Koshiishi Megumi, Sueki Yuki, Kawashima Ichiro, Nakajima Kei, Mitsumori Toru, Kirito Keita
Department of Hematology and Oncology, University of Yamanashi, Japan.
Intern Med. 2017 Sep 1;56(17):2335-2338. doi: 10.2169/internalmedicine.8706-16. Epub 2017 Aug 10.
The development of tumor lysis syndrome (TLS) in association with treatment for myeloproliferative neoplasms (MPNs) is relatively rare. We herein present the case of a post-polycythemia vera (PV) myelofibrosis patient with massive splenomegaly who developed laboratory TLS after treatment with ruxolitinib, a potent JAK1/JAK2 inhibitor. She also exhibited a rapid reduction of spleen volume. Our present case suggests the potential risk of TLS development after ruxolitinib treatment, particularly in patients with massive splenomegaly.
与骨髓增殖性肿瘤(MPN)治疗相关的肿瘤溶解综合征(TLS)的发生相对罕见。我们在此报告一例真性红细胞增多症(PV)后骨髓纤维化患者,该患者脾肿大明显,在接受强效JAK1/JAK2抑制剂鲁索替尼治疗后出现实验室检查提示的TLS。她的脾脏体积也迅速缩小。我们目前的病例提示鲁索替尼治疗后有发生TLS的潜在风险,尤其是在脾肿大明显的患者中。