Journal of neurosurgery. Pediatrics · 2016
Phosphaturic mesenchymal tumor of the brain without tumor-induced osteomalacia in an 8-year-old girl: case report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Ellis Mark B, Gridley Daniel, Lal Suresh, Nair Geetha R, Feiz-Erfan Iman
Аннотация
Phosphaturic mesenchymal tumor (mixed connective tissue variant) (PMT-MCT) are tumors that may cause tumor-induced osteomalacia and rarely appear intracranially. The authors describe the case of an 8-year-old girl who was found to have PMT-MCT with involvement of the cerebellar hemisphere and a small tumor pedicle breaching the dura mater and