Literature DB >> 19900728

Left ventricular hypertrabeculation/noncompaction in hereditary inclusion body myopathy.

Josef Finsterer, Claudia Stöllberger, Romana Höftberger.   

Abstract

Left ventricular hypertrabeculation (LVHT) also known as noncompaction has not been reported in association with hereditary inclusion body myopathy (IBM). In a 62 year old Caucasian male, with a history of muscle stiffness, myalgias, recurrent hyper-creatin-kinase(CK)-aemia, muscle cramps particularly during cold, polyarthralgias, a family history positive for muscle cramping and muscle disease, normal clinical neurologic examination, and myogenic needle EMG, muscle biopsy was indicative of hereditary IBM. Cardiologic investigations revealed arterial hypertension, left anterior hemiblock, slight myocardial thickening, and surprisingly lone LVHT. LVHT was not associated with arrhythmias, systolic dysfunction, or cardioembolic events, No neurological or cardiac therapy was necessary. During a follow-up of 18 months neither the neurological nor the cardiologic abnormalities progressed. LVHT may also occur in patients with IBM. Patients with hereditary IBM should be investigated for cardiac involvement, which may manifest not only as myocardial damage but also as impulse propagation abnormalities.
Copyright © 2009 Elsevier Ireland Ltd. All rights reserved.

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Year:  2009        PMID: 19900728     DOI: 10.1016/j.ijcard.2009.10.017

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  2 in total

Review 1.  Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors.

Authors:  Josef Finsterer; Claudia Stöllberger; Jeffrey A Towbin
Journal:  Nat Rev Cardiol       Date:  2017-01-12       Impact factor: 32.419

Review 2.  Unclassified cardiomyopathies in neuromuscular disorders.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Wien Med Wochenschr       Date:  2013-10-24
  2 in total

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