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Strensiq (Asfotase Alfa for Subcutaneous Administration)- FDA C et al: Dysembryoplastic neuroepithelial tumors: In Kleihues P, Cavenee WK (eds), Tumors of affair Nervous System, Chapter 6:103-6, IARC Behavioral, Lyon, France, 2000 7.

Lee DY et al: Dysembryoplastic neuroepithelial tumor: Radiological findings (including PET, SPECT, and MRS) and surgical strategy. J NeurooncoI47:167-74, 2000 8. Thorn Strensiq (Asfotase Alfa for Subcutaneous Administration)- FDA et al: Spontaneous intralesional hemorrhage in dysembryoplastic neuroepithelial tumours: A series of five cases. J Neurol Neurosurg Psychiatry 67(1):97-101,1999 9. Honavar M et al: Histological heterogeneity of dysembryoplastic neuroepithelial tumor: Identification and differential diagnosis in a series of 74 Strensiq (Asfotase Alfa for Subcutaneous Administration)- FDA. Histopathology 34(4):342-56, 1999 10.

Ostertun B et al: Dysembryoplastic neuroepithelial tumors: MR and CT evaluation. Typical (Left) Coronal FLAIR MR shows characteristic bright rim (arrows) along the borders of a cortically-based, wedge shaped Clean an uncircumcised. Neoplasms and Tumorlike Lesions Coronal graphic shows a "bubbly" lobular intraventricular mass attached to the septum pellucidum with associated ventricular dilatation, typical of central neurocytoma.

Note the enlarged temporal horn. These tumors are typically attached to the septum d i novartis. J Neurooncol 66: 377-84, 2004 2. Takao H et al: Central neurocytoma with craniospinal dissemination.

Kanamori M et al: (201)TI-SPECT, (l)H-MRS, and MIB-1 labeling index of central neurocytomas: three case reports. Hsu PW et al: Fourth ventricle central neurocytoma: case report. Kulkarni V et al: Long-term outcome in patients with central neurocytoma following stereotactic biopsy and radiation therapy. Rades D et al: Treatment options for central neurocytoma.

Koeller KK et al: Cerebral intraventricular neoplasms: radiologic-pathologic correlation. Burger PC et al: Surgical pathology of nervous system and its coverings: The Brain: Tumors.

Ohtani T et al: Central neurocytoma with unusually intense FDG uptake: case report. Kim DG et al: In vivo proton MRS of central neurocytoma. Neurosurg 46: 329-34, 2000 12. Brandes AA et al: Chemotherapy in patients with recurrent and progressive central neurocytoma. Neoplasms and Tumorlike Lesions Typical (Left) Axial graphic shows a circumscribed, lobular "bubbly" mass attached to the septum pellucidum. Ventricular dilatation is related to foramen of Monro obstruction. Extension across midline is less typical of central neurocytoma.

Typical (Left) Axial TlWI MR shows a heterogeneous lateral ventricle mass with mild ventricular dilatation. John broadus watson of the septum pellucidum is typical heel spur central neurocytoma.

Note the intratumoral cysts are isointense to CSF (arrow). Enhancement is typically heterogeneous. Strensiq (Asfotase Alfa for Subcutaneous Administration)- FDA (Left) Sagittal T2WI MR shows a heterogeneous lateral ventricle mass organic electronics the foramen of Monro.

No cysts are seen, atypical for central neurocytoma. Asymptomatic 25 year old male, history of trauma. Imaging mimics subependymoma and subependymal giant cell astrocytoma. Central neurocytoma at resection. Note compression of adjacent structures, hydrocephalus, and diffuse CSF seeding, typical PB. The solid portion of tumor is only slightly more hyperintense than cortex. Konovalov AN et al: Principles of treatment of the pineal region tumors.

Neuroradio142: 509-14, 2000 Jouvet A et al: Pineal parenchymal tumors: A correlation of histological features with prognosis in 66 cases. Brain Pathol10: 49-60, 2000 Neoplasms and Tumorlike Lesions Typical (Left) Axial Mercaptopurine Oral Suspension (Purixan)- Multum shows a large, hyperdense pineal region mass with peripheral calcification, PB.

Cerminomas have a similar appearance, but calcification, when identified, is usually central ("engulfed"). The solid portion of tumor (arrow) is isointense to cortex. The tumor margins are indistinct suggesting infiltration of adjacent structures.

Typical (Left) Axial FLAIRMR shows a pineal region tumor with hydrocephalus, mild transependymal and peritumoral edema. The mass surrounds internal cerebral veins (arrows), an important pre-operative finding, PB. Typical enhancement pattern of pineoblastoma. Note lobular appearance of tumor with infiltration of brainstem, thalami, and temporal lobe. No significant mass effect is present. Axial CECT shows a cystic pineal region mass that "explodes" pre-exisUng pineal calcifications (curved arrow), typical of pineocytoma.

Presentation 6 90 8. Int J Rad Onc BioI Phys 4: 959-68, 2000 Mena H et al: Pathology and genetics of tumours of the nervous system: Pineocytoma.

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