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Synchronous glioblastoma and medulloblastoma in a child with mismatch repair mutation.

Authors :
Amayiri, Nisreen
Al-Hussaini, Maysa
Swaidan, Maisa
Jaradat, Imad
Qandeel, Monther
Tabori, Uri
Hawkins, Cynthia
Musharbash, Awni
Alsaad, Khulood
Bouffet, Eric
Source :
Child's Nervous System. Mar2016, Vol. 32 Issue 3, p553-557. 5p.
Publication Year :
2016

Abstract

Synchronous primary malignant brain tumors are rare. We present a 5-year-old boy with synchronous glioblastoma and medulloblastoma. Both tumor samples had positive p53 stain and loss of PMS2 and MLH1 stains. The child had multiple café au lait spots and a significant family history of cancer. After subtotal resection of both tumors, he received craniospinal radiation with concomitant temozolomide followed by chemotherapy, alternating cycles of cisplatin/lomustine/vincristine with temozolomide. Then, he started maintenance treatment with cis-retinoic acid (100 mg/m/day for 21 days). He remained asymptomatic for 34 months despite a follow-up brain MRI consistent with glioblastoma relapse 9 months before his death. Cis-retinoic acid may have contributed to prolong survival in this child with a probable biallelic mismatch repair syndrome. [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
*DNA repair
*TRETINOIN

Details

Language :
English
ISSN :
02567040
Volume :
32
Issue :
3
Database :
Academic Search Index
Journal :
Child's Nervous System
Publication Type :
Academic Journal
Accession number :
113445109
Full Text :
https://doi.org/10.1007/s00381-015-2883-3