| Literature DB >> 25112406 |
Wei Wang1, Xiao-Dong Chen, Hong-Min Bai, Qiu-Lin Liao, Xue-Jun Dai, Da-Yun Peng, Hui-Xia Cao.
Abstract
A 29-year-old male patient was admitted into hospital with the main complaint of progressive visual disturbance. Both CT SCAN and MRI demonstrated a cystic-solid contrast-enhancing sellar-suprasellar mass with obvious calcification. Histopathological examination of the first resected specimen showed a typical appearance of adamantinomatous craniopharyngioma. The patient received gamma knife therapy after his first operation because of partial tumor removal. He experienced two relapses in the subsequent 2 years, for which only surgical resection was performed. The later histopathology presented malignant appearance with tumor cells moderate to severe pleomorphism, hyperchromasia, increased nuclear cytoplastic ratio, high mitotic activity (30/10 high power fields) and focal coagulative necrosis. The patient died 9 months after identification of histologic malignancy. Clinical and histopathological features, biological behavior of one case of malignant craniopharyngioma were discussed, with a brief review of the relevant literature.Entities:
Keywords: craniopharyngioma; follow-up; malignant transformation; prognosis; radiotherapy
Mesh:
Year: 2014 PMID: 25112406 DOI: 10.1111/neup.12142
Source DB: PubMed Journal: Neuropathology ISSN: 0919-6544 Impact factor: 1.906