By William W. Campbell
This seventh version of Dejong’s The Neurological exam deals practitioners and citizens of Neurology an in-depth dialogue of neurologic tests that may not be came across anyplace else.
Without leaving behind vintage thoughts and technological know-how, this definitive resource on neurologic exam strategies has been streamlined and up-to-date. The textual content integrates info of neuroanatomy and medical prognosis in an easy-to-read structure. Anatomical and examination illustrations aid verify right strategy. Plus, illustrative circumstances and tables summarize differentials and checklist scientific findings. With this booklet as their consultant, readers will really comprehend the anatomical underpinnings of exam techniques.
• Four-color design
• up-to-date figures and references
• textual content is supplemented via invaluable containers that spotlight key points
• while on hand, evidence-based scientific insights are integrated in assessing the price of particular tests
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Additional info for DeJong's The Neurologic Examination (7th Edition)
It has a characteristic broad, nodular growth pattern. As with neuroblastic tumors at other sites, the neoplastic cells have a neural immunophenotype and ultrastructure. Homer Wright–type rosettes (with central neuroﬁbrillary processes) or, occasionally, Flexner-Wintersteiner rosettes (with central lumina) may be seen. A high mitotic rate and necrosis tend to indicate aggressive biologic behavior. Pineal Parenchymal Tumors The pineal gland is made up of cells having phenotypic characteristics of retinal photoreceptors, with which they share a common embryonic lineage.
Favorable clinical outcome is also highly correlated with age less than 1 year, conﬁnement of tumor to the adrenal gland, and histologic parameters such as a low mitosis-karyorrhexis index. Better-differentiated tumors consisting of neuroblasts, differentiating neuroblasts, and mature ganglion cells with more abundant schwannian stroma are known as ganglioneuroblastomas, and tumors consisting entirely of schwannian stroma with scattered mature ganglion cells are designated ganglioneuromas. Olfactory Neuroblastoma.
Age and sex distribution, location, clinical presentation, and imaging features are all similar to those of WHO grade II oligodendroglioma. Two histologic variants have been recognized: a “compact” or biphasic variant and a “diffuse” or intermingled variant. Neither the astrocytic nor the oligodendroglial component should have anaplastic histology. The diagnosis of oligoastrocytoma is usually easier and less controversial in the biphasic variant, which shows distinct areas of oligodendroglial and astrocytic differentiation.
DeJong's The Neurologic Examination (7th Edition) by William W. Campbell