Beckhardt R N, Weber R S, Zane R, Garden A S, Wolf P, Carrillo R, Luna M A
Department of Head and Neck Surgery, University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.
Laryngoscope. 1995 Nov;105(11):1155-60. doi: 10.1288/00005537-199511000-00003.
Minor salivary gland tumors of the palate are rare and may pose a diagnostic and therapeutic dilemma for the head and neck surgeon. The authors reviewed their 46 years of experience with minor salivary gland tumors of the palate to determine the factors that influence outcome and their implications for treatment. Malignant tumors were seen in 116 patients (78%) and benign tumors were found in 33 patients (22%). Adenoid cystic carcinoma was the most common malignant tumor, occurring in 43 patients, and pleomorphic adenoma was the most common benign tumor, occurring in 30 patients. Univariate analysis on the malignant lesions showed that grade 3 tumor histology (P < .001), tumor size greater than 3 cm (P < .001), perineural invasion (P = .031), bone invasion (P = .012), positive surgical margins (P < .001), and positive initial but negative final margins (P = .004) were all associated with decreased survival. With multivariate analysis, tumor size, margin status, and grade were shown to be independently associated with decreased survival (P < .05). The recurrence rate at the primary site was significantly higher for adenoid cystic carcinoma than for other histologies (P = .0059). The 2-, 5-, and 10-year disease-specific survival rates for patients with malignant disease were 96%, 87%, and 80%, respectively. Wide surgical excision with adequate margins is essential for a favorable outcome in patients with malignant minor salivary gland tumors. Postoperative radiotherapy is reserved for patients with grade 3 tumor histology, large primary lesions, perineural invasion, bone invasion, cervical lymph node metastasis, and positive margins, although a clear-cut survival advantage has not been proven. Recurrence, especially regional and distant metastasis, portends an extremely poor prognosis.
腭部小唾液腺肿瘤较为罕见,可能会给头颈外科医生带来诊断和治疗上的难题。作者回顾了他们46年来治疗腭部小唾液腺肿瘤的经验,以确定影响预后的因素及其对治疗的意义。116例患者(78%)为恶性肿瘤,33例患者(22%)为良性肿瘤。腺样囊性癌是最常见的恶性肿瘤,有43例;多形性腺瘤是最常见的良性肿瘤,有30例。对恶性病变的单因素分析显示,3级肿瘤组织学(P < .001)、肿瘤大小大于3 cm(P < .001)、神经侵犯(P = .031)、骨侵犯(P = .012)、手术切缘阳性(P < .001)以及初始切缘阳性但最终切缘阴性(P = .004)均与生存率降低相关。多因素分析显示,肿瘤大小、切缘状态和分级与生存率降低独立相关(P < .05)。腺样囊性癌的原发部位复发率显著高于其他组织学类型(P = .0059)。恶性疾病患者的2年、5年和10年疾病特异性生存率分别为96%、87%和80%。对于恶性腭部小唾液腺肿瘤患者,进行足够切缘的广泛手术切除对于获得良好预后至关重要。术后放疗适用于3级肿瘤组织学、原发灶较大、神经侵犯、骨侵犯、颈部淋巴结转移和切缘阳性的患者,尽管尚未证实其有明确的生存优势。复发,尤其是区域和远处转移,预示着预后极差。