Zagolski Olaf, Dwivedi Raghav C, Subramanian Somasundaram, Kazi Rehan
Department of Head & Neck, Medical Centre Medicina, Kraków, Poland.
J Cancer Res Ther. 2010 Jan-Mar;6(1):5-10. doi: 10.4103/0973-1482.63553.
Childhood head and neck cancers are relatively uncommon. Of all head and neck cancers occurring in children, non-Hodgkin's lymphoma (NHL) is the most common, others being rhabdomyosarcoma and nasopharyngeal carcinoma. In the head and neck region, sinuses are the second commonest primary site of NHL after neck lymph nodes. These can be of several different types depending on the predominant cell type and histologic appearance, the most common histological variant being diffuse large B-cell lymphoma. In an attempt to simplify the classification and to develop a universally acceptable classification and staging, they have been classified and staged numerous times over the last three decades, adding more confusion to the topic. Clinical presentations vary according to the histological type. The low grade lymphomas present with a nasal cavity or para-nasal sinus mass associated with obstructive symptoms and/or lymphadenopathy, while high grade lymphomas present with aggressive signs and symptoms including non-healing ulcer, epistaxis, septal perforation and bony destruction. The primary treatment consists of chemotherapy and / or radiation therapy, which is able to achieve remission in two-third of the patients, however, prognosis remains poor with cumulative five-year survival rates at about 30% for all the types of sino-nasal NHLs. Newer targeted therapy (monoclonal antibodies) and combination therapies (including stem cells) are currently being tested in order to improve survival rates in these patients. This article aims at providing an overview of clinico-epidemiologic characteristics, staging system currently in use, management, prognosis and possibilities of future research in the field of childhood sinonasal NHLs.
儿童头颈癌相对少见。在儿童发生的所有头颈癌中,非霍奇金淋巴瘤(NHL)最为常见,其他的有横纹肌肉瘤和鼻咽癌。在头颈部区域,鼻窦是继颈部淋巴结之后NHL的第二常见原发部位。根据主要细胞类型和组织学表现,这些可分为几种不同类型,最常见的组织学变异型是弥漫性大B细胞淋巴瘤。在过去三十年里,为了简化分类并制定一个普遍可接受的分类和分期方法,它们被多次分类和分期,这给该主题增加了更多混乱。临床表现因组织学类型而异。低级别淋巴瘤表现为鼻腔或鼻窦肿物,伴有阻塞性症状和/或淋巴结病,而高级别淋巴瘤表现为侵袭性体征和症状,包括不愈合溃疡、鼻出血、鼻中隔穿孔和骨质破坏。主要治疗包括化疗和/或放疗,三分之二的患者能够实现缓解,然而,所有类型的鼻窦NHL的累积五年生存率约为30%,预后仍然很差。目前正在测试更新的靶向治疗(单克隆抗体)和联合治疗(包括干细胞),以提高这些患者的生存率。本文旨在概述儿童鼻窦NHL领域的临床流行病学特征、目前使用的分期系统、治疗、预后以及未来研究的可能性。