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Extranodal natural killer/T-cell lymphoma presenting as orbital cellulitis
Hanis Zuhaimy1, Hayati Abdul Aziz1, Suresh Vasudevan1
1Ophthalmology Department, Hospital Sultanah Aminah Johor Bahru, Johor, Malaysia.
GMS Ophthalmology Cases
|February 15, 2017
Summary
Extranodal natural killer/T-cell lymphoma (NKTCL) can mimic orbital cellulitis and pansinusitis. This aggressive case highlights the importance of considering NKTCL in similar presentations.
Area of Science:
- Oncology
- Ophthalmology
- Otorhinolaryngology
Background:
- Extranodal natural killer/T-cell lymphoma (NKTCL) is a rare and aggressive hematologic malignancy.
- NKTCL often presents with non-specific symptoms, making early diagnosis challenging.
Observation:
- A 56-year-old male presented with acute orbital cellulitis and pansinusitis symptoms.
- Initial presentation included decreased visual acuity, proptosis, periorbital edema, and restricted extraocular movements.
- Despite conservative treatment, the patient showed no clinical improvement.
Findings:
- Biopsy of the ethmoidal sinus revealed extranodal NKTCL.
- Imaging confirmed orbital involvement, intracranial extension into the cavernous sinus, and meningeal involvement.
- The patient succumbed to the illness two months after diagnosis despite chemotherapy.
Implications:
- This case underscores NKTCL's potential to mimic common orbital and sinus conditions.
- Highlights the need for high clinical suspicion and prompt diagnostic workup for aggressive NKTCL.
- Emphasizes the poor prognosis associated with advanced-stage extranodal NKTCL.
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