Radiation-induced tumors of the central nervous system occurring in childhood and adolescence - Four unusual lesions in three patients and a review of the literature
A. Amirjamshidi et K. Abbassioun, Radiation-induced tumors of the central nervous system occurring in childhood and adolescence - Four unusual lesions in three patients and a review of the literature, CHILD NERV, 16(7), 2000, pp. 390-397
The authors report four very rare radiation-associated tumors (or radiation
-induced tumors; RITs) of the central nervous system (CNS) and review the l
iterature on this topic. The purpose of this study was to determine the pos
sible relationship between the harmful effects of radiation therapy, the sh
ortest and the longest interval between the time of irradiation and the occ
urrence of the secondary tumor, and possible predisposing factors. The tumo
rigenic effects of therapeutic irradiation of the CNS have been mentioned i
n the literature, but the authors' literature search did not disclose eithe
r many reports of cases such as their own or a satisfactory and concise dis
cussion on the different aspects of the late and catastrophic complications
of this method of adjunct therapy to the CNS. Four rare cases of RIT in th
ree patients are presented: a unique case of intradural meningioma of the c
ervical spine, which was irradiated successfully only for the patient to pr
esent with a new high-grade cerebral astrocytoma 4 years later, a paraventr
icular cavernoma and a fronto-temporo-orbital chondrosarcoma. These second
RITs became symptomatic in the 17th, 16th and 15th years of life, respectiv
ely, in these young patients. The primary lesions were ependymomas, two in
the IV ventricle and one in the left hemisphere. The time intervals between
radiation and secondary tumor presentation were 14 and 18 years, 9 years a
nd 28 months, in the order in which these patients presented. All the patie
nts survived the second operation except the one with chondrosarcoma, who d
ied in spite of repeated surgical interventions and adjunct therapies. It i
s concluded that the development of secondary RITs does not necessarily req
uire a very long time interval; that although sarcomas ale the most common
RITs of the CNS in childhood and adolescence, benign and other rare and cur
able lesions may also occur in the field or vicinity of the field of radiat
ion; and that in view of the possibility of occurrence of different types o
f RITs after varying time intervals in a single patient, whole-life follow-
up of similar patients is mandatory.