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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.
Table of Contents:
Neural Tube Defects
Holoprosencephaly
Posterior Fossa: Chiari Malformations
Cerebellar Vermis Malformations
Lhermitte-Duclos Disease
Neuronal Migration Defects
Germinal Matrix Hemorrhage
Periventricular Leukomalacia
Gray Matter Lesions
Porencephaly
Ischemic Cerebrovascular Disease
Hypertensive Cerebrovascular Disease: Ischemic Changes
Hypertensive Cerebrovascular Disease: Spontaneous Intracerebral Hemorrhage
Hypertensive Cerebrovascular Disease: Posterior Reversible Encephalopathy Syndrome (PRES)
Saccular ("Berry") Aneurysms
Fusiform Aneurysms
Infective ("Mycotic") Aneurysms
Arteriovenous Malformations (AVM)
Cavernous Angiomas (CA)
Capillary Telangiectasis
Venous Angioma
Giant Cell Arteritis
Polyarteritis Nodosa (PAN)
Primary CNS Angiitis
Cerebral Amyloid Angiopathy
Cerebral Autosomal Dominant Ateriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Moyamoya Syndrome
Contusion/Laceration (Including Coup and Contra Coup Lesions)
Diffuse Axonal Injury (Diffuse Traumatic Brain Injury)
Epidural Hematoma
Subdural Hematoma
Diffuse Astrocytoma
Anaplastic Astrocytoma
Glioblastoma
Glioblastoma Variants
Oligodendroglioma
Anaplastic Oligodendroglioma
Mixed Glioma (Oligosatrocytoma, Anaplastic Oligoastrocytoma)
Gliomatosis Cerebri
Pleomorphic Xanthoastrocytoma (PXA)
Pilocytic Astrocytoma
Subependymal Giant Cell Astrocytoma
Ependymoma
Anaplastic Ependymoma
Myxopapillary Ependymoma
Subependymoma
Angiocentric Glioma
Chordoid Glioma
Astroblastoma
Choroid Plexus Papilloma
Choroid Plexus Carcinoma
Ganglion Cell Tumors
Desmoplastic Infantile Astrocytoma/Ganglioglioma
Central Neurocytoma
Dysembryoplastic Neuroepithelial Tumor (DNET)
Papillary Glioneuronal Tumor
Rosette-Forming Glioneuronal Tumor of the Fourth Ventricle
Medulloblastoma
Central Nervous System - Primitive Neuroectodermal Tumor (CNS-PNET)
Atypical Teratoid/Rhabdoid Tumors (AT/RT)
Meningioma: Overview and General Characteristics
Meningioma: WHO Grade I Variants
Atypical Meningioma
Malignant (Anaplastic) Meningiomas
Hemangiopericytoma: Solitary Fibrous Tumor
Schwannoma
Neurofibroma
Perineurioma
Malignant Peripheral Nerve Sheath Tumor (MPNST)
Pineocytoma
Pineal Parenchymal Tumor of Intermediate Differentiation
Pineoblastoma
Papillary Tumor of the Pineal Region
Germinoma
Other Germ Cell Tumors
Pituitary adenomas
Pituicytoma
Cranopharyngioma
Rathke cleft cyst
Langerhans cell histiocytosis
Chordoma of Skull Base
Chondrosarcoma of Skull Base
Acute Purulent Meningitis
Cerebral Bacterial Abscess
Nocardia/Actinomycetes Species
Mycobacterial Infection
Neurosyphilis
Cerebral Cryptococcosis
Aspergillosis
Mucormycosis
Candidiasis
Cerebral Toxoplasmosis
Cerebral Cystecercosis
Primary Amoebic Meningoencephalitis
Granulomatous Amoebic Encephalitis
Cerebral Malaria
General viral effects on the nervous system
Herpes Simplex Encephalitis
Cytomegalovirus Encephalitis
Rabies encephalitis
Arboviruses
Progressive Multifocal Leukoencephalopathy
Primary effects of HIV infection
HIV-Associated Vacuolar Myelopathy (HAM)
Opportunistic CNS Infections in AIDS
CNS Immune Reconstitution Inflammatory Syndrome (Neuro-IRIS)
Prion-related diseases (Overview)
Creutzfeldt-Jacob disease
Other prion-related diseases
Corticobasal Degeneration (Rebeiz Disease)
Progressive Supranuclear Palsy (PSP: Steele-Richardson-Olszewski Syndrome)
Pick Disease
Frontotemporal Lobar Degeneration: Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 (FTDP-17)
Parkinson’s Disease
Dementia with Lewy Bodies
Multiple System Atrophy (MSA)
Huntington Disease
Autosomal Recessive Spinocerebellar Degeneration (Friedrich’s Ataxia)
Autosomal Dominant Spinocerebellar Ataxias (SCA)
Fragile X Tremor / Ataxia Syndrome
Neurodegeneration with brain iron accumulation type 1 (NBIA 1)
Other inherited neuroaxonal dystrophies
Multiple Sclerosis
Neuromyelitis Optica Spectrum Disorders
A. Toxic Injury
Toxic Leukoencephalopathy
Carbon monoxide
Ethanol-related injury (including superior vermis atrophy and central pontine myelinolysis)
Hepatic encephalopathy
B. Nutritional Diseases
Wernicke-Korsakoff disease
Subacute Combined Degeneration
C. Metabolic Diseases
Neuronal Storage Disease
Leukodystrophies
Neuronal Ceroid Lipofuscinosis
Wilson Disease (Hepatolenticular Degeneration)
Alexander disease
Basic reactions in peripheral nerve disorders
Immune-Mediated Inflammatory Neuropathies
Charcot-Marie-Tooth disease and related congenital neuropathies
Essential Features: Myopathic versus Neurogenic Changes
Dermatomyositis
Polymyositis
Inclusion Body Myopathy and Myositis
Dystrophinopathies (Duchenne and Becker Muscular Dystrophy
Myotonic Dystrophies
Periodic Paralysis
Limb-Girdle Muscular Dystrophies
Nemaline Myopathy
Central Core Disease
Pompe Disease
McArdle Disease
Mitochondiral Myopathies
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