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Updated: Jun 21, 2026

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Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
Published on: August 9, 2024
Ophthalmic presentation of plasma cell neoplasm
Erica A Person1, David B Lyon, Mahendra K Rupani
1Department of Ophthalmology, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Ophthalmic Plastic and Reconstructive Surgery
|July 21, 2009
Summary
A rare plasma cell neoplasm in the lacrimal sac recurred locally and then appeared distantly in the humerus. The patient showed no signs of multiple myeloma during two years of follow-up.
Area of Science:
- Ophthalmology
- Oncology
- Pathology
Background:
- Plasma cell neoplasms are rare tumors.
- Lacrimal sac tumors are uncommon, with varied histopathology.
- Extramedullary plasma cell tumors can occur systemically.
Observation:
- A 64-year-old man presented with a plasma cell neoplasm in the right lacrimal sac.
- The initial tumor was treated with surgery and radiation, followed by a local recurrence that also responded to radiation.
- A distant plasma cell neoplasm developed in the humerus.
Findings:
- The patient experienced a localized lacrimal sac plasma cell neoplasm with both local and distant metastases.
- Despite the widespread nature of the plasma cell neoplasms, the patient showed no evidence of multiple myeloma.
- This case highlights the potential for plasma cell neoplasms to present in unusual locations and behave independently of systemic disease.
Implications:
- This case expands the understanding of the clinical spectrum of plasma cell neoplasms.
- It underscores the importance of thorough evaluation for systemic disease in patients with extramedullary plasma cell tumors.
- Further research into the pathogenesis and behavior of these rare neoplasms is warranted.
