Behrendt H, de Korte D, van Gennip A H, van Leeuwen E F
Emma Kinderziekenhuis and Antoni van Leeuwenhoekziekenhuis, The Netherlands Cancer Institute, Amsterdam.
Pediatr Hematol Oncol. 1987;4(3):261-7. doi: 10.3109/08880018709141276.
A case of eosinophilic meningitis 2 months before the appearance of lymphoblasts in the cerebrospinal fluid is described in a child with acute lymphoblastic leukemia (ALL). The peripheral blood showed no simultaneous eosinophilia. The child was successfully treated for her CNS relapse, and complete remission was easily obtained. The eosinophils and lymphoblasts disappeared quickly after the administration of intrathecal methotrexate. However, 3 1/2 years later hypereosinophilia developed in the blood and bone marrow, heralding bone marrow relapse. Simultaneously, meningeal relapse was diagnosed and this time the cerebrospinal fluid showed a mixture of lymphoblasts and eosinophils. Treatment was reinstituted and complete remission was again obtained. Analysis of the blood eosinophils showed abnormal nucleotide patterns. Similar patterns were previously found in the lymphoblasts from other ALL patients.
一名急性淋巴细胞白血病(ALL)患儿在脑脊液中出现成淋巴细胞前2个月发生了嗜酸性粒细胞性脑膜炎。外周血未同时出现嗜酸性粒细胞增多。该患儿的中枢神经系统复发得到了成功治疗,且很容易就获得了完全缓解。鞘内注射甲氨蝶呤后,嗜酸性粒细胞和成淋巴细胞迅速消失。然而,3年半后,血液和骨髓中出现了嗜酸性粒细胞增多,预示着骨髓复发。同时,诊断出脑膜复发,此次脑脊液中显示有成淋巴细胞和嗜酸性粒细胞混合存在。再次进行治疗并再次获得完全缓解。对血液嗜酸性粒细胞的分析显示出异常的核苷酸模式。此前在其他ALL患者的成淋巴细胞中也发现过类似模式。