Muscle weakness and CK elevation: is it myositis?

被引:0
作者
Kernder, A. [1 ]
Mucke, J. [1 ]
Moldova, A-S [2 ]
Albrecht, P. [2 ]
Neuen-Jacob, E. [3 ]
Schneider, M. [1 ]
机构
[1] Univ Klinikum Dusseldorf, Poliklin Rheumatol & Hiller Forschungszentrum, Moorenstr 5, D-40225 Dusseldorf, Germany
[2] Univ Klinikum Dusseldorf, Klin Neurol, Dusseldorf, Germany
[3] Univ Klinikum Dusseldorf, Inst Neuropathol, Dusseldorf, Germany
来源
ZEITSCHRIFT FUR RHEUMATOLOGIE | 2020年 / 79卷 / 06期
关键词
Myopathy; Creatine kinase; Muscle biopsy; HMG-CoA reductase antibodies; Immune-mediated necrotizing myopathie (IMNM); MYOADENYLATE DEAMINASE DEFICIENCY; THERAPY;
D O I
10.1007/s00393-020-00815-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatologists are often confronted by patients with muscle weakness and elevated creatine kinase (CK) levels. Myositis cannot always be determined to be the cause of the complaints. This article presents two cases from our hospital where the diagnosis could only be determined by muscle biopsy. In the first case the patient presented with muscle weakness, pathological weight loss and a significant increase in CK levels. A muscle biopsy revealed an immune-mediated necrotizing myopathy (IMNM) caused by anti-3-hydroxy-3-methyl-gulatryl-CoA reductase (HMG-CoA reductase) autoantibodies due to the intake of statins. The second patient presented with cramp-like and burning muscle pain and weakness of the extremities without a relevant increase in CK level. Myoadenylate deaminase deficiency was also detected by muscle biopsy, and further confirmed by genetic testing.
引用
收藏
页码:578 / 583
页数:6
相关论文
共 17 条
[1]   Myopathy with anti-HMGCR antibodies Perimysium and myofiber pathology [J].
Alshehri, Ali ;
Choksi, Ran ;
Bucelli, Robert ;
Pestronk, Alan .
NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION, 2015, 2 (04)
[2]   Pathogenic Role of Anti-Signal Recognition Protein and Anti-3-Hydroxy-3-Methylglutaryl-CoA Reductase Antibodies in Necrotizing Myopathies: Myofiber Atrophy and Impairment of Muscle Regeneration in Necrotizing Autoimmune Myopathies [J].
Arouche-Delaperche, Louiza ;
Allenbach, Yves ;
Amelin, Damien ;
Preusse, Corinna ;
Mouly, Vincent ;
Mauhin, Wladimir ;
Tchoupou, Gaelle Dzangue ;
Drouot, Laurent ;
Boyer, Olivier ;
Stenzel, Werner ;
Butler-Browne, Gillian ;
Benveniste, Olivier .
ANNALS OF NEUROLOGY, 2017, 81 (04) :538-548
[3]   "Therapy-resistant polymyositis" - is the diagnosis correct? [J].
Ceccon, G. ;
Lehmann, H. C. ;
Neuen-Jacob, E. ;
Meng, G. ;
Fink, G. R. ;
Wunderlich, G. .
ZEITSCHRIFT FUR RHEUMATOLOGIE, 2017, 76 (07) :640-643
[4]   The composition of cellular infiltrates in anti-HMG-CoA reductase-associated myopathy [J].
Chung, Tae ;
Christopher-Stine, Lisa ;
Paik, Julie J. ;
Corse, Andrea ;
Mammen, Andrew L. .
MUSCLE & NERVE, 2015, 52 (02) :189-195
[5]  
Deschauer M, 2016, S1 LEITLINIE DIAGNOS
[6]   MYOADENYLATE DEAMINASE DEFICIENCY - INHERITED AND ACQUIRED FORMS [J].
FISHBEIN, WN .
BIOCHEMICAL MEDICINE, 1985, 33 (02) :158-169
[7]   A novel bipartite intronic splicing enhancer promotes the inclusion of a mini-exon in the AMP deaminase 1 gene [J].
Genetta, T ;
Morisaki, H ;
Morisaki, T ;
Holmes, EW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) :25589-25597
[8]   IMMUNE-MEDIATED NECROTIZING MYOPATHY ASSOCIATED WITH STATINS [J].
Grable-Esposito, Phyllis ;
Katzberg, Hans D. ;
Greenberg, Steven A. ;
Srinivasan, Jayashri ;
Katz, Jonathan ;
Amato, Anthony A. .
MUSCLE & NERVE, 2010, 41 (02) :185-190
[9]   METABOLISM OF D-RIBOSE ADMINISTERED CONTINUOUSLY TO HEALTHY-PERSONS AND TO PATIENTS WITH MYOADENYLATE DEAMINASE DEFICIENCY [J].
GROSS, M ;
REITER, S ;
ZOLLNER, N .
KLINISCHE WOCHENSCHRIFT, 1989, 67 (23) :1205-1213
[10]   Statin-Associated Autoimmune Myopathy [J].
Mammen, Andrew L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (07) :664-669