence tomography imaging.

Results: The mean patient age at diagnosis was 68 years.

Sclerochoroidal calcification: clinical features, outcomes, and relationship with hypercalcemia and parathyroid adenoma in 179 eyes.

Purpose: To describe the clinical features and long-term ophthalmic and systemic findings in patients with sclerochoroidal calcification (SCC).

Methods: Retrospective non-interventional clinical chart review of 179 eyes of 118 patients with SCC to evaluate for the relationship of SCC with systemic calcium metabolic abnormalities.

Results: The mean patient age at diagnosis was 69 years.

Review of cystic and solid tumors of the iris.

Iris tumors are broadly classified into cystic or solid lesions. The cystic lesions arise from iris pigment epithelium (IPE) or iris stroma. IPE cysts classically remain stable without need for intervention.

Clinical survey of 3680 iris tumors based on patient age at presentation.

Objective: To report the spectrum of iris lesions based on patient age at presentation.

Design: Retrospective, nonrandomized, single-center case series.

Participants: We included 3680 iris tumors in 3451 patients.