Titlebook: Central Nervous System Tumors; Diagnostic Pathology César R. Lacruz Book 2023 The Editor(s) (if applicable) and The Author(s), under exclus

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Tumors of the Sellar Region,tructures converges. This is way this region can host such a numerous and heterogeneous group of neoplasms (Table .). This chapter will focus on updates for ., ., ., . (pituicytoma, granular cell tumor of the sellar region, spindle cell oncocytoma, sellar ependymoma), and . as well as discuss other

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Metastases to the CNS and Its Coverings,dults and about 2% in children. Recent advances in the management of patients with CNS metastases have made accurate diagnosis of these tumors of paramount importance. This chapter reviews the epidemiology; topography; clinicoradiologic features; diagnostic criteria—including ancillary studies—; and

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Circumscribed Astrocytic Gliomas, is generally more favorable than the adult-type diffuse gliomas, being attempt of gross total resection the treatment of choice. This chapter reviews the clinicopathologic features and differential diagnosis of these entities as well as of their subtypes.

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Cranial and Paraspinal Nerve Tumors,icopathological features and differential diagnosis of schwannoma, neurofibroma, malignant melanotic nerve sheath tumor (previously melanotic schwannoma), malignant peripheral nerve sheath tumor, cauda equina neuroendocrine tumor (previously spinal paraganglioma), and ganglioneuroma.

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Primary CNS Lymphomas,standing of the etiology and pathogenesis of primary CNS lymphomas, the mainstay of their diagnostic assessment remains tissue-based classification using histological and immunohistochemical analysis of biopsy specimens. This chapter reviews the clinicopathological features and differential diagnosis of all these entities.

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Pineal Tumors,xclusively in this specific localization. This chapter will focus on updates for pineal parenchymal tumors; papillary tumor of the pineal region; desmoplastic myxoid tumor of the pineal region, SMARCB1-mutant; and pineal anlage tumor.

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3-D-Rekonstruktion bei Azetabulumfrakturenasic types: astrocytoma, IDH-mutant (CNS WHO grades 2, 3, 4); oligodendroglioma, IDH-mutant and 1p/19q-codeleted (CNS WHO grades 2, 3); and glioblastoma, IDH-wildtype (CNS WHO grade 4). This chapter reviews the clinicopathologic features and differential diagnosis of these entities as well as of their subtypes.

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