Your browser doesn't support javascript.
loading
Presentation of a Hemangioblastoma in cavernous sinus: An extremely rare case report.
Tabibkhooei, A; Fattahi, A; Rahatlou, H.
Afiliação
  • Tabibkhooei A; Neurosurgery, Iran University of Medical Sciences, Tehran, Iran. Electronic address: alireza.tabibkhooei@gmail.com.
  • Fattahi A; Neurosurgery, Iran University of Medical Sciences, Tehran, Iran. Electronic address: fatahi.a@iums.ac.ir.
  • Rahatlou H; Neurosurgery, Iran University of Medical Sciences, Tehran, Iran. Electronic address: dr.h.rahatlou@gmail.com.
Int J Surg Case Rep ; 44: 54-56, 2018.
Article em En | MEDLINE | ID: mdl-29477104
ABSTRACT

INTRODUCTION:

Hemangioblastoma (HB) is a benign vascular tumor that accounts for about 2% of intracranial neoplasms. HB of the cavernous sinus (CS) is extremely rare. Only one report was found in the literature. PRESENTATION OF CASE We present a 29-year-old female with progressive headache and she had right ptosis and right mild oculomotor nerve palsy. The brain Magnetic Resonance Imaging (MRI) revealed a right extra-axial 4 × 4 cm in right CS position. The patient was operated upon microscopically via sub-temporal approach through a right temporal craniotomy. After the subtotal removal of a highly vascular tumor, the patient was referred for adjuvant therapy with Gamma-knife surgery.

DISCUSSION:

Surgical removal of HB is the most effective treatment of the central nervous system (CNS) HBs. Tumors invading the CS could cause severe bleeding during surgery and HB-because of its vascular origin-had more risk for severe intraoperative bleeding, and in some cases resulted in surgery stop with subtotal resection of tumor.

CONCLUSION:

It was recommended to perform a pre-operative brain angiography and selective embolization of these highly vascular lesions that it could result in subsequent complete surgical removal.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2018 Tipo de documento: Article