Poroid hidradenoma of the eyelid: a case report - Scorecard - MDSpire

Poroid hidradenoma of the eyelid: a case report

  • By

  • Christian Nieves-Rios

  • José J. López-Fontanet

  • Juan Serrano-Olmo

  • Joseph Campbell

  • May 7, 2026

  • 0 min

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Clinical Scorecard: Poroid Hidradenoma in the Eyelid: A Case Study

At a Glance

CategoryDetail
ConditionPoroid Hidradenoma (PH)
Key MechanismsNon-cancerous neoplasm from eccrine sweat glands, characterized by solid and cystic formations.
Target PopulationIndividuals in their sixth to seventh decades of life, but can occur in a wide age range.
Care SettingOphthalmology and dermatology clinics.

Key Highlights

  • PH is a rare, benign neoplasm primarily affecting eccrine gland-rich areas.
  • Histopathological examination is crucial for accurate diagnosis.
  • Surgical excision is the standard treatment to prevent potential malignant transformation.
  • Recurrence is infrequent, with a follow-up showing no signs of recurrence in the presented case.

Guideline-Based Recommendations

Diagnosis

  • Histological examination is essential for diagnosis.
  • Immunohistochemical staining may assist in ambiguous cases.

Management

  • Surgical excision with clear margins (2–3 mm) is recommended.

Monitoring & Follow-up

  • Initial close monitoring for recurrent or atypically situated lesions, with biannual or annual assessments as needed.

Risks

  • Malignant transformation is rare, occurring in fewer than 1% of cases.

Patient & Prescribing Data

Older adults, particularly those in their sixth to seventh decades.

Surgical resection is effective, with low recurrence rates observed.

Clinical Best Practices

  • Recognize ocular signs of PH for accurate diagnosis.
  • Ensure thorough histopathological evaluation for definitive diagnosis.

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