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Natural killer/T-cell lymphoma invading the orbit and globe
Lance J Lyons1, Ivan Vrcek1, Marie Somogyi1
1University of Texas at Austin Dell Medical School, Austin, Texas (Lyons); TOC Eye and Face, Austin, Texas (Vrcek, Somogyi, Nakra); ENT and Allergy Center of Austin, Round Rock, TX (Taheri); Seton Medical Center Austin, Austin, Texas (Admirand); Retina Consultants of Austin, Austin, Texas (Chexal); and Texas Oncology, Austin, Texas (Loukas).
Natural killer/T-cell lymphoma is a rare cancer, often seen in Asian and South American patients and linked to Epstein-Barr virus. This case report details a Vietnamese woman with orbital and conjunctival involvement, emphasizing diagnostic challenges.
Area of Science:
- Oncology
- Pathology
Background:
- Natural killer/T-cell lymphoma (NKTL) is a rare extranodal lymphoma with a poor prognosis.
- Epidemiological studies indicate a predilection for Asian and South American populations and a strong association with Epstein-Barr virus (EBV).
Observation:
- A 78-year-old Vietnamese woman presented with unexplained vitritis.
- Disease progression led to the development of proptosis and conjunctival lesions.
- Biopsies from the orbit, ethmoid sinus, and conjunctiva confirmed NKTL.
Findings:
- The patient's presentation mimicked other orbital and ocular inflammatory or neoplastic conditions.
- Histopathological examination was crucial for definitive diagnosis of NKTL.
Implications:
- This case underscores the diagnostic challenges posed by rare malignancies like NKTL.
- Early recognition and accurate diagnosis are critical for appropriate management and improved outcomes in NKTL patients.
- Highlights the importance of considering NKTL in the differential diagnosis of unexplained orbital and ocular symptoms, particularly in endemic populations.
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