B.K. Kleinschmidt-DeMasters,
B.K., MD (Professor of Pathology, Neurology, and Neurosurgery, Director of Neuropathology, University of Colorado School of Medicine, Aurora, Colorado) Kleinschmidt-DeMasters,
Melike Pekmezci,
Melike, MD (Melike Pekmezci, MD, Associate Professor of Pathology and Ophthalmology, Department of Pathology and Ophthalmology, University of California, San Francisco; Staff Pathologist, San Francisco Veterans Affairs Medical Center, San Francisco, Calif,
Fausto Rodriguez,
Fausto, MD (Professor and Chief of Neuropathology, David Geffen School of Medicine, Department of Pathology and Laboratory Medicine, University of California, Los Angeles, Los Angeles, California) Rodriguez,
Tarik Tihan,
Tarik, MD, PhD (Professor of Pathology, Neuropathology Division, University of California San Francisco School of Medicine, San Francisco, California) Tihan
e.a.
Elsevier Health Sciences
e druk, 2022
9780323713306
Diagnostic Pathology: Neuropathology
Specificaties
Gebonden, blz.
|
Engels
Elsevier Health Sciences |
2022
ISBN13: 9780323713306
Rubricering
Onderdeel van serie
Diagnostic Pathology
Levertijd ongeveer 9 werkdagen
Gratis verzonden
Samenvatting
Covering all aspects of neuropathology, this updated volume in the Diagnostic Pathology series is an excellent point-of-care resource for pathologists at all levels of experience and training—both as a quick reference and as an efficient review to improve knowledge and skills. The third edition is an easy-to-use, one-stop reference for the most recent clinical, pathological, histological, and molecular knowledge in the field. It offers complete information on lesions of the brain, sellar region, and peripheral nerves, as well as benign cysts and selected infectious, inflammatory, reactive, vascular, and cortical dysplastic lesions, enabling you to arrive at the correct diagnosis and prepare actionable, useful reports.
Incorporates new WHO Classification of Tumors of the Central Nervous System, 5th Edition
Offers information on neoplasms of the brain, sellar region, and peripheral nerves, as well as benign cysts and selected infectious, inflammatory, reactive, and vascular lesions, aiding you in arriving at the correct diagnosis
Emphasizes surgical pathology but also provides significant content on nonneoplastic diseases that present with focal lesions, especially those that are potentially misinterpreted as neoplasms
Features new and updated chapters detailing several types of tumors that have been reclassified due to recent molecular driver information, cIMPACT-NOW recommendations, and the WHO Classification, 5th Edition
Features nearly 1,700 annotated images throughout, including neuroimaging studies, histology and immunohistochemical stains, and high-quality medical illustrations
Incorporates time-saving features such as a templated, highly formatted design; concise, bulleted text; a variety of test data tables; key facts in each chapter; and an extensive index Includes the enhanced eBook version, which allows you to access all text, figures, and references on a variety of devices
Specificaties
ISBN13:9780323713306
Taal:Engels
Bindwijze:Gebonden
Uitgever:Elsevier Health Sciences
Serie:Diagnostic Pathology
Inhoudsopgave
