Miyagi K, Mukawa J, Kinjo N, Horikawa K, Mekaru S, Nakasone S, Koga H, Higa Y, Naito M
Department of Neurosurgery, University of the Ryukyus School of Medicine, Okinawa, Japan.
Acta Neurochir (Wien). 1995;135(1-2):87-92. doi: 10.1007/BF02307420.
A 7-year and 11 month-old girl with cerebellar astrocytoma linked to familial ataxia-telangiectasia (AT) is presented. She was born as the 7th girl of a woman with aortic arch syndrome. Two elder sisters of the patient have ataxia telangiectasia. She had immunodeficiency, and cerebellar ataxia, but had no oculocutaneous telangiectasia. The risk of cancer developing in AT patients is about 1,200 times greater than that in age-matched controls. With regard to central nervous system tumours, seven primary tumours have been reported, such as 3 cases of medulloblastoma and 4 cases of glioma. Members of AT families who were under the age of 45 had a risk of dying of a malignant neoplasm five times greater than in the general population. However, there were no reports of glioma in AT families. In this case, it is suggested that IgA deficiency linked to familial AT may have contributed to the development of astrocytoma.
本文报告了一名7岁11个月大的女孩,患有与家族性共济失调毛细血管扩张症(AT)相关的小脑星形细胞瘤。她是一名患有主动脉弓综合征女性的第7个女儿。该患者的两个姐姐患有共济失调毛细血管扩张症。她有免疫缺陷和小脑共济失调,但没有眼皮肤毛细血管扩张症。AT患者患癌症的风险比年龄匹配的对照组高约1200倍。关于中枢神经系统肿瘤,已经报告了7例原发性肿瘤,如3例髓母细胞瘤和4例胶质瘤。45岁以下的AT家族成员死于恶性肿瘤的风险比一般人群高5倍。然而,AT家族中没有胶质瘤的报告。在这种情况下,提示与家族性AT相关的IgA缺乏可能促成了星形细胞瘤的发生。