| Literature DB >> 19162348 |
Pasquale Santangeli, Maurizio Pieroni, Francesca Marzo, Antonio Frontera, Nicola Vitulano, Nicola Luciani, Fulvio Bellocci, Filippo Crea.
Abstract
A 51-year-old man was admitted for burning dysesthesias over the soles. Neurologic examination showed a pansensory loss over both feet associated with weakness of toes dorsiflexion. Motor conduction study of the sural nerve showed a significant reduction of nerve conduction velocity (21.4 m/s) suggesting a demyelinating neuropathy. In the following days he was referred to the cardiologist because of the sudden onset of a rapid atrial tachycardia, which was terminated by adenosine. Echocardiography showed a left atrial mass arising from the atrial septum consistent with the diagnosis of cardiac myxoma. The patient underwent cardiac surgery to remove the tumor, which was confirmed a myxoma by pathology. In the days following cardiac mass removal, neurological symptoms progressively disappeared in the absence of anti-inflammatory and steroid therapy and control motor conduction study showed complete normalization of nerve conduction velocity (54.5 m/s). Peripheral demyelinating neuropathy represented the first clinical presentation of cardiac myxoma in our patient and should be included among the possible paraneoplastic manifestations of this cardiac tumor. Copyright (c) 2008 Elsevier Ireland Ltd. All rights reserved.Entities:
Mesh:
Year: 2009 PMID: 19162348 DOI: 10.1016/j.ijcard.2008.12.038
Source DB: PubMed Journal: Int J Cardiol ISSN: 0167-5273 Impact factor: 4.164