Janic Dragana, Dokmanovic Lidija, Jovanovic Nada, Lazic Jelena
Department of Hematology/Oncology, University Children's Hospital, Belgrade, Serbia.
J Pediatr Hematol Oncol. 2007 Oct;29(10):713-5. doi: 10.1097/MPH.0b013e31814d67f4.
We present a patient with acute lymphoblastic leukemia and ataxia-telangiectasia (A-T). The 4-year-old girl is the first child of young nonconsanguineous parents of Serbian origin. Gait problems appearing in the second year of life were treated by physiotherapy. At the age of 4 she was diagnosed with T-cell acute lymphoblastic leukemia and treated according to Berlin-Frankfurt-Munster strategy. Owing to typhlitis developing after 15 days of cytotoxic treatment, frequent radiologic examinations were performed causing profound aplasia. Typhlitis did not respond to conservative treatment but necessitated extensive bowel resection. At that time the A-T was suspected by our team and confirmed by increased chromosomal radiosensitivity and markedly reduced level of A-T mutated protein. Chemotherapy was continued without alkylating agents and further radiologic imaging ran an uncomplicated course. At present, the patient is in first remission and 2.5 years since the beginning of the treatment. We stress the importance of careful initial neurologic evaluation of children with malignancy.
我们报告一例患有急性淋巴细胞白血病和共济失调-毛细血管扩张症(A-T)的患者。这名4岁女孩是一对年轻的非近亲塞尔维亚裔父母的第一个孩子。在她1岁时出现的步态问题接受了物理治疗。4岁时,她被诊断为T细胞急性淋巴细胞白血病,并按照柏林-法兰克福-明斯特方案进行治疗。在细胞毒性治疗15天后发生了盲肠炎,频繁的放射学检查导致严重的再生障碍。盲肠炎对保守治疗无反应,需要进行广泛的肠切除术。当时我们团队怀疑患有A-T,并通过染色体放射敏感性增加和A-T突变蛋白水平显著降低得到证实。化疗在不使用烷化剂的情况下继续进行,进一步的放射学检查过程顺利。目前,患者处于首次缓解期,自治疗开始已过去2.5年。我们强调对患有恶性肿瘤的儿童进行仔细的初始神经学评估的重要性。