Inflammatory myopathies in a patient with Darier\'s disease, a possible association

Authors

  • Abbas Darjani Department of Dermatology, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
  • Hojat Eftekhari Department of Dermatology, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
  • Kaveh Gharaeinejad Department of Dermatology, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
  • Narges Alizadeh Department of Dermatology, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
  • rana rafiei Department of Dermatology, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
Abstract:

Background: Darier disease (DD) is an autosomal dominant genetic disorder which develops from a mutation in the ATP2A2 gene. Inflammatory myopathies (IM) are the largest group of potentially treatable myopathies. In this case, we report development of IM in a patient with DD for the second time in the literature. Case presentation: The patient is a 59-year-old female, a known case of  DD, who developed proximal muscle weakness 2 weeks prior to admission. Elevated muscle-enzymes, as well as typical electromyographic and radiologic confirmed the diagnosis of IM. Conclusions: Abnormalities in intracellular calcium homeostasis may explain the association between DM and DD, therefore it is noteworthy to keep this association in mind and conduct more research regarding this issue

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Journal title

volume 9  issue None

pages  201- 203

publication date 2018-01

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