Paediatrische Radiologie: Stützgewebe-Zentralnervensystem-Syndrome, Vol. I, by Franz Schmid. Berlin/Heidelberg/New York: Springer-Verlag, 1972, 504 pp., $78.70

PEDIATRICS ◽  
1973 ◽  
Vol 52 (4) ◽  
pp. 630-631
Author(s):  
Edward B. D. Neuhauser
Keyword(s):  
New York ◽  
Central Nervous System ◽  
Nervous System ◽  
Pediatric Radiology ◽  
Soft Tissues ◽  
Full Time ◽  
The Central Nervous System

Only the first volume of this projected two-volume textbook of pediatric radiology is available for review. Included in the first volume is a discussion of bones and soft tissues, the central nervous system, and 100 pages of syndromes in brief tabulated form. This is a handsome book written in German with 451 excellent illustrations. Few of the 16 contributing authors are well known in this country and it would seem that few are full-time pediatric radiologists.

Desmoplastic Medulloblastoma Metastatic to the Pancreas: Case Report

Neurosurgery ◽  
1991 ◽  
Vol 29 (4) ◽  
pp. 612-616 ◽  
Author(s):  
Hendrikus G.J. Krouwer ◽  
John Vollmerhausen ◽  
Joel White ◽  
Michael D. Prados
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Soft Tissues ◽  
Extraneural Metastases ◽  
Organ Systems ◽  
Multidrug Chemotherapy ◽  
The Central Nervous System ◽  
Desmoplastic Medulloblastoma ◽  
Local Radiation ◽  
Weiss Criteria

Abstract A case is reported in which a desmoplastic medulloblastoma metastasized to the pancreas and to the surrounding soft tissues but did not recur locally or disseminate within the central nervous system. Multidrug chemotherapy and local radiation therapy resulted in a complete remission. In all four previously reported cases of medulloblastoma metastasizing to the pancreas, the diagnosis was not made until the postmortem examination, and all of these patients also had extensive metastases in other organ systems. Modification of the Weiss criteria defining extraneural metastases from tumors of the central nervous system is suggested.

Clinical Electroencephalography of Children Vol. II, edited by Peter Kellaway and Ingemar Peterśen. New York/London: Grune & Stratton, Inc., 1968, 332 pp., $16.75

PEDIATRICS ◽  
1969 ◽  
Vol 44 (5) ◽  
pp. 785-786
Author(s):  
Cesare T. Lombroso
Keyword(s):  
New York ◽  
Central Nervous System ◽  
Nervous System ◽  
Early Life ◽  
Normal Development ◽  
Clinical Neurophysiology ◽  
The Central Nervous System ◽  
The Subject

This book contains twenty papers read in the summer of 1967 at a conference in Gäteborg, Sweden. This was the second symposium within the span of 4 years on the subject of electroencephalognaphy and clinical neurophysiology relating to early life. The holding of the conference is certainly an index of the great surge of interest among pediatricians, neurologists and neurophysiologists in matters pertaining to the normal development of the central nervous system as well as in the pathologic deviations of this system.

Ewing's Family of Tumors Involving Structures Related to the Central Nervous System: A Review

2000 ◽  
Vol 3 (3) ◽  
pp. 203-210 ◽  
Author(s):  
M. Gary Hadfield ◽  
Martha M. Quezado ◽  
Robert L. Williams ◽  
Vivian Y. Luo
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Soft Tissues ◽  
Case Reports ◽  
Spinal Column ◽  
Diagnostic Methods ◽  
Electron Microscopic ◽  
Adjacent Structures ◽  
Microscopic Features ◽  
The Central Nervous System

This review consolidates information gleaned from several case reports and larger series on Ewing's sarcoma family of tumors (EFT) involving structures related to and found in the central nervous system (CNS). These tumors involve the skull, the spinal column, adjacent soft tissues, the meninges, and the brain. We have separated the cases by skull region and spinal column level, and we discuss the attendant differences in prognosis following treatment by neurosurgery, radiation, and chemotherapy. Light and electron microscopic features can be used to differentiate EFT from other small round blue cell tumors that involve the CNS (central primitive neuroectodermal tumor, lymphoma, etc.). Recent molecular and genetic findings in EFT provide new diagnostic methods. We conclude that EFT involving the CNS and adjacent structures is not so rare as previously stated and that the prognosis is more favorable, as a rule, than for the more common examples arising in the long bones and pelvis.

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