A Case of Orbital Lipoblastoma: Temporal Evolution of Imaging Findings

Insights

Orbital lipoblastoma, a rare tumor, was diagnosed in an infant presenting with an eyelid mass. This case highlights the tumor's clinical, radiological, and histopathological features in the orbit.

Area of Science:

  • Ophthalmology
  • Pediatric Oncology
  • Pathology

Background:

  • Lipoblastoma is a rare benign tumor of adipocytes, typically occurring in infants and children.
  • Orbital involvement is exceptionally uncommon, making this case noteworthy.

Observation:

  • A 3-month-old male infant presented with a palpable left upper eyelid mass.
  • Serial magnetic resonance imaging (MRI) was performed over a 1-year observation period.
  • An excisional biopsy was conducted at 15 months of age.

Findings:

  • Histopathology revealed hypocellular lobules with varied adipocyte maturity and myxoid stroma.
  • Prominent fibrous septa were noted, consistent with lipoblastoma.
  • Radiological-pathological correlation was established for this orbital lipoblastoma.

Implications:

  • This case expands the understanding of lipoblastoma presentation in the orbital region.
  • It underscores the importance of comprehensive evaluation for rare pediatric orbital masses.
  • Highlights the utility of serial imaging and histopathology in diagnosis.

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