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鼻腔及鼻窦淋巴瘤:病例系列

Lymphoma of the nasal cavity and paranasal sinuses: A case series.

作者信息

Steele Toby O, Buniel Maria C, Mace Jess C, El Rassi Edward, Smith Timothy L

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of California Davis, Sacramento, California, USA.

出版信息

Am J Rhinol Allergy. 2016 Sep;30(5):335-9. doi: 10.2500/ajra.2016.30.4347.

Abstract

BACKGROUND

Lymphomas of the sinonasal tract are a rare and heterogeneous subset of solid sinonasal neoplasms.

OBJECTIVE

To characterize, in this case series, presenting symptoms, treatment modalities, and outcomes for patients with sinonasal lymphoma within a single institution.

METHODS

Retrospective patient data were collected from an academic, oncologic center and entered into a repository designed to capture outcomes for sinonasal malignancies. Patient demographics, presenting symptoms, imaging findings, treatment modalities, and health status were retrospectively extrapolated and evaluated by using Kaplan-Meier estimations for survival probability.

RESULTS

Patients with sinonasal lymphoma with a mean follow-up of 50 months were identified (n = 18). Histologic diagnosis included the following: diffuse large B-cell lymphoma (n = 9), natural killer/T-cell lymphoma (n = 5), follicular lymphoma (n = 1), T-cell lymphoma (n = 1), and lymphoma-not otherwise specified (n = 2). The most frequent presenting symptoms were nasal obstruction (78%), facial pain (72%), facial swelling (50%), and nasal discharge (44%). Treatment before lymphoma diagnosis included antibiotics (83%), oral steroids (22%), decongestants (22%), and topical steroids (11%). Treatment regimens after diagnosis included both chemotherapy (94%) and chemoradiotherapy (56%). Survival rates by lymphoma subtype were 56% for B-cell lymphoma and 40% for natural killer/T-cell lymphoma. Overall, 2- and 5-year survival rates were 67% and 50%, respectively. The combination of chemotherapy and radiation resulted in significantly higher survival rates (p ≤ 0.001) than chemotherapy alone.

CONCLUSION

Sinonasal lymphomas are characterized by meager survival rates, which differ by histopathologic subtype. The diagnosis of sinonasal lymphoma is challenging because symptoms frequently parallel those of chronic rhinosinusitis. Increased awareness of these rare malignancies may improve detection and more timely treatment. Clinical trial registration NCT01332136.

摘要

背景

鼻窦淋巴瘤是鼻窦实体肿瘤中一种罕见且异质性的亚型。

目的

在本病例系列中,描述单一机构内鼻窦淋巴瘤患者的症状、治疗方式及预后。

方法

从一家学术性肿瘤中心收集回顾性患者数据,并录入一个旨在记录鼻窦恶性肿瘤预后的数据库。通过使用Kaplan-Meier生存概率估计法,回顾性推断并评估患者的人口统计学特征、症状、影像学表现、治疗方式及健康状况。

结果

确定了平均随访50个月的鼻窦淋巴瘤患者(n = 18)。组织学诊断包括:弥漫性大B细胞淋巴瘤(n = 9)、自然杀伤/T细胞淋巴瘤(n = 5)、滤泡性淋巴瘤(n = 1)、T细胞淋巴瘤(n = 1)和未另行指定的淋巴瘤(n = 2)。最常见的症状为鼻塞(78%)、面部疼痛(72%)、面部肿胀(50%)和流涕(44%)。淋巴瘤诊断前的治疗包括抗生素(83%)、口服类固醇(22%)、减充血剂(22%)和局部类固醇(11%)。诊断后的治疗方案包括化疗(94%)和放化疗(56%)。B细胞淋巴瘤的生存率为56%,自然杀伤/T细胞淋巴瘤为40%。总体而言,2年和5年生存率分别为67%和50%。化疗与放疗联合使用的生存率显著高于单纯化疗(p≤0.001)。

结论

鼻窦淋巴瘤的特点是生存率低,且因组织病理学亚型而异。鼻窦淋巴瘤的诊断具有挑战性,因为其症状常与慢性鼻窦炎相似。提高对这些罕见恶性肿瘤的认识可能会改善检测并实现更及时的治疗。临床试验注册号NCT01332136。

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