Kaplan M J, Sabio H, Wanebo H J, Cantrell R W
Laryngoscope. 1985 Jul;95(7 Pt 1):771-5.
The association of immunosuppression and head and neck cancer is supported by numerous reports demonstrating impaired cell-mediated immunity, depressed T-cell function, decreased lymphocyte responsiveness, and elevated circulating immune complexes. Fanconi's anemia (FA) is a rare autosomal recessive syndrome characterized by progressive pancytopenia, skeletal abnormalities, hyperpigmentation, and other congenital anomalies. Increased chromosomal instability and defective DNA repair have been uniform findings. Several reports suggest associated immune deficiencies. There is an increased frequency of leukemia, hepatocellular carcinoma, and squamous cell carcinoma (SCC), including six cases of head and neck SCC. We reported a young girl with FA who developed SCC of the tongue. Initial studies suggest low lymphocyte counts, but normal lymphocyte responsiveness. More precise characterization of the immune system defects in malignancy prone, genetically determined syndromes may provide clues for the diagnosis and treatment of patients with the more usual but more variable risk factors for SCC of the head and neck.
免疫抑制与头颈癌之间的关联得到了众多报告的支持,这些报告表明细胞介导的免疫功能受损、T细胞功能低下、淋巴细胞反应性降低以及循环免疫复合物升高。范可尼贫血(FA)是一种罕见的常染色体隐性综合征,其特征为进行性全血细胞减少、骨骼异常、色素沉着过度以及其他先天性异常。染色体不稳定性增加和DNA修复缺陷是一致的发现。有几份报告提示存在相关的免疫缺陷。白血病、肝细胞癌和鳞状细胞癌(SCC)的发病率增加,其中包括6例头颈SCC。我们报告了一名患有FA的年轻女孩,她患了舌部SCC。初步研究表明淋巴细胞计数低,但淋巴细胞反应性正常。对易患恶性肿瘤的遗传性综合征中的免疫系统缺陷进行更精确的表征,可能为诊断和治疗具有更常见但更具变异性的头颈SCC风险因素的患者提供线索。