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抗线粒体抗体阳性的炎性肌病中的空泡性病理改变。

Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy.

机构信息

Department of Neurology, Peking University First Hospital, No.8 Xishiku Street, Xicheng District, Beijing, 100034, China.

Department of Radiology, Peking University First Hospital, No.8 Xishiku Street, Xicheng District, Beijing, 100034, China.

出版信息

BMC Musculoskelet Disord. 2024 Apr 2;25(1):257. doi: 10.1186/s12891-023-06941-6.

Abstract

BACKGROUND

A few patients with inflammatory myopathy showed anti-mitochondrial antibody (AMA) positivity. This study aimed to report the clinical and pathological findings with vacuoles in 3 cases of such patients.

METHODS

Three cases with myositis from the Myositis Clinical Database of Peking University First Hospital were identified with AMA positivity. Their clinical records were retrospectively reviewed and the data was extracted. All the 3 cases underwent muscle biopsy.

RESULTS

Three middle-aged patients presented with chronic-onset weakness of proximal limbs, marked elevation of creatine kinase, and AMA-positivity. Two of the 3 cases meet the criteria of primary biliary cholangitis. All the 3 cases presented with cardiac involvement and proteinuria. Two cases developed type 2 respiratory failure. MRI of the thigh muscle showed multiple patches of edema bilaterally in both cases, mostly in the adductor magnus. Pathological findings include degeneration of muscle fibers, diffused MHC-I positivity, and complement deposits on cell membranes. Vacuoles without rims of different sizes were discovered under the membrane of the muscle fibers. A few RBFs were discovered in case 1, while a diffused proliferation of endomysium and perimysium was shown in case 2.

CONCLUSIONS

AMA-positive inflammatory myopathy is a disease that could affect multiple systems. Apart from inflammatory changes, the pathological findings of muscle can also present vacuoles.

摘要

背景

少数炎性肌病患者表现出抗线粒体抗体(AMA)阳性。本研究旨在报告 3 例此类患者伴有空泡的临床和病理发现。

方法

从北京大学第一医院肌炎临床数据库中确定了 3 例 AMA 阳性的肌炎病例。回顾性复习了他们的临床记录并提取了数据。所有 3 例患者均接受了肌肉活检。

结果

3 例中年患者表现为四肢近端进行性无力、肌酸激酶显著升高和 AMA 阳性。其中 2 例符合原发性胆汁性胆管炎的标准。所有 3 例均有心脏受累和蛋白尿。2 例发生 2 型呼吸衰竭。大腿肌肉 MRI 显示双侧内收大肌均有多发性片状水肿,2 例均有不同大小的边缘不规则的空泡。病理表现包括肌纤维变性、弥漫性 MHC-I 阳性和细胞膜上补体沉积。在 1 例中发现了少数 RBF,而在 2 例中发现了弥漫性的内肌膜和肌周膜增生。

结论

AMA 阳性的炎性肌病是一种可影响多个系统的疾病。除了炎症改变外,肌肉的病理表现还可出现空泡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1f/10985968/7700f0179d25/12891_2023_6941_Fig1_HTML.jpg

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