Skip Navigation LinksHome > May 2013 - Volume 35 - Issue 4 > Wilms Tumor Presenting With Lambert-Eaton Myasthenic Syndrom...
Journal of Pediatric Hematology/Oncology:
doi: 10.1097/MPH.0b013e31828d46a7
Original Articles

Wilms Tumor Presenting With Lambert-Eaton Myasthenic Syndrome

Petersen, Cheryl L. RN, BSN*; Hemker, Bradd G. MD; Jacobson, Richard D. MD, PhD; Warwick, Anne B. MD, MPH; Jaradeh, Safwan S. MD§; Kelly, Michael E. MD, PhD

Collapse Box

Abstract

Paraneoplastic syndromes may affect the central and peripheral nervous system of adults and children with cancer. Neurological symptoms may resolve with treatment of the underlying neoplasm. We report the case of a child with Wilms tumor who presented with generalized weakness, fatigue, ptosis, hypokinesis, dysarthria, urinary retention, facial diplegia, ophthalmoplegia, and autonomic dysfunction. Routine electrodiagnostic testing, including repetitive nerve stimulation, was normal. Clinical features and stimulation single-fiber electromyogram were consistent with a neuromuscular junction transmission disorder, likely Lambert-Eaton myasthenic syndrome. The child’s neurological status returned to normal with successful treatment of the tumor.

© 2013 Lippincott Williams & Wilkins, Inc.

Login

Article Tools

Share

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.

Connect With Us

Twitter
twitter.com/JPHOonline

For additional oncology content, visit LWW Oncology Journals on Facebook.