Kielar R A
Arch Ophthalmol. 1978 Jul;96(7):1249-51. doi: 10.1001/archopht.1978.03910060075015.
A 3-year-old boy was admitted with an orbital apex syndrome that histologically was proven to be an undifferentiated lymphosarcoma. He subsequently developed systemic multifocal extranodal involvement and died eight months later. Clinical findings were consistent with those seen in Burkitt's lymphoma. Some, but not all, of the cytologic findings were characteristic of Burkitt's lymphoma.
一名3岁男孩因眶尖综合征入院，组织学检查证实为未分化淋巴瘤。随后，他出现全身多灶性结外受累，并在8个月后死亡。临床发现与伯基特淋巴瘤所见一致。部分（而非全部）细胞学发现具有伯基特淋巴瘤的特征。
