Choroid plexus carcinoma: report of one case with favourable response to treatment

Med Pediatr Oncol. 1994;22(4):274-8. doi: 10.1002/mpo.2950220412.

Abstract

Choroid plexus carcinoma (CPC) is a rare tumor with usually severe prognosis, whose optimal treatment has not yet been established. The exact role of complete surgical resection, chemotherapy, and radiotherapy has been debated but not clarified. We report one girl with CPC diagnosed at age 3 months and apparently cured with minimal surgical resection, chemotherapy, and delayed irradiation. At the age of 8 years, she is well, with minor psychomotor retardation and growth hormone deficiency as the only sequelae.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Carcinoma, Papillary / diagnosis
  • Carcinoma, Papillary / pathology
  • Carcinoma, Papillary / therapy*
  • Choroid Plexus Neoplasms / diagnosis
  • Choroid Plexus Neoplasms / pathology
  • Choroid Plexus Neoplasms / therapy*
  • Combined Modality Therapy
  • Female
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Prognosis
  • Tomography, X-Ray Computed