基本説明
日常診療でよく遭遇する病理病変を逸早く確実に診断できるように、という趣旨で企画されたハイ・イールド病理学シリーズの第５弾。
Full Description
Save time diagnosing neuropathology specimens with Neuropathology, part of the growing High-Yield Pathology Series. Dr. Anthony Yachnis and Dr. Marie Rivera-Zengotita help you review the key features of neuropathology specimens, recognize the classic look of each disease, and quickly confirm your diagnosis. A logical format, excellent color photographs, concise bulleted text, and authoritative content will help you accurately identify hundreds of discrete disease entities.Find information quickly and easily with a templated, easy-to-reference format and concise, bulleted text.Confirm your diagnoses with superb color photographs that demonstrate the classic appearance of each disease. Depend on authoritative information from leading experts in the field.Access the full text online, perform quick searches, and download all the images at www.expertconsult.com.
Contents
I. BASIC REACTIONS A. Cerebral EdemaB. Hydrocephalus C. Herniations II. DEVELOPMENTAL DISORDERSA. MalformationsNeural Tube Defects HoloprosencephalyPosterior Fossa: Chiari MalformationsCerebellar Vermis MalformationsLhermitte-Duclos DiseaseNeuronal Migration Defects B. Acquired Developmental Defects Germinal Matrix HemorrhagePeriventricular Leukomalacia Gray Matter Lesions PorencephalyIII. CEREBROVASCULAR DISORDERSA. Cerebral Ischemia and Hypertensive Changes Ischemic Cerebrovascular Disease Hypertensive Cerebrovascular Disease: Ischemic Changes Hypertensive Cerebrovascular Disease: Spontaneous Intracerebral Hemorrhage Hypertensive Cerebrovascular Disease: Posterior Reversible Encephalopathy Syndrome (PRES) B. Intracranial Aneurysms Saccular ("Berry") Aneurysms Fusiform Aneurysms Infective ("Mycotic") Aneurysms C. Vascular Malformations Arteriovenous Malformations (AVM) Cavernous Angiomas (CA)Capillary TelangiectasisVenous AngiomaD. Vasculitis Giant Cell ArteritisPolyarteritis Nodosa (PAN)Primary CNS AngiitisE. Inherited Cerebrovascular Diseases Cerebral Amyloid AngiopathyCerebral Autosomal Dominant Ateriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)Moyamoya SyndromeIV. TRAUMA A. Closed vs Open (Penetrating) Head Trauma Contusion/Laceration (Including Coup and Contra Coup Lesions)Diffuse Axonal Injury (Diffuse Traumatic Brain Injury)B. Traumatic Intracranial Hemorrhage Epidural HematomaSubdural HematomaV. BRAIN TUMORSA. Diffuse Gliomas-AstrocyticDiffuse Astrocytoma Anaplastic Astrocytoma Glioblastoma Glioblastoma VariantsB. Diffuse Gliomas-OligdendroglialOligodendroglioma Anaplastic Oligodendroglioma Mixed Glioma (Oligosatrocytoma, Anaplastic Oligoastrocytoma)Gliomatosis CerebriC. Other Astrocytic TumorsPleomorphic Xanthoastrocytoma (PXA) Pilocytic Astrocytoma Subependymal Giant Cell Astrocytoma D. Ependymomas and Subependymoma Ependymoma Anaplastic Ependymoma Myxopapillary Ependymoma SubependymomaE. Tumors with Ependymal-like Features Angiocentric GliomaChordoid GliomaAstroblastoma F. Choroid Plexus Tumors Choroid Plexus Papilloma Choroid Plexus CarcinomaG. Neuronal and Glioneuronal Tumors Ganglion Cell TumorsDesmoplastic Infantile Astrocytoma/Ganglioglioma Central NeurocytomaDysembryoplastic Neuroepithelial Tumor (DNET)Papillary Glioneuronal TumorRosette-Forming Glioneuronal Tumor of the Fourth VentricleH. Embryonal (Primitive) Neuroepithelial Tumors Medulloblastoma Central Nervous System - Primitive Neuroectodermal Tumor (CNS-PNET)Atypical Teratoid/Rhabdoid Tumors (AT/RT)I. Meningiomas (Tumors of the Meninges) Meningioma: Overview and General CharacteristicsMeningioma: WHO Grade I Variants Atypical Meningioma Malignant (Anaplastic) Meningiomas Hemangiopericytoma: Solitary Fibrous Tumor J. Nerve Sheath Tumors Schwannoma NeurofibromaPerineuriomaMalignant