Evidence map›Paper›PMID 42183084›Full record

ArticleFrontiers in ophthalmology2026

Poroid hidradenoma of the eyelid: a case report.

Christian Nieves-Rios, José J López-Fontanet, Juan Serrano-Olmo, Joseph Campbell

Abstract readCase Reports
In one paragraph

Article in Frontiers in ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Christian Nieves-RiosDepartment of Ophthalmology, School of Medicine, University of Puerto Rico, San Juan, Puerto Rico.
José J López-FontanetDepartment of Ophthalmology, School of Medicine, University of Puerto Rico, San Juan, Puerto Rico.
Juan Serrano-OlmoDepartment of Pathology, San Pablo Pathology Group, Bayamon, Puerto Rico.
Joseph CampbellDepartment of Ophthalmology, School of Medicine, University of Puerto Rico, San Juan, Puerto Rico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Poroid hidradenoma (PH) is a rare, benign tumor arising from eccrine sweat glands. It typically presents as a painless and slow-growing subcutaneous lesion in individuals in their sixth to seventh decades of life. Histologically, PH demonstrates neoplastic poroid cells with solid and cystic structures confined to the dermal layer, distinguishing it from other types of eccrine tumors such as eccrine poroma, hidroacanthoma simplex, and dermal duct tumor. It predominantly involves regions abundant in eccrine glands, yet reports involving the eyelids are scarce. Case presentation: We report a case of an 88-year-old woman with a 2-year history of a non-painful, enlarging mass on her left upper eyelid, associated with irritation and itchiness. Examination revealed a skin-colored, cystic lesion with associated madarosis and minimal telangiectasia. The patient underwent excisional biopsy of the lesion. Histopathological analysis confirmed the diagnosis of PH, characterized by well-circumscribed solid and cystic components with a pseudocapsule. There was no evidence of recurrence at the 3-month follow-up visit. Conclusion: This case highlights the rare occurrence of PH in the eyelids, emphasizing the diagnostic challenges associated with adnexal tumors in atypical locations. Surgical excision remains the standard treatment, and awareness of ocular manifestations of PH is essential for accurate diagnosis and management by ophthalmologists.

Indexed as

case reporteccrineeyelidhidradenomaporoid

Identifiers

PMID42183084
PMCPMC13189758

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