Intraparenchymal Schwannoma of Temporal Lobe: A Case Report and Review of the Literature.
Sajjad SaghebdoustMohammad Amin HabibiMehran EkramiFarshid KhadivarMohammad Moein VakilzadehReza ZarePublished in: Asian journal of neurosurgery (2023)
Intracranial schwannomas (ISs) account for approximately 8% of intracranial tumors, while IS, a rare entity, is responsible for roughly 1% of IS. A 33-year-old man with a 3-month headache and sudden onset seizure was referred to our clinic. Preoperative magnetic resonance imaging revealed a contrast-enhancing mass accompanied by cystic components in the right temporal lobe. Ganglioglioma, metastasis, or glioblastoma multiforme was suspected, and surgery was advised. During surgery, gross total resection of a noninvasive tumor was conducted. Postoperative recovery was uneventful. Based on histopathological examination and confirmatory immunohistochemistry, the intraparenchymal temporal tumor was diagnosed as schwannoma. ISs are extremely scarce brain tumors mainly located on the surface of the brain or adjacent brain ventricles. The definite preoperative diagnosis of schwannoma cannot be readily established due to radiologically indistinguishable features from metastasis and gliomas; however, histopathology and immunohistochemistry are of great assistance. Complete surgical removal is the most preferred treatment alternative with a long-term favorable prognosis without adjuvant and neoadjuvant chemotherapy requirements.
Keyphrases
- neoadjuvant chemotherapy
- minimally invasive
- patients undergoing
- magnetic resonance imaging
- coronary artery bypass
- locally advanced
- white matter
- resting state
- sentinel lymph node
- lymph node
- contrast enhanced
- primary care
- early stage
- surgical site infection
- magnetic resonance
- pulmonary embolism
- computed tomography
- cerebral ischemia
- optic nerve
- squamous cell carcinoma
- radiation therapy
- functional connectivity
- rectal cancer
- children with cerebral palsy
- temporal lobe epilepsy