Suzuki Daisuke, Kobayashi Ryoji, Yasuda Kazue, Nakagawa Atsuko, Morimoto Tsuyoshi, Yabe Miharu, Yabe Hiromasa, Kobayashi Kunihiko
Department of Pediatrics, Sapporo Hokuyu Hospital, Sapporo, Japan.
J Pediatr Hematol Oncol. 2011 Jan;33(1):22-4. doi: 10.1097/MPH.0b013e3181eb3153.
Lymphoid malignancies are rare in patients with Fanconi anemia (FA), particularly after bone marrow transplantation. A boy, who was diagnosed with FA at the age of 5; underwent successful bone marrow transplantation at the age of 11. One year later, he presented with fever and dry cough, and was found to have an anterior mediastinal tumor. Biopsy of the tumor revealed precursor-T cell lymphoblastic lymphoma. Human leukocyte antigen analysis confirmed that the tumor cells were derived from the patient's own cells. He received mild chemotherapy for lymphoma, but his condition deteriorated rapidly and he died from excessive chemotherapy-related toxicity. The literature contains no reports of successful chemotherapy for lymphoid tumors in patients with FA, and therefore, alternatives to chemotherapy should be considered in the treatment of such patients.
范可尼贫血(FA)患者发生淋巴系统恶性肿瘤较为罕见,尤其是在骨髓移植后。一名5岁时被诊断为FA的男孩,11岁时成功接受了骨髓移植。一年后,他出现发热和干咳,被发现患有前纵隔肿瘤。肿瘤活检显示为前体T细胞淋巴母细胞淋巴瘤。人类白细胞抗原分析证实肿瘤细胞来源于患者自身细胞。他接受了轻度的淋巴瘤化疗,但病情迅速恶化,最终死于化疗相关的毒性反应。文献中没有关于FA患者淋巴肿瘤化疗成功的报道,因此,在治疗此类患者时应考虑化疗以外的其他治疗方法。