Erschienen in:
21.07.2016 | Case Report
Ultra early recurrence in giant congenital malignant rhabdoid tumor of spine
verfasst von:
Navneet Singla, Ankur Kapoor, Debajyoti Chatterjee, B. D. Radotra
Erschienen in:
Child's Nervous System
|
Ausgabe 12/2016
Einloggen, um Zugang zu erhalten
Abstract
Background
Malignant rhabdoid tumor (MRT) is an aggressive tumor of infancy and childhood that rarely presents as a primary spinal or spinal cord tumor. There are only three reported cases of spinal MRT in infants.
Objective
We present a similar case in a 3-month male child who developed ultra-early recurrence, 4 weeks after complete excision. The diagnosis was confirmed by immunohistochemistry showing inactivation of the INI1 gene.
Result
Despite surgical excision and adjuvant chemoradiotherapy, these tumors have a progressive course and recurrence is a common phenomenon.
Conclusion
We believe that MRT must be considered in the differential diagnosis of the intra/paraspinal masses, especially in the infants.