Extranodal NK/T-cell lymphoma, nasal type, presenting as a necrotic palatal ulcer.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2026-08-04 eCollection Date: 2026-01-01 DOI:10.22551/2026.51.1302.10343
Mahdiyeh Zarei, Arghavan Tonkaboni, Parastoo Sabouri
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Abstract

Extranodal natural killer/T-cell lymphoma (ENKTL), nasal type, is an aggressive Epstein-Barr virus (EBV)-associated lymphoma that predominantly involves the nasal cavity and upper aerodigestive tract. Primary oral manifestations are rare and may clinically mimic benign inflammatory or infectious conditions, resulting in delayed diagnosis. This report presents a rare case of ENKTL initially manifesting as a rapidly progressive necrotizing palatal ulcer. A 44-year-old man presented with a three-week history of a necrotic ulcer on the posterior hard palate. Imaging revealed extensive midfacial destruction, including palatal perforation, nasal septal erosion, turbinate destruction, ethmoidal involvement, and medial orbital wall extension. Histopathologic examination demonstrated atypical large lymphoid cells with extensive necrosis and infiltration into adipose and muscle tissue. Immunohistochemical staining demonstrated diffuse expression of LCA and CD3, focal expression of CD30, absence of CD20, ALK, and CD56 expression, and a high proliferative activity, as evidenced by a Ki-67 index of approximately 90%. Based on the histomorphologic and immunophenotypic features, extranodal NK/T-cell lymphoma was suspected. Chromogenic in situ hybridization (CISH) for Epstein-Barr virus-encoded RNA (EBER) demonstrated strong nuclear positivity in atypical lymphoid cells, confirming the diagnosis of ENKTL, nasal type. The patient achieved complete remission after chemotherapy; however, eight months later, the patient developed a systemic relapse that was diagnosed as peripheral T-cell lymphoma. This case highlights the diagnostic complexity of ENKTL presenting as a destructive palatal lesion. Comprehensive histopathologic evaluation, detailed immunophenotyping, and EBV confirmation by EBER are essential for accurate diagnosis and timely oncologic management. ENKTL should be considered in the differential diagnosis of rapidly progressive oral necrotic lesions unresponsive to conventional therapy.

结外NK/ t细胞淋巴瘤,鼻型,表现为坏死性腭溃疡。
结外自然杀伤/ t细胞淋巴瘤(ENKTL),鼻型,是一种侵袭性eb病毒相关淋巴瘤,主要累及鼻腔和上呼吸道消化道。原发性口腔表现罕见,临床上可能类似良性炎症或感染性疾病,导致诊断延迟。本文报告一例罕见的ENKTL,最初表现为快速进展的坏死性腭溃疡。一个44岁的男人提出了一个坏死性溃疡的后硬腭三周的历史。影像学显示广泛的面中破坏,包括腭穿孔、鼻中隔糜烂、鼻甲破坏、筛骨受累和眶内壁延伸。组织病理学检查显示非典型大淋巴样细胞广泛坏死并浸润到脂肪和肌肉组织。免疫组织化学染色显示LCA和CD3弥漫性表达,CD30局灶性表达,CD20、ALK和CD56表达缺失,Ki-67指数约为90%,具有高增殖活性。根据组织形态学和免疫表型特征,怀疑结外NK/ t细胞淋巴瘤。Epstein-Barr病毒编码RNA (EBER)的显色原位杂交(CISH)在非典型淋巴样细胞中显示强烈的核阳性,证实鼻部型ENKTL的诊断。化疗后患者完全缓解;然而,8个月后,患者出现全身复发,被诊断为外周t细胞淋巴瘤。本病例突出了ENKTL诊断的复杂性,表现为一种破坏性的腭病变。全面的组织病理学评估,详细的免疫分型,以及通过EBER确认EBV是准确诊断和及时肿瘤治疗的必要条件。在常规治疗无效的快速进展性口腔坏死病变的鉴别诊断中应考虑ENKTL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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