Walsh & Hoyt: Congenital Neoplasms

Update Item Information
Identifier wh_ch32_p1547_1
Title Walsh & Hoyt: Congenital Neoplasms
Creator Karl C. Golnik, MD
Affiliation Departments of Ophthalmology, Neurology & Neurosurgery, University of Cincinnati & The Cincinnati Eye Institute
Subject Neoplasms; Congenital Neoplasms; Choristomas; Hamartomas; Congenital
Description Lesions in this category are considered to be neoplasms because of their growth rate and, in some cases, their malignant potential. Congenital neoplasms include germ cell tumors, lipomas, and craniopharyngiomas. Certain neuroectodermal neoplasms are occasionally observed in patients at or shortly after birth (e.g., primitive neuroectodermal tumors). Although these tumors arise from primitive cells that have not, in many cases, followed a normal path to maturation, they are not considered as examples of dysembryogenesis in the sense that the term is used in this chapter.
Date 2005
Language eng
Format application/pdf
Type Text
Source Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition
Relation is Part of Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology
Collection Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6nw2sq2
Setname ehsl_novel_whts
ID 185994
Reference URL https://collections.lib.utah.edu/ark:/87278/s6nw2sq2
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