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Epibulbar Subconjunctival Apocrine Hidrocystoma
Norman C Charles1,2, Leela V Raju1, Eleanore T Kim1
1Department of Ophthalmology.
Apocrine hidrocystomas are rare benign cystic tumors of sweat glands. This report details an exceptional case of an epibulbar subconjunctival apocrine hidrocystoma, offering insights into its presentation and pathology.
Area of Science:
- Ophthalmology
- Dermatology
- Oncology
Background:
- Apocrine hidrocystomas are benign cystic tumors originating from apocrine sweat glands.
- They typically manifest on the head and neck, with ophthalmic cases often near the eyelid margins.
Observation:
- A 57-year-old woman presented with a unique, mobile epibulbar subconjunctival apocrine hidrocystoma.
- The patient had no prior history of ocular trauma or surgery.
Findings:
- Histopathology revealed an empty cyst lined by double-layered cuboidal epithelium.
- The inner epithelial layer showed apical decapitation secretion, confirmed by PAS staining.
- Immunohistochemistry demonstrated positivity for cytokeratin-7, smooth muscle actin, D2-40, and CDGFP-15.
Implications:
- This case expands the known locations of apocrine hidrocystomas within the ocular adnexa.
- Understanding the histopathological and immunohistochemical features is crucial for accurate diagnosis of these rare orbital tumors.
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