Abstract

We present a case of myelodysplastic syndrome (MDS) following treatment for medulloblastoma. The tumor was diagnosed at 15 years of age and managed with surgery, craniospinal radiation and a triple-durg regimen [chloroethylnitrosourea (CCNU), vincristine (VCR), procarbazine]. Fifteen months after the completion of therapy, the patient developed MDS with monosomy 5 and monosomy 7 on chromosome analysis of bone marrow cells. Two weeks later, MDS evolved into acute myeloblastic leukemia (AML). Therapy-related MDS or AML may be a complication for patients with past brain tumors. Therefore, they should be carefully followed up by regular physical examinations and complete blood counts.

Keywords: medulloblastoma, myelodysplastic syndrome, second malignancy, monosomy 5, monosomy 7

How to cite

1.
Akyüz C, Emir S, Güler N, Türker A, Büyükpamukçu M. Myelodysplastic syndrome in a child with a history of medulloblastoma. Turk J Pediatr 1998; 40: 131-134. https://doi.org/10.24953/turkjpediatr.1998.3291