ebv阳性鼻咽癌模拟唾液腺肿瘤的网状和黏液样变异:一个病例系列。

Che-Chi Liao, Ying-Ju Kuo, Yen-Wen Lu, Ko-Hung Shen, Shiuan-Li Wey, Ren-Ching Wang, Nien-Yi Chang, Min-Shu Hsieh, Yun-An Chen
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引用次数: 0

摘要

目的:本研究旨在描述一种罕见的鼻咽癌形态变异,即网状和黏液样鼻咽癌(RMNK-NPC),由于其与唾液腺肿瘤的相似性,给诊断带来了挑战。我们试图详细介绍其组织病理学和免疫组织化学特征,澄清鉴别诊断,并评估临床结果。方法:回顾性分析台湾地区RMNK-NPC的病理会诊档案和多学科会议记录。三位病理学家回顾了组织病理学特征,包括先前进行的免疫组织化学染色和eb病毒编码RNA (EBER)原位杂交的结果。收集相关的临床资料和影像学结果。进行文献检索以确定先前报道的具有相似组织学特征的病例。结果:纳入8例患者(男性7例,女性1例;中位年龄65.5岁)。临床表现包括7例晚期肿瘤伴淋巴结转移和2例远处转移。所有肿瘤均表现为黏液样间质,上皮样细胞呈网状、小梁状和索状排列到梭形细胞,其中3例转变为非角化鳞癌(NKSCC)。免疫组化显示泛细胞角蛋白和鳞状标记物一致呈阳性,而除SOX10外,其他肌上皮标记物大多呈阴性。大多数病例显示强烈的核阳性,证实了EBV的相关性。4名接受放化疗的患者的有限随访数据显示,2名患者在3-4个月时病情稳定。另外两名患者分别在42个月和108个月时死于无关原因,未观察到复发。结论:RMNK-NPC代表ebv相关的NPC,具有独特的组织形态,与唾液腺肿瘤重叠。准确的诊断依赖于全面的免疫组化和EBER ISH。认识这一实体对于避免误诊和指导适当治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reticular and Myxoid Variant of EBV-positive Nasopharyngeal Carcinoma Mimicking Salivary Gland Tumors: A Case Series.

Purpose: This study aims to characterize the rare morphological variant of nasopharyngeal carcinoma known as reticular and myxoid nasopharyngeal carcinoma (RMNK-NPC), which poses diagnostic challenges due to its resemblance to salivary gland tumors. We seek to detail its histopathological and immunohistochemical features, clarify differential diagnoses, and evaluate clinical outcomes.

Methods: Cases of RMNK-NPC were retrospectively identified from pathology consultation archives and multidisciplinary conference records in Taiwan. Histopathological features, including results of previously performed immunohistochemical stains and Epstein-Barr virus-encoded RNA (EBER) in situ hybridization, were reviewed by three pathologists. Relevant clinical information and imaging findings were collected when available. A literature search was conducted to identify previously reported cases with similar histological features.

Results: The cohort included eight patients (7 males, 1 female; median age 65.5 years). Clinical presentations included advanced-stage tumors with lymph node metastases in seven patients and distant metastasis in two patients. All tumors exhibited myxoid stroma with reticular, trabecular, and cord-like arrangements of epithelioid to spindle cells, with transition to non-keratinizing squamous cell carcinoma (NKSCC) in three cases. Immunohistochemistry showed consistent positivity for pan-cytokeratin and squamous markers, while other myoepithelial markers were mostly negative, except SOX10. EBER ISH showed strong nuclear positivity in most cases, confirming EBV association. Limited follow-up data for four patients who received chemoradiotherapy showed stable disease at 3-4 months in two. The other two patients died at 42 and 108 months, respectively, from unrelated causes, with no recurrence observed.

Conclusion: RMNK-NPC represents an EBV-associated NPC with unique histomorphology that overlaps with salivary gland tumors. Accurate diagnosis relies on comprehensive immunohistochemical panels and EBER ISH. Awareness of this entity is crucial to avoid misdiagnosis and guide appropriate treatment.

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