2026, Number 1
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Rev Mex Cir Bucal Maxilofac 2026; 22 (1)
Extranodal nasal T/NK cell lymphoma. Clinical case presentation
Ibarra GF, Carrillo RJA, González BJ, García GJÁ, Fuentes SA, Espinosa BRV, Aguirre ME, Pastor FA, López CR, Guillén ZD
Language: Spanish
References: 16
Page: 21-25
PDF size: 1574.50 Kb.
ABSTRACT
Introduction: extranodal nasal T/NK cell lymphoma was described as a lethal midline granuloma in 1994 and classified within the group of non-Hodgkin lymphomas. In 2022, the WHO included it in the group of angiocentric immunoproliferative lesions of post-thymic T cells with Epstein-Barr virus positivity, changing its name to extranodal nasal T/NK cell lymphoma. Its prevalence compared to all lymphoma types is 1.5 to 2.6%.
Objective: to report a clinical case of extranodal nasal T/NK cell lymphoma, including its histological characteristics, treatment, and prognosis.
Case report: a 43-year-old male presented with a destructive midfacial lesion affecting the nasal septum, turbinates, paranasal sinuses, tympanic region, and mastoid process. He had no systemic diseases and a history of surgical procedures and antibiotic regimens without satisfactory response. A tissue biopsy was performed on the palate and mastoid
region with immunohistochemistry for cytotoxic markers
(CD56+, CD3+) and
in situ hybridization for EBER for small
RNAs encoded by the Epstein-Barr virus. The diagnosis
was confirmed based on its progressive and destructive
angioinvasion.
Conclusions: extranodal NK/T cell
lymphoma is a rare, aggressive neoplasm characterized
by an angiocentric granulomatous and angioinvasive
infiltrate, which causes necrosis and generally has an
aggressive course. Diagnosis is based on the duration
of the disease and clinical characteristics, as well as
paraclinical studies that should include serology, culture,
biopsy, and immunohistochemistry. Treatment includes
radiotherapy and adjuvant chemotherapy, depending on
the extent of the disease and the patient’s condition.
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