Acute myeloid leukemia developed through myeloproliferative features during immunosuppressive therapy for juvenile idiopathic arthritis.

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL JOURNAL OF MEDICAL INVESTIGATION Pub Date : 2024-01-01 DOI:10.2152/jmi.71.335
Masahiro Oura, Ryohei Sumitani, Yusaku Maeda, Hikaru Yagi, Mamiko Takahashi, Takeshi Harada, Shiro Fujii, Hirokazu Miki, Taiki Hori, Jumpei Murai, Kumiko Kagawa, Masahiro Abe, Shingen Nakamura
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Abstract

A 17-year-old male with thrombocytosis and exacerbation of arthralgia during intensified immunosuppressive therapy with tocilizumab, prednisolone, and methotrexate for juvenile idiopathic arthritis (JIA) was referred to our department. Bone marrow examination revealed myelodysplastic syndrome/myeloproliferative neoplasm, unclassifiable (MDS/MPN-U). Peripheral myeloblasts disappeared temporarily after discontinuation of tocilizumab but progressed to acute myeloid leukemia six months after the development of MDS/MPN-U. The patient sustained complete remission after unrelated bone marrow stem cell transplantation, followed by chemotherapy. The arthralgia also improved after chemotherapy. The possibility of developing malignancies during immunosuppressive therapy in patients with JIA should be considered. J. Med. Invest. 71 : 335-339, August, 2024.

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在对幼年特发性关节炎进行免疫抑制治疗期间,因骨髓增生性特征而发展成急性髓性白血病。
一名17岁的男性因血小板增多和关节痛加重,在使用托西珠单抗、泼尼松龙和甲氨蝶呤加强免疫抑制治疗幼年特发性关节炎(JIA)期间转诊至我科。骨髓检查显示患者患有骨髓增生异常综合征/骨髓增生性肿瘤,无法分类(MDS/MPN-U)。停用托西珠单抗后,外周骨髓细胞暂时消失,但在出现MDS/MPN-U的六个月后发展为急性髓性白血病。患者在接受非亲缘骨髓干细胞移植和化疗后病情得到完全缓解。化疗后,关节痛也得到了改善。应考虑到JIA患者在接受免疫抑制治疗期间发生恶性肿瘤的可能性。J. Med.Invest.71 : 335-339, August, 2024.
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JOURNAL OF MEDICAL INVESTIGATION
JOURNAL OF MEDICAL INVESTIGATION MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.20
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0.00%
发文量
55
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