Myoglobinuria in two patients with Duchenne muscular dystrophy after treatment with zoledronate: a case-report and call for caution

被引:10
|
作者
Ivanyuk, Anton [1 ]
Segarra, Nuria Garcia [2 ]
Buclin, Thierry [1 ]
Klein, Andrea [3 ,4 ,5 ]
Jacquier, David [3 ]
Newman, Christopher J. [3 ]
Bloetzer, Clemens [3 ,6 ]
机构
[1] CHU Vaudois, Serv Clin Pharmacol, Lausanne Univ Hosp, Bugnon 17, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Ctr Mol Dis, Lausanne Univ Hosp, Div Genet Med, Pierre Decker 2, CH-1011 Lausanne, Switzerland
[3] CHU Vaudois, Paediat Neurol & Neurorehabil Unit, Lausanne Univ Hosp, Pierre Decker 5, CH-1011 Lausanne, Switzerland
[4] UKBB, Pediat Neurol, Univ Childrens Hosp Basel, Basel, Switzerland
[5] Inselspital Bern, Bern, Switzerland
[6] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
关键词
Duchenne muscular dystrophy; myoglobinuria; bisphosphonates; zoledronate; BISPHOSPHONATE THERAPY; DOUBLE-BLIND; OSTEOPOROSIS; RHABDOMYOLYSIS; ALENDRONATE; CHILDREN; BOYS;
D O I
10.1016/j.nmd.2018.08.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rhabdomyolysis with myoglobinuria is a recognized complication of dystrophinopathies. It can be triggered by infections, exercise or volatile anesthetics. To our knowledge, it has never been reported in boys with Duchenne muscular dystrophy (DMD) after the administration of bisphosphonates. We report two patients with DMD who presented an apparent transient rhabdomyolysis with myoglobinuria after zoledronate administration. Possible mechanisms could involve hypophosphatemia, a known dose-dependent side effect of bisphosphonates, and/or direct myotoxicity of biphosphonates. Physicians and families should be aware of rhabdomyolysis with myoglobinuria as a potential uncommon side effect of bisphosphonates in DMD, in particular of zoledronate. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:865 / 867
页数:3
相关论文
共 50 条
  • [31] Duchenne muscular dystrophy involves the myocardium and causes arrhythmia: Case report
    Liu, Xuhan
    Zhao, Wei
    Shu, Shangzhi
    Zhang, Weihua
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 9
  • [32] Evaluation of Serial Casting for Boys with Duchenne Muscular Dystrophy: A Case Report
    Carroll, Kate
    de Valle, Katy
    Kornberg, Andrew
    Ryan, Monique
    Kennedy, Rachel
    PHYSICAL & OCCUPATIONAL THERAPY IN PEDIATRICS, 2018, 38 (01) : 88 - 96
  • [33] Coexisting Duchenne Muscular Dystrophy and Gilbert's Syndrome: A Case Report
    Incecik, Faruk
    Herguner, M. Ozlem
    Mert, Gulen
    Horoz, Ozden
    Altunbasak, Sakir
    CUKUROVA MEDICAL JOURNAL, 2013, 38 (04): : 791 - 793
  • [34] Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East
    Alghamdi, Fouad
    Al-Tawari, Asmaa
    Alrohaif, Hadil
    Alshuaibi, Walaa
    Mansour, Hicham
    Aartsma-Rus, Annemieke
    Megarbane, Andre
    FRONTIERS IN PEDIATRICS, 2021, 9
  • [35] Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports
    Nozoe, Karen T.
    Akamine, RicardoT.
    Mazzotti, Diego R.
    Polesel, Daniel N.
    Grossklauss, Luis F.
    Tufik, Sergio
    Andersen, Monica L.
    Moreira, Gustavo A.
    SLEEP SCIENCE, 2016, 9 (03) : 129 - 133
  • [36] A SYMPTOMATIC FEMALE-PATIENT WITH DUCHENNE MUSCULAR-DYSTROPHY DIAGNOSED BY DYSTROPHIN-STAINING - A CASE-REPORT
    SHIGIHARAYASUDA, K
    TONOKI, H
    GOTO, Y
    ARAHATA, K
    ISHIKAWA, N
    KAJII, N
    FUJIEDA, K
    EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (01) : 66 - 68
  • [37] Effect on bone remodelling after vibration treatment in Duchenne muscular dystrophy
    Soderpalm, A. -C.
    Magnusson, P.
    Kroksmark, A. -K.
    Karlsson, J.
    Tulinius, M.
    Swolin-Eide, D.
    BONE, 2012, 50 : S191 - S192
  • [38] Immune status changes of patients with Duchenne Muscular Dystrophy after the embryonic allogenic myoblasts treatment
    Tsymbalyuk, Vitalyi
    Pichkur, Leonid
    Pichkur, Natalyia
    Markova, Olga
    NEUROMUSCULAR DISORDERS, 2006, 16 : S186 - S186
  • [39] Expression of Dystrophin in Duchenne Muscular Dystrophy Patients after Myoblast Transplantation
    S. S. Shishkin
    S. M. Terekhov
    T. B. Krokhina
    N. I. Shakhovskaya
    A. N. Podobedova
    G. F. Lyannaya
    V. I. Tarasov
    V. I. Ovchinnikov
    I. N. Krakhmaleva
    S. F. Zakharov
    E. S. Ershova
    S. A. Limborska
    T. V. Pogoda
    E. A. Zotikov
    P. M. Kut'ina
    M. A. Tarksh
    V. S. Sukhorukov
    N. L. Gerasimova
    Russian Journal of Genetics, 2001, 37 : 919 - 925
  • [40] Longevity after spinal surgery in patients with Duchenne Muscular Dystrophy.
    Singer, MN
    Worthington, DJ
    PEDIATRICS, 1998, 102 (03) : 742 - 743