Medina-Sanson Aurora, Chico-Ponce de León Fernado, Cabrera-Muñoz María de Lourdes, Gallegos-Castorena Sergio, Caltenco-Serrano Raul, Barragán-Pérez Eduardo
Department of Oncology, Hospital Infantil de México Federico Gomez, Dr. Marquez Num 162, Colonia Doctores, C.P. 06720, Distrito Federal, México.
Childs Nerv Syst. 2006 Oct;22(10):1364-8. doi: 10.1007/s00381-006-0093-8. Epub 2006 Apr 6.
Primary central nervous system lymphoma is a very rare condition in pediatric patients.
We describe the case of a 10-year old girl who presented with acute bilateral vision impairment. At the time of presentation, the only positive finding was optic disk swelling, and the brain MRI scan was normal. Seventeen months later, she developed a large-cell non-Hodgkin lymphoma in the brain, with no evidence of neoplasia elsewhere. Immunodeficiencies and Epstein-Barr virus infection could not be demonstrated. The patient was successfully treated with a combination of cyclophosphamide, etoposide, vincristine, methotrexate, and cytarabine, plus intrathecal chemotherapy. Craniospinal irradiation was not used.
The patient's condition is still in remission 68 months after completing the treatment.
This case is the only non-Hodgkin lymphoma with primary central nervous system location treated in our institution in the last 10 years and represents less than 0.5% of our non-Hodgkin lymphoma series. Due to its rare occurrence, not much is known about the clinical features and treatment outcome of primary central nervous system lymphoma in pediatric patients.
原发性中枢神经系统淋巴瘤在儿科患者中是一种非常罕见的病症。
我们描述了一名10岁女孩的病例,她出现急性双侧视力障碍。就诊时,唯一的阳性发现是视盘肿胀,脑部MRI扫描正常。17个月后,她脑部出现大细胞非霍奇金淋巴瘤,其他部位未发现肿瘤迹象。未发现免疫缺陷和爱泼斯坦 - 巴尔病毒感染。患者成功接受了环磷酰胺、依托泊苷、长春新碱、甲氨蝶呤和阿糖胞苷联合治疗,外加鞘内化疗。未使用全脑全脊髓放疗。
患者在完成治疗68个月后病情仍处于缓解期。
该病例是我们机构在过去10年中治疗的唯一一例原发性中枢神经系统定位的非霍奇金淋巴瘤,占我们非霍奇金淋巴瘤系列的比例不到0.5%。由于其罕见性,关于儿科患者原发性中枢神经系统淋巴瘤的临床特征和治疗结果知之甚少。