慢性移植物抗宿主病,表现为孤立性肌炎。

Ayako Yamamura, Takashi Hanada, Taichi Hirano, Kazuhito Tanaka, Nao Nishimura, Shinya Endo, Kenji Tokunaga, Yoshiki Mikami, Jun-Ichirou Yasunaga
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引用次数: 0

摘要

一名26岁的男性接受hla匹配的同胞异体外周血干细胞移植治疗KMT2A重排的急性髓系白血病,并保持完全缓解。移植后第338天,患者出现发热、肌痛和肌酐激酶明显升高。我们最初怀疑是药物引起的横纹肌溶解,并停药,但他的症状没有改善。肌肉活检中PD-1染色的免疫组织学结果可诊断为移植物抗宿主病(GVHD)相关的肌炎。在常规慢性GVHD治疗方案的基础上,强的松龙治疗肌炎。慢性GVHD单独伴有肌炎是罕见的,并且GVHD相关的肌炎由于缺乏特定的病理特征而难以与其他形式的肌炎区分。最近,PD-1和HLA-DR表达被报道为慢性gvhd相关性肌炎的特征。pd -1阳性细胞浸润的病理表现对本病例的诊断和治疗有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Chronic graft-versus-host disease manifesting as isolated myositis].

A 26-year-old man underwent HLA-matched sibling allogeneic peripheral blood stem cell transplantation for acute myeloid leukemia with KMT2A rearrangement and maintained complete remission. On day338 post-transplant, he developed fever, myalgia, and markedly elevated creatinine kinase. We initially suspected drug-induced rhabdomyolysis and stopped the offending drugs, but his symptoms did not improve. Immunohistological findings with PD-1 staining in a muscle biopsy led to the diagnosis of graft versus host disease (GVHD)-associated myositis. The myositis resolved with prednisolone treatment based on the conventional chronic GVHD treatment protocol. Chronic GVHD with myositis alone is rare, and GVHD-associated myositis has been difficult to differentiate from other forms of myositis due to its lack of specific pathological features. Recently, PD-1 and HLA-DR expression have been reported as characteristic features of chronic GVHD-associated myositis. The pathological finding of PD-1-positive cell infiltration was useful in diagnosis and treatment in our case.

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