Jaber Mohamed A, Hassan Mawada, Ingafou Mohamed, Elameen Alaa Mohamed
Department of Clinical Sciences, College of Dentistry, Ajman University, Ajman P.O. Box 346, United Arab Emirates.
Center of Medical and Bio Allied Health Sciences Research, Ajman University, Ajman P.O. Box 346, United Arab Emirates.
J Clin Med. 2024 Jan 3;13(1):267. doi: 10.3390/jcm13010267.
Intraoral adenoid cystic carcinoma (ACC) arising from minor salivary glands (MSG) is a rare malignancy associated with delayed diagnosis and unfavorable outcomes. This study aimed to comprehensively review ACC of MSGs, focusing on clinical characteristics, imaging modalities, treatment approaches, and long-term outcomes.
A systematic search was conducted in PubMed, Web of Science, and MEDLINE databases to identify relevant articles reporting cases of ACC of MSGs between January 1997 and March 2023. The study was registered in PROSPERO (ID: CRD42023449478). A total of 10 studies that met the inclusion criteria were selected for critical review. In total, 902 patients were diagnosed with ACC of MSGs with an age range of 44.3 to 63 years, and an average age of 56.6 years. The female to male ratio ranges from 1:1 to 2.4:1. Regarding the primary site of ACC, the palate was the most common location, accounting for 30.5% to 83.3%, followed by the buccal mucosa, floor of the mouth, and lip and the retromolar area. For histology, the solid mass pattern was the most prevalent, seen in 95.2% of patients, followed by the cribriform pattern. Regarding treatment modalities, surgery was the most common approach, applied in 76.3% of cases, with a combination of surgery and radiotherapy used in 29.0% of cases. A smaller fraction, 3.2%, received a combination of surgery, chemotherapy, and radiotherapy, and 8.3% underwent radiotherapy alone. Local recurrence rates varied between 1% and 28.5%, and distant metastasis occurred in 18.2% to 33.3% of cases, predominantly to lymph nodes (14.5%). An analysis of overall survival across various stages and patient numbers indicated a 5-year survival rate of 68.0%. The findings of this study provide valuable insights for physicians in making treatment decisions and emphasize the need for ongoing research and collaborative clinical efforts to improve the management and outcomes of this challenging disease.
ACC of MSGs is a multifaceted condition typically manifesting as asymptomatic enlargement and ulceration. This disease is marked by distinct histopathological patterns and perineural invasion (PNI). Recognizing these distinctive aspects is key in shaping the treatment plan, which can range from surgical procedures to radiation therapy, chemotherapy, and evolving targeted treatments. Continuous research and collaborative clinical efforts remain critical for ongoing progress in the treatment and management of this challenging condition.
起源于小唾液腺(MSG)的口腔腺样囊性癌(ACC)是一种罕见的恶性肿瘤,其诊断往往延迟,预后不佳。本研究旨在全面回顾小唾液腺腺样囊性癌,重点关注其临床特征、影像学检查方法、治疗方法及长期预后。
在PubMed、Web of Science和MEDLINE数据库中进行系统检索,以识别1997年1月至2023年3月期间报告小唾液腺腺样囊性癌病例的相关文章。该研究已在PROSPERO(ID:CRD42023449478)注册。共选择了10项符合纳入标准的研究进行严格审查。共有902例患者被诊断为小唾液腺腺样囊性癌,年龄范围为44.3至63岁,平均年龄为56.6岁。男女比例在1:1至2.4:1之间。关于腺样囊性癌的原发部位,腭部是最常见的部位,占30.5%至83.3%,其次是颊黏膜、口底、唇部和磨牙后区。在组织学方面,实性肿块型最为常见,见于95.2%的患者,其次是筛状型。在治疗方式上,手术是最常见的方法,76.3%的病例采用手术治疗,29.0%的病例采用手术联合放疗。一小部分患者(3.2%)接受了手术、化疗和放疗联合治疗,8.3%的患者仅接受了放疗。局部复发率在1%至28.5%之间,18.2%至33.3%的病例发生远处转移,主要转移至淋巴结(14.5%)。对不同分期和患者数量的总生存率分析表明,5年生存率为68.0%。本研究结果为医生做出治疗决策提供了有价值的见解,并强调需要持续开展研究和进行临床协作,以改善这种具有挑战性疾病的管理和治疗效果。
小唾液腺腺样囊性癌是一种多方面的疾病,通常表现为无症状性肿大和溃疡。这种疾病具有独特的组织病理学模式和神经周围浸润(PNI)。认识到这些独特方面是制定治疗计划的关键,治疗计划范围可从手术到放射治疗、化疗以及不断发展的靶向治疗。持续的研究和临床协作对于在这种具有挑战性疾病的治疗和管理方面取得持续进展仍然至关重要。