Peripheral Nerve Sheath Tumor (MPNST)K. Primary CNS Lymphoma (PCNSL) L. Pineal Parenchymal Tumors PineocytomaPineal Parenchymal Tumor of Intermediate Differentiation PineoblastomaPapillary Tumor of the Pineal Region M. Germ Cell Tumors of the Central Nervous System GerminomaOther Germ Cell Tumors N. Hemangioblastoma O. Sellar and Suprasellar Tumors Pituitary adenomasPituicytoma Cranopharyngioma Rathke cleft cystLangerhans cell histiocytosis P. Primary Melanocytic Tumors of the Central Nervous System Q. Central Nervous System Cysts R. Metastatic Brain Tumors S. Tumors of the Skull Base Chordoma of Skull BaseChondrosarcoma of Skull BaseVI. INFECTIOUS DISEASES A. Bacterial InfectionsAcute Purulent MeningitisCerebral Bacterial AbscessNocardia/Actinomycetes SpeciesMycobacterial InfectionNeurosyphilisB. MycosesCerebral Cryptococcosis AspergillosisMucormycosisCandidiasis C. Parasitic InfectionsCerebral ToxoplasmosisCerebral CystecercosisPrimary Amoebic MeningoencephalitisGranulomatous Amoebic EncephalitisCerebral MalariaD. Viral InfectionsGeneral viral effects on the nervous systemHerpes Simplex EncephalitisCytomegalovirus EncephalitisRabies encephalitisArbovirusesProgressive Multifocal LeukoencephalopathyE. Neuropathology of AIDSPrimary effects of HIV infectionHIV-Associated Vacuolar Myelopathy (HAM)Opportunistic CNS Infections in AIDSCNS Immune Reconstitution Inflammatory Syndrome (Neuro-IRIS)F. Prion DiseasesPrion-related diseases (Overview)Creutzfeldt-Jacob diseaseOther prion-related diseasesVII. Neurodegenerative disorders A. Alzheimer's DiseaseB. Frontotemporal Lobar Degenerations and Related TauopathiesCorticobasal Degeneration (Rebeiz Disease)Progressive Supranuclear Palsy (PSP: Steele-Richardson-Olszewski Syndrome)Pick DiseaseFrontotemporal Lobar Degeneration: Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 (FTDP-17)C. Frontotemporal Lobar Degenerations with Ubiquitin-Inclusions (FTLD-U/FTLD-MND (TDP-43)D. Parkinson's Disease and Related Alpha-SynucleinopathiesParkinson's DiseaseDementia with Lewy BodiesMultiple System Atrophy (MSA)E. Amyotrophic Lateral Sclerosis (ALS)F. Triple-Repeat Inherited NeurodegenerationsHuntington DiseaseAutosomal Recessive Spinocerebellar Degeneration (Friedrich's Ataxia)Autosomal Dominant Spinocerebellar Ataxias (SCA)Fragile X Tremor / Ataxia SyndromeG. Neuroaxonal DystrophiesNeurodegeneration with brain iron accumulation type 1 (NBIA 1)Other inherited neuroaxonal dystrophiesH. Vascular Dementia and Binswanger DiseaseVIII. DEMYELINATING DISEASES A. Multiple sclerosis Multiple SclerosisNeuromyelitis Optica Spectrum DisordersB. Acute Disseminated Leukoencephalitis C. Acute Hemorrhagic Leukoencephalitis (Hurst Disease)D. Tumefactive Demyelinating Lesions (TDL)IX. TOXIC, NUTRITIONAL, METABOLIC DISEASES A. Toxic InjuryToxic LeukoencephalopathyCarbon monoxideEthanol-related injury (including superior vermis atrophy and central pontine myelinolysis)Hepatic encephalopathyB. Nutritional DiseasesWernicke-Korsakoff diseaseSubacute Combined DegenerationC. Metabolic DiseasesNeuronal Storage DiseaseLeukodystrophiesNeuronal Ceroid LipofuscinosisWilson Disease (Hepatolenticular Degeneration)Alexander diseaseX. Neuromuscular disorders A. Peripheral Nerve DiseaseBasic reactions in peripheral nerve disordersImmune-Mediated Inflammatory NeuropathiesCharcot-Marie-Tooth disease and related congenital neuropathiesB. Skeletal Muscle DiseasesEssential Features: Myopathic versus Neurogenic ChangesDermatomyositisPolymyositisInclusion Body Myopathy and MyositisDystrophinopathies (Duchenne and Becker Muscular DystrophyMyotonic DystrophiesPeriodic ParalysisLimb-Girdle Muscular DystrophiesNemaline MyopathyCentral Core DiseasePompe DiseaseMcArdle DiseaseMitochondiral Myopathies
