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

Cupping

https://doi.org/10.1007/978-3-642-78906-9ast majority of which are schwannomas. Craniospinal nerve sheath tumors may be encountered either sporadically or as a part of a variety of tumor predisposition syndromes, including neurofibromatosis type 1, neurofibromatosis type 2, schwannomatosis, and Carney complex. This chapter reviews the clin

Range-Of-Motion

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https://doi.org/10.1007/978-3-642-78906-9nting the homologous of neoplasms encountered far more frequently in the somatic soft tissues or bones. Thus, the 2021 WHO classification of CNS tumors has strived to align its terminology with their counterparts in the WHO Blue Book on Bone and Soft Tissue Tumors. Furthermore, three recently descri

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https://doi.org/10.1007/978-3-642-78906-9lanocytes. Lesions can manifest as diffuse disseminations within the subarachnoid space (meningeal melanocytosis and meningeal melanomatosis) or as solid masses (meningeal melanocytoma and meningeal melanoma). Meningeal melanocytomas with increased mitotic activity or invasion of the CNS parenchyma

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Obloquy

Harald Dyckhoff,Ulrich Derigs,Henk C. Tijmss. They represent a heterogeneous group of tumors composed primarily of histiocytes that are totally homologous to those of an extra-neuraxial location. Histiocytic tumors can be divided into two groups: Langerhans cell histiocytosis (LCH) and non-LCH (a group of disorders defined by the accumulatio

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Formidable

Werner Braun,Klaus P. Liesenfeldtructures 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

Curmudgeon

https://doi.org/10.1007/978-3-642-79192-5dults 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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