Choroid plexus carcinoma in adults: an extremely rare case


Ozdogan S., Gergin Y. E., Gergin S., Senol O., Tiryaki M., Tatarli N., ...Daha Fazla

PAN AFRICAN MEDICAL JOURNAL, cilt.20, 2015 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 20
  • Basım Tarihi: 2015
  • Doi Numarası: 10.11604/pamj.2015.20.302.5854
  • Dergi Adı: PAN AFRICAN MEDICAL JOURNAL
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus
  • Anahtar Kelimeler: Choroid plexus tumors, Choroid plexus carcinomas, Choroid plexus neoplasms in adults
  • Marmara Üniversitesi Adresli: Evet

Özet

Choroid plexus tumors are rare intraventricular papillary neoplasms derived from choroid plexus epithelium, which account for approximately 2% to 4% of intracranial tumors in children and 0.5% in adults. Almost all choroid plexus carcinomas are seen in children and are extremely rare in adults. Headache, diplopia, and ataxia are the most common symptoms usually caused by mechanical obstruction of cerebrospinal fluid flow followed by hydrocephalus, regardless of tumor location. We present an illustrative case with 73 years old male patient who was consulted with headache to our neurosurgery department. In cranial computed tomography, there was a mass in 4th ventricle and we confirmed the mass with magnetic resonance imaging. After surgery had been performed, pathology specimen was diagnosed as choroid plexus carcinoma which was rarely seen in this age group.