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一例可能的慢性移植物抗宿主病多发性肌炎累及呼吸肌和躯干肌——综合诊断方法

A likely case of chronic graft-versus-host disease polymyositis affecting respiratory and truncal muscles - a comprehensive diagnostic approach.

作者信息

Tan Jing Yuan, Quek Jeffrey Kim Siang, Lee Ming, Chan Lai Peng, Hwang William Ying Khee, Lim Francesca Wei Inng, Ho Aloysius Yew Leng, Linn Yeh Ching, Goh Yeow Tee, Than Hein

机构信息

Department of Haematology, Singapore General Hospital, Singapore.

Department of Pathology, Singapore General Hospital, Singapore.

出版信息

Blood Cell Ther. 2024 Sep 6;7(4):106-110. doi: 10.31547/bct-2023-040. eCollection 2024 Nov 25.

Abstract

BACKGROUND

Muscle involvement, termed polymyositis, is an uncommon manifestation of graft-versus-host disease (GvHD) in which the upper and lower limbs are commonly affected. However, respiratory failure due to diaphragmatic weakness has rarely been reported. Diagnosis is usually based on a combination of elevated muscle enzyme levels in the blood, neurophysiological studies, and muscle biopsies.

CASE REPORT

A 23-year-old man who presented with Philadelphia chromosome (Ph)-positive chronic myeloid leukemia in myeloid blast crisis, underwent HLA-matched sibling (sister) hematopoietic stem cell transplantation. Six months post-transplant, he experienced bilateral arm pain and weakness, with an inability to raise his limbs against gravity. He was also unable to sit erect, and was dyspneic and hypoxic, thus requiring oxygen supplementation. Serum muscle enzyme levels were found to be markedly elevated. Magnetic resonance imaging showed a patchy hyperintense T2-weighted signal and enhancement in the muscle groups of the limbs, as well as in the psoas and erector spinae muscles. The electromyogram results were consistent with those of inflammatory myopathy. Muscle biopsy revealed extensive necrotizing myositis with extensive lymphocyte infiltration throughout the muscle fascicle. Additionally, fluorescence in situ hybridization (FISH) analysis demonstrated that 30% of the nuclei scored were in the muscle fibers of recipient XY origin, and 70% were in T-lymphocytes of donor XX origin. GvHD polymyositis was diagnosed, and the patient responded well to corticosteroids and extracorporeal photopheresis.

CONCLUSION

GvHD polymyositis can affect various muscle groups and results in various clinical presentations. In our case, truncal involvement resulting in an inability to sit erect was a unique presentation. Prompt diagnosis is important, and we have highlighted a comprehensive multimodal approach, including the potential use of FISH analysis, to aid in diagnosis.

摘要

背景

肌肉受累,即多发性肌炎,是移植物抗宿主病(GVHD)的一种罕见表现,通常累及上下肢。然而,因膈肌无力导致呼吸衰竭的情况鲜有报道。诊断通常基于血液中肌肉酶水平升高、神经生理学研究和肌肉活检相结合的结果。

病例报告

一名23岁男性,患有费城染色体(Ph)阳性慢性髓性白血病且处于髓系原始细胞危象期,接受了人类白细胞抗原(HLA)匹配的同胞(姐姐)造血干细胞移植。移植后6个月,他出现双侧手臂疼痛和无力,无法对抗重力抬起四肢。他还无法挺直坐姿,呼吸困难且缺氧,因此需要吸氧。发现血清肌肉酶水平显著升高。磁共振成像显示四肢肌肉群以及腰大肌和竖脊肌在T2加权像上呈斑片状高信号并强化。肌电图结果与炎性肌病相符。肌肉活检显示广泛的坏死性肌炎,整个肌束有广泛的淋巴细胞浸润。此外,荧光原位杂交(FISH)分析表明,所检测的细胞核中30%位于受体XY来源的肌纤维中,70%位于供体XX来源的T淋巴细胞中。诊断为GVHD多发性肌炎,患者对皮质类固醇和体外光化学疗法反应良好。

结论

GVHD多发性肌炎可累及不同肌肉群并导致多种临床表现。在我们的病例中,躯干受累导致无法挺直坐姿是一种独特的表现。及时诊断很重要,我们强调了一种综合的多模式方法,包括FISH分析的潜在应用,以辅助诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6550/11620988/b9c28dfc1802/2432-7026-7-4-0106-g001.jpg

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