Pathological features of inflammatory myopathy as a manifestation of chronic graft-versus-host disease after allogeneic bone marrow transplantation

被引:2
|
作者
Shiota, Tomo [1 ]
Eura, Nobuyuki [1 ]
Hasegawa, Atsushi [2 ]
Kiriyama, Takao [1 ]
Sugie, Kazuma [1 ]
机构
[1] Nara Med Univ, Sch Med, Dept Neurol, 840 Shijo Cho, Kashihara, Nara 6348522, Japan
[2] Nara Med Univ, Sch Med, Dept Hematol, Kashihara, Nara, Japan
关键词
bone marrow transplantation (BMT); graft-versus-host disease (GVHD); inflammatory myopathy (IM); myelodysplastic syndrome (MDS); myxovirus resistance protein 1 (MxA); MEMBRANE ATTACK COMPLEX; MYOSITIS; POLYMYOSITIS; EXPRESSION;
D O I
10.1111/neup.12816
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic graft-versus-host disease (cGVHD) is the most important complication resulting in the death of bone marrow transplantation (BMT) survivors. It is also a relatively rare cause of inflammatory myopathy (IM). We report the case of a 46-year-old woman who developed severe cGVHD-related IM after BMT for myelodysplastic syndrome. She presented with severe muscle pain and weakness with cGVHD-related symptoms in other organs. Myopathological analysis showed moderate cell infiltration with remarkable necrotic and regenerative fibers. Sarcoplasm and capillaries expressed C5b9 and myxovirus resistance protein 1. Non-necrotic fibers in perifascicular regions expressed MHC-II. Steroid therapy did not sufficiently control cGVHD-related IM, and the patient was concurrently treated with an immunosuppressant. Our findings show that IM is a key manifestation of cGVHD and that the expression of interferon-inducible proteins in muscle pathology is useful for identifying cGVHD-related IM.
引用
收藏
页码:309 / 314
页数:6
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