A Large Infantile Capillary Hemangioma of the Eyelid with 5 Years Follow-up

Mohammad Idris1, Mahfooz Hussain1, Junaid Sethi1

  • 1Department of Ophthalmology, Lady Reading Hospital/MTI, Peshawar, Pakistan.

Insights

A congenital eyelid mass in a newborn girl did not respond to intralesional triamcinolone acetonide or oral propranolol. Surgical excision was performed, but the tumor recurred, highlighting challenges in managing orbital tumors.

Area of Science:

  • Ophthalmology
  • Pediatric Oncology
  • Dermatology

Background:

  • Congenital eyelid masses can cause significant visual obstruction in infants.
  • Early intervention is crucial for preserving vision and cosmesis.
  • Treatment options for orbital tumors in neonates are varied and require careful consideration.

Observation:

  • A five-day-old infant presented with a large right upper and lower eyelid mass.
  • The mass completely obstructed the visual axis, posing a risk to vision.
  • Initial treatment included intralesional triamcinolone acetonide under general anesthesia, with no observed tumor size change.

Findings:

  • Systemic propranolol (1 mg/kg) was administered at three months of age.
  • No significant reduction in tumor size was noted after two months of propranolol therapy.
  • Surgical excision was performed, but the tumor demonstrated recurrence post-operatively.
  • Neither intralesional triamcinolone acetonide nor oral propranolol showed efficacy in managing this eyelid tumor.

Implications:

  • This case underscores the limited efficacy of non-surgical treatments like intralesional triamcinolone acetonide and oral propranolol for certain congenital eyelid tumors.
  • Recurrence after surgical excision suggests the need for further investigation into the tumor's biology and potentially more aggressive or targeted therapeutic strategies.
  • Further research is warranted to identify optimal management protocols for recurrent or refractory congenital eyelid masses to prevent long-term visual impairment.

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