Severe rhabdomyolysis after MIHA-bodytec® electrostimulation with previous mild hyper-CK-emia and noncompaction

International Journal of Cardiology

Volumn 180, Issue , 2015, Pages 100-102

  Finsterer, Josef ^a   Stöllberger, Claudia ^a  

^a KRANKENANSTALT RUDOLFSTIFTUNG   (Austria)

Author keywords

Cardiomyopathy; Metabolic myopathy; Muscle aching; Non compaction; Rhabdomyolysis

Indexed keywords

CLENBUTEROL; CREATINE KINASE; 16-IODO-3-METHYLHEXADECANOIC ACID; PALMITIC ACID DERIVATIVE; RADIOACTIVE IODINE;

ADULT; CASE REPORT; CREATINE KINASE BLOOD LEVEL; DISEASE SEVERITY; ECHOCARDIOGRAPHY; ELECTROCONVULSIVE THERAPY; ELECTROMYOGRAPHY; ELECTRONEUROGRAPHY; ELECTROSTIMULATION; FEMALE; FITNESS; HOUSEHOLD; HUMAN; LETTER; MEDICAL DEVICE; MUSCLE CRAMP; MUSCLE EXAMINATION; MUSCLE TRAINING; MYALGIA; NEUROLOGIC EXAMINATION; RHABDOMYOLYSIS; TRANSTHORACIC ECHOCARDIOGRAPHY; VENTRICULAR NONCOMPACTION; ADVERSE EFFECTS; BLOOD; COMPLICATION; PROCEDURES; SEVERITY OF ILLNESS INDEX; TRANSCUTANEOUS NERVE STIMULATION;

ADULT; CREATINE KINASE; FEMALE; HUMANS; IODINE RADIOISOTOPES; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; PALMITIC ACIDS; RHABDOMYOLYSIS; SEVERITY OF ILLNESS INDEX; TRANSCUTANEOUS ELECTRIC NERVE STIMULATION;

EID: 84920517887     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2014.11.148     Document Type: Article

References (34)

