| Literature DB >> 11263505 |
E Gömöri1, D J Halbauer, T Dóczi, E Balázs, P Kajtár, L Pajor.
Abstract
We present a case of a germinoma in the sellar region of a 10-year-old female patient who presented with a history of polydipsia, polyuria and visual disturbances. The tumor was resected and histologically analyzed. Interphase cytogenetics was performed using chromosome specific (peri)-centromeric DNA probes for all the somatic and X chromosomes on fresh frozen tissues. Fluorescent in situ cell hybridization demonstrated accumulated cytogenetic abnormalities involving significant alterations of chromosome 1, 4, 5/19 and 15. The child was treated postoperatively by radiation and now appears well with only minor neurological deficits. At 3-year follow-up no recurrent tumor mass could be demonstrated.Entities:
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Year: 2000 PMID: 11263505 DOI: 10.1023/a:1006409217130
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130