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SKULL AND PARASPINAL NEOPLASMS, NONNEOPLASTIC MASSES, AND MALFORMATIONS

from 3 - Brain Tumors

Published online by Cambridge University Press:  04 August 2010

Hannes Vogel
Affiliation:
Stanford University School of Medicine, California
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Summary

A surprising number of cases come to the attention of the surgical neuropathologist that represent extraneural masses originating in the bone or other soft tissues, simply because these are within the spectrum of practice in neurosurgery. These represent a wide gamut of etiologies including primary and metastatic neoplasms, infections, malformations, and others. Just as in the proper evaluation of any CNS lesion, knowledge of the radiographic features and overall clinical circumstances is of paramount importance in making a correct diagnosis. Many of the entities listed below may be seen in association with either the skull or spinal column even though they all have distinct sites of predilection.

Among the following, the most common benign entities to involve the skull are fibrous dysplasia, Langerhans cell histiocytosis, osteoma, dermoid cysts, and hemangiomas.

Neoplasms of the skull and skull base may be best conceptualized as arising in one of the following compartments:

  • Pituitary region (Chapter 3G)

  • Nasal and paranasal sinus region, including olfactory neuroblastoma, olfactory neuroepithelioma, neuroendocrine carcinoma, nasopharyngeal carcinoma, juvenile angiofibroma, and mucocele

  • Orbital region, including meningioma, lymphoma, rhabdomyosarcoma, and malignant melanoma

  • Middle ear compartment, including paraganglioma, cholesteatoma, squamous cell carcinoma, and endolymphatic sac tumor

  • Skull base tumors, including chondroma, chondrosarcoma, chordoma, meningioma, and schwannoma

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Information
Nervous System , pp. 318 - 337
Publisher: Cambridge University Press
Print publication year: 2009

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