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CASE REPORT
Pleomorphic rhabdomyosarcoma of the cerebellopontine angle in an adult: a review of literature
  1. Federico Caporlingua1,
  2. Gennaro Lapadula1,
  3. Manila Antonelli2,
  4. Paolo Missori1
  1. 1Department of Neurology and Psychiatry, Neurosurgery, “Sapienza” University of Rome, Rome, Italy
  2. 2Department of Pathology, “Sapienza” University of Rome, Rome, Italy
  1. Correspondence to Dr Federico Caporlingua, capor51{at}gmail.com

Summary

Rhabdomyosarcoma (RMS) is a rare and aggressive neoplasm characterised by rapid growth and metastatic invasion. The most frequent localisation is the skeletal musculature of the limbs. The head and the neck are rarely involved. A 50-year-old woman presented to our attention because of a progressively increasing headache, ataxia and vomiting. MRI showed a lesion at the right cerebellopontine angle. Thereafter, the patient was submitted to a piece-meal removal of the neoplasm. Despite the postoperative MRI showed no signs of remnant, 7 months after the surgery, the disease recurred with multiple localisations, and the patient died a few days later. This report is the first description in the literature of a pleomorphic RMS of the cerebellopontine angle. This particular tumour carries a bad prognosis because of the vicinity of nervous structures and of the impossibility of achieving a one-piece resection. More than ever, the adjunctive treatments had to be effective against a potential remnant and in controlling recurrences.

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