<p>Neoplastic</p> <U> <p>Brain and Spinal Cord</U></p> <p>Diffuse Astrocytic and Oligodendroglial Tumors</p> <p>Diffuse Astrocytoma, IDH-Mutant, WHO Grade II</p> <p>Diffuse Astrocytoma, IDH-Wildtype, WHO Grade II (Provisional Entity)</p> <p>Anaplastic Astrocytoma, IDH-Mutant, WHO Grade III</p> <p>Anaplastic Astrocytoma, IDH-Wildtype, WHO Grade III</p> <p>Glioblastoma, IDH-Wildtype</p> <p>Granular Cell Astrocytoma of the Cerebrum</p> <p>Gliosarcoma</p> <p>Glioblastoma, IDH Mutant</p> <p>Diffuse Midline Glioma, H3 K27M Mutant</p> <p>H3 G34-Mutant Gliomas, IDH-Wildtype (Provisional Entity)</p> <p>Oligodendroglioma</p> <p>Anaplastic Oligodendroglioma</p> <p>Mixed Oligoastrocytoma</p> <p>Other Astrocytic Tumors</p> <p>Pilocytic Astrocytoma</p> <p>Pilomyxoid Astrocytoma</p> <p>Subependymal Giant Cell Astrocytoma</p> <p>Pleomorphic Xanthoastrocytoma</p> <p>Anaplastic Pleomorphic Xanthoastrocytoma</p> <p>Pediatric Low-Grade Glioma/Glioneuronal Tumors (Provisional Entities)</p> <p>Ependymal Tumors</p> <p>Subependymoma</p> <p>Myxopapillary Ependymoma</p> <p>Ependymoma</p> <p>Ependymoma, *RELA* Fusion-Positive</p> <p>Anaplastic Ependymoma</p> <p>Other Gliomas</p> <p>Chordoid Glioma of 3rd Ventricle</p> <p>Angiocentric Glioma</p> <p>Astroblastoma</p> <p>Choroid Plexus Tumors</p> <p>Choroid Plexus Papilloma and Atypical Papilloma</p> <p>Choroid Plexus Carcinoma</p> <p>Neuronal and Mixed Neuronal-Glial Tumors </p> <p>Dysembryoplastic Neuroepithelial Tumor</p> <p>Gangliocytoma and Ganglioglioma</p> <p>Dysplastic Cerebellar Gangliocytoma (Lhermitte-Duclos Disease)</p> <p>Desmoplastic Infantile Ganglioglioma</p> <p>Papillary Glioneuronal Tumor</p> <p>Rosette-Forming Glioneuronal Tumor of 4th Ventricle</p> <p>Diffuse Leptomeningeal Glioneuronal Tumor</p> <p>Malignant Glioneuronal Tumors</p> <p>Central Neurocytoma</p> <p>Extraventricular Neurocytoma</p> <p>Cerebellar Liponeurocytoma</p> <p>Paraganglioma of Filum Terminale</p> <p>Tumors of the Pineal Region</p> <p>Pineal Parenchymal Neoplasms</p> <p>Papillary Tumor of the Pineal Region</p> <p>Pineal Anlage Tumor</p> <p>Embryonal Tumors</p> <p>Medulloblastoma</p> <p>CNS Embryonal Neoplasms</p> <p>Embryonal Tumor With Multilayered Rosettes, C19MC Altered</p> <p>Ewing Sarcoma</p> <p>Atypical Teratoid/Rhabdoid Tumor</p> <p>Germ Cell Tumors</p> <p>Germinoma</p> <p>Teratomas</p> <p>Other Germ Cell Tumors</p> <p>Lymphomas and Histiocytic Tumors</p> <p>Primary Central Nervous System Lymphoma</p> <p>Lymphomatosis Cerebri</p> <p>Lymphomatoid Granulomatosis</p> <p>Intravascular Lymphomatosis</p> <p>Primary Amyloidoma</p> <p>Langerhans Cell Histiocytosis</p> <p>Erdheim-Chester Disease</p> <p>Rosai-Dorfman Disease</p> <p>Metastatic Tumors</p> <p>Metastatic Neoplasms, Intraparenchymal, Brain and Spinal Cord</p><U> <p>Sellar Region</U></p> <p>Adenohypophyseal Neoplasia and Hyperplasia</p> <p>Pituitary Adenoma</p> <p>Prolactinoma</p> <p>Somatotroph Adenoma</p> <p>Corticotroph Adenoma</p> <p>Gonadotroph Adenoma</p> <p>Thyrotroph Adenoma</p> <p>Plurihormonal Adenoma</p> <p>Null Cell Adenoma</p> <p>Pituitary Hyperplasia</p> <p>Pituitary Carcinoma</p> <p>TTF-Mediated Neurohypophyseal Neoplasms</p> <p>Granular Cell Tumor of the Sellar Region</p> <p>Pituicytoma</p> <p>Spindle Cell Oncocytoma</p> <p>Craniopharyngiomas</p> <p>Adamantinomatous Craniopharyngioma</p> <p>Papillary Craniopharyngioma</p> <p>Miscellaneous Neoplasms </p> <p>Pituitary Blastoma</p> <p>Secondary Neoplasms of the Pituitary and Sellar Region</p> <p>Hypothalamic Hamartoma</p><U> <p>Meningiomas and Mesenchymal Nonmeningothelial Tumors</U></p> <p>Meningioma</p> <p>Solitary Fibrous Tumor/Hemangiopericytoma</p> <p>Hemangioblastoma</p> <p>Primary Melanocytic Neoplasms</p> <p>Osteocartilaginous Neoplasms</p> <p>Notochordal Tumors</p> <p>Fibrosarcoma</p> <p>Smooth Muscle Neoplasms</p> <p>Adipocytic Neoplasms</p> <p>Meningeal Glioma and Gliomatosis</p> <p>Metastatic Neoplasms, Intracranial and Intraspinal Meninges</p><U> <p>Tumors of Cranial and Paraspinal Nerves</U></p> <p>Schwannoma Variants</p> <p>Conventional Schwannoma</p> <p>Cellular Schwannoma</p> <p>Plexiform Schwannoma</p> <p>Melanotic Schwannoma</p> <p>Neurofibroma</p> <p>Plexiform Neurofibroma</p> <p>Localized Intraneural Neurofibroma</p> <p>Extraneural Neurofibroma Variants</p> <p>Perineurioma</p> <p>Intraneural Perineurioma</p> <p>Soft Tissue Perineurioma</p> <p>Primary Malignant Neoplasms of Nerve</p> <p>Malignant Peripheral Nerve Sheath Tumor</p> <p>Lipoma of 8th Cranial Nerve</p> <p>Lipoma of 8th Cranial Nerve</p><U> <p>Familial Tumor Syndromes</U></p> <p>Neurofibromatosis</p> <p>Neurofibromatosis 1</p> <p>Neurofibromatosis 2</p> <p>Schwannomatosis</p> <p>Other</p> <p>von Hippel-Lindau Syndrome</p> <p>Tuberous Sclerosis Complex</p> <p>Turcot Syndrome</p> <p>Nonneoplastic</p> <U> <p>Benign Cysts</U></p> <p>Arachnoid Cyst</p> <p>Epidermoid and Dermoid Cysts</p> <p>Colloid Cyst</p> <p>Rathke Cleft Cyst</p> <p>Endodermal Cyst</p> <p>Ependymal Cyst</p> <p>Pineal Cyst</p> <p>Facet Joint Synovial Cyst</p> <U> <p>Infectious, Inflammatory, and Reactive Lesions</U></p> <p>Demyelinating Diseases</p> <p>Demyelinating Disease (Multiple Sclerosis-Tumefactive Demyelination)</p> <p>Bacterial Infections</p> <p>Abscess and Cerebritis</p> <p>Whipple Disease</p> <p>Tuberculosis</p> <p>Viral Infections</p> <p>Herpes Simplex Encephalitis</p> <p>Progressive Multifocal Leukoencephalopathy</p> <p>HIV Encephalitis</p> <p>Other Viral Infections</p> <p>Fungal Infections</p> <p>Fungal Infections</p> <p>Protozoal and Parasitic Infections</p> <p>Toxoplasmosis</p> <p>Amebiasis</p> <p>Cysticercosis</p> <p>Miscellaneous Parasitic Infections</p> <p>Other Inflammatory Diseases</p> <p>Sarcoidosis</p> <p>Rasmussen Encephalitis</p> <p>Paraneoplastic Disease</p> <p>Textiloma (Muslinoma, Gauzoma, Gossypiboma)</p> <p>Inflammatory Pseudotumors</p> <p>Lymphocytic Hypophysitis</p> <p>Reactive Conditions and Noninflammatory Pseudoneoplasms</p> <p>Meningioangiomatosis</p> <p>Meningeal Response to Intracranial Hypotension</p> <p>Radiation Necrosis</p> <p>Calcifying Pseudoneoplasm of the Neuraxis</p> <U> <p>Vascular Diseases</U></p> <p>Vascular Malformations and Neoplasms</p> <p>Telangiectasis</p> <p>Cavernous Angioma</p> <p>Arteriovenous Malformation</p> <p>Capillary Hemangioma</p> <p>Vascular Lesions</p> <p>Subdural Hematoma</p> <p>Infarct</p> <p>Vasculitis and Vasculopathy</p> <p>Primary Angiitis of Central Nervous System</p> <p>Amyloid (Congophilic) Angiopathy</p> <U> <p>Cortical Dysplasia</U></p> <p>Cortical Dysplasia</p>