Su Zheng-Yan, Zhang Dong-Sheng, Zhu Mei-Qin, Shi Yan-Xia, Jiang Wen-Qi
State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, 510060, PR China.
Ai Zheng. 2007 Aug;26(8):919-22.
BACKGROUND & OBJECTIVE: Primary paranasal sinus lymphoma (PPSL) is a rare presentation of extranodal non-Hodgkin's lymphoma with a natural history distinct from other lymphomas. This study was to evaluate the clinical and pathologic characteristics, treatment outcomes and prognosis of PPSL.
The records of 14 PPSL patients, treated at Cancer Center of Sun Yat-sen University from 1994 to 2006, were analyzed.
The primary involvement sites included the maxillary sinus (11 cases), ethmoid sinus (2 cases), and sphenoid sinus (1 case). All patients were at stage I-II (Ann Arbor system). According to the AJCC TNM staging system, most patients had advanced T3-T4 disease. Of the 14 patients, 12 had B-cell PPSL, 1 had T-cell PPSL, and 1 had unclassified PPSL. The most common type was diffuse large B-cell PPSL (6 cases, 42.9%). Two patients underwent total maxillectomy and 12 underwent local excision or biopsy. All patients received chemotherapy and 6 received radiotherapy after chemotherapy. Both 5-year overall and event-free survival rates were 78.6%, with a median survival of 59.5 months(range, 2-192 months).
PPSL is an uncommon presentation of lymphoma characterized by bulky local disease. Diffuse large B-cell lymphoma is the most common histologic type and the maxillary sinus is the most common original site of PPSL. A combined-modality approach with systemic chemotherapy and local-regional radiation is recommended for PPSL patients. The prognosis of PPSL is relatively good.
原发性鼻窦淋巴瘤(PPSL)是结外非霍奇金淋巴瘤的一种罕见表现形式,其自然病史与其他淋巴瘤不同。本研究旨在评估PPSL的临床和病理特征、治疗结果及预后。
分析了1994年至2006年在中山大学肿瘤防治中心接受治疗的14例PPSL患者的病历资料。
主要受累部位包括上颌窦(11例)、筛窦(2例)和蝶窦(1例)。所有患者均处于Ⅰ - Ⅱ期(Ann Arbor分期系统)。根据美国癌症联合委员会(AJCC)TNM分期系统,大多数患者有进展期T3 - T4疾病。14例患者中,12例为B细胞型PPSL,1例为T细胞型PPSL,1例为未分类PPSL。最常见的类型是弥漫大B细胞型PPSL(6例,42.9%)。2例患者接受了全上颌骨切除术,12例接受了局部切除或活检。所有患者均接受了化疗,6例在化疗后接受了放疗。5年总生存率和无事件生存率均为78.6%,中位生存期为59.5个月(范围:2 - 192个月)。
PPSL是一种罕见的淋巴瘤表现形式,其特征为局部肿块较大。弥漫大B细胞淋巴瘤是最常见的组织学类型,上颌窦是PPSL最常见的原发部位。建议对PPSL患者采用全身化疗和局部区域放疗相结合的综合治疗方法。PPSL的预后相对较好。