1. G. Terrone, M. Ruoppolo, N. Brunetti-Pierri, C. Cozzolino, E. Scolamiero, G. Parenti, A. Romano, G. Andria, F. Salvatore, and G. Frisso Child neurology: recurrent rhabdomyolysis due to a fatty acid oxidation disorder Neurology 82 2014 e1 e4
2. E.J. Giltay, K.H. Kho, and B.A. Blansjaar Serum markers of brain-cell damage and C-reactive protein are unaffected by electroconvulsive therapy World J. Biol. Psychiatry 9 2008 231 235
3. R. Quinlivan, and H. Jungbluth Myopathic causes of exercise intolerance with rhabdomyolysis Dev. Med. Child Neurol. 54 2012 886 891
4. P. Lehmann, W. Hartung, and M. Fleck Rhabdomyolysis and creatine kinase elevation Z. Rheumatol. 72 2013 236 241
5. T.O. Cheng Left ventricular noncompaction cardiomyopathy: three decades of progress Int. J. Cardiol. 174 2014 227 229
6. G. Molinari, A. Valbusa, and S. Domenicucci Isolated noncompaction of the left ventricular myocardium and intraventricular thrombosis detected by magnetic resonance imaging Int. J. Cardiol. 168 2013 e123 e124
7. J. Finsterer, C. Stöllberger, O. Brandau, F. Laccone, K. Bichler, and N.G. Laing Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction Int. J. Cardiol. 173 2014 532 535
8. D. Gerger, C. Stöllberger, M. Grassberger, B. Gerecke, H. Andresen, R. Engberding, and J. Finsterer Pathomorphologic findings in left ventricular hypertrabeculation/noncompaction of adults in relation to neuromuscular disorders Int. J. Cardiol. 169 2013 249 253
9. R.S. Simpson, and K. Van Fatal rhabdomyolysis following volatile induction in a six-year-old boy with Duchenne muscular dystrophy Anaesth. Intensive Care 41 2013 805 807
10. P. Ambrosi, A. Mouly-Bandini, S. Attarian, and G. Habib Heart transplantation in 7 patients from a single family with limb-girdle muscular dystrophy caused by lamin A/C mutation Int. J. Cardiol. 137 2009 e75 e76
11. K.D. Mathews, C.M. Stephan, K. Laubenthal, T.L. Winder, D.E. Michele, S.A. Moore, and K.P. Campbell Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I Neurology 76 2011 194 195
12. L. Pena, K. Kim, and J. Charrow Episodic myoglobinuria in a primary gamma-sarcoglycanopathy Neuromuscul. Disord. 20 2010 337 339
13. A. Aboumousa, J. Hoogendijk, R. Charlton, R. Barresi, R. Herrmann, T. Voit, J. Hudson, M. Roberts, D. Hilton-Jones, M. Eagle, K. Bushby, and V. Straub Caveolinopathy - new mutations and additional symptoms Neuromuscul. Disord. 18 2008 572 578
14. D. Ronchi, C. Garone, A. Bordoni, P. Gutierrez Rios, S.E. Calvo, M. Ripolone, M. Ranieri, M. Rizzuti, L. Villa, F. Magri, S. Corti, N. Bresolin, V.K. Mootha, M. Moggio, S. DiMauro, G.P. Comi, and M. Sciacco Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions Brain 135 2012 3404 3415
15. C.R. Vissing, M. Duno, J.H. Olesen, J. Rafiq, L. Risom, E. Christensen, F. Wibrand, and J. Vissing Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene Neurology 80 2013 1908 1910
16. D.I. Zafeiriou, A. Ververi, A. Tsitlakidou, A. Anastasiou, and E. Vargiami Recurrent episodes of rhabdomyolysis in pontocerebellar hypoplasia type 2 Neuromuscul. Disord. 23 2013 116 119
17. M. Alečković-Halilović, E. Mešić, O. Sinanović, S. Zukić, and J. Mustedanagić Carnitine palmitoyl transferase deficiency - unrecognized cause of recurrent acute kidney injury Ren. Fail. 35 2013 732 734
18. T. Liewluck, M.S. Mundi, and M.L. Mauermann Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis Muscle Nerve 48 2013 989 991
19. R. Izumi, N. Suzuki, M. Nagata, T. Hasegawa, Y. Abe, Y. Saito, H. Mochizuki, M. Tateyama, and M. Aoki A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure Intern. Med. 50 2011 2663 2668
20. T.F. Eminoglu, L. Tumer, I. Okur, F.S. Ezgu, G. Biberoglu, and A. Hasanoglu Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide Forensic Sci. Int. 210 2011 e1 e3
21. B.R. Keel, and M. Brit McArdle's disease: a clinical review and case report Tenn. Med. 106 2013 33 (37)
22. O. Musumeci, C. Bruno, T. Mongini, C. Rodolico, M. Aguennouz, E. Barca, A. Amati, D. Cassandrini, L. Serlenga, G. Vita, and A. Toscano Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII) Neuromuscul. Disord. 22 2012 325 330
23. E. Sotiriou, P. Greene, S. Krishna, M. Hirano, and S. DiMauro Myopathy and parkinsonism in phosphoglycerate kinase deficiency Muscle Nerve 41 2010 707 710
24. M. Castro-Gago, C. Gómez-Lado, L. Pérez-Gay, J. Eirís-Puñal, E.P. Martínez, I. García-Consuegra, and M.A. Martín Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant J. Child Neurol. 26 2011 734 737
25. M. Prasad, and S. Hussain Glutaric aciduria type II presenting as myopathy and rhabdomyolysis in a teenager J. Child Neurol. 2014 (in press)
26. E. Lee, and N. Chahin A patient with mutation in the SCN4A p.M1592v presenting with fixed weakness, rhabdomyolysis, and episodic worsening of weakness Muscle Nerve 48 2013 306 307
27. C. Michot, L. Hubert, N.B. Romero, A. Gouda, A. Mamoune, S. Mathew, E. Kirk, L. Viollet, S. Rahman, S. Bekri, H. Peters, J. McGill, E. Glamuzina, M. Farrar, M. von der Hagen, I.E. Alexander, B. Kirmse, M. Barth, P. Laforet, P. Benlian, A. Munnich, M. JeanPierre, O. Elpeleg, O. Pines, A. Delahodde, Y. de Keyzer, and P. de Lonlay Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia J. Inherit. Metab. Dis. 35 2012 1119 1128
28. M. Milone, T. Liewluck, T.L. Winder, and P.T. Pianosi Amyloidosis and exercise intolerance in ANO5 muscular dystrophy Neuromuscul. Disord. 22 2012 13 15
29. M. Davis, R. Brown, A. Dickson, H. Horton, D. James, N. Laing, R. Marston, M. Norgate, D. Perlman, N. Pollock, and K. Stowell Malignant hyperthermia associated with exercise-induced rhabdomyolysis or congenital abnormalities and a novel RYR1 mutation in New Zealand and Australian pedigrees Br. J. Anaesth. 88 2002 508 515
30. G. Esposito, L. Vitagliano, A. Cevenini, T. Amelio, A. Zagari, and F. Salvatore Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child Blood 105 2005 905 906
31. A. Carsana Exercise-induced rhabdomyolysis and stress-induced malignant hyperthermia events, association with malignant hyperthermia susceptibility, and RYR1 gene sequence variations Sci. World J. 2013 2013 531465 10.1155/2013/531465 (Epub 2013 Feb 10)
32. W.T. Tsai, Y.L. Chen, W.S. Yang, H.D. Lin, C.C. Chien, and C.L. Lin Primary aldosteronism associated with severe hypokalemic rhabdomyolysis Hormones (Athens) 11 2012 505 506
33. G. Kollberg, A. Melberg, E. Holme, and A. Oldfors Transient restoration of succinate dehydrogenase activity after rhabdomyolysis in iron-sulphur cluster deficiency myopathy Neuromuscul. Disord. 21 2011 115 120
34. M.S. Kim, C. Muratore, L. Snelling, D.E. Mandelbaum, R. McEachern, S. Mangray, M. Faizan, and J.B. Quintos Ischemic stroke and rhabdomyolysis in a 15-year-old girl with paraganglioma due to an SDHB exon 6 (Q214X) mutation J. Pediatr. Endocrinol. Metab. 22 2009 565 571