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Solitary rhabdomyoma of the heart

Clinically silent case with sudden, unexpected death in an 11-month-old boy

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Abstract

We report a case of cardiac rhabdomyoma leading to sudden, unexpected death in an 11-monthold child.

Autopsy disclosed a firm nodular tumor located in the anterior part of the interventricular septum and anterior wall of the left chamber. The tumor bulged into the cavity of the left ventricle and caused appreciable narrowing of the outflow tract. Histologically, the typical “spider cells” characteristic for cardiac rhabdomyoma could be found. Sections cut from alcohol-fixed tissues and stained in water-free PAS showed that these cells contained massive amounts of a diastase-digestible PAS-positive material, presumably glycogen.

No evidence of tuberous sclerosis was detected. Sudden death was attributed to cardiac arrest due to irritation of the conducting system by the tumor.

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Authors and Affiliations

  1. Department of Pathology, University of Freiburg, Albertstraße 19, D-7800, Freiburg, Federal Republic of Germany

    N. Böhm & G. Krebs

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  1. N. Böhm
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  2. G. Krebs
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Böhm, N., Krebs, G. Solitary rhabdomyoma of the heart. Eur J Pediatr 134, 167–172 (1980). https://doi.org/10.1007/BF01846040

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  • DOI: https://doi.org/10.1007/BF01846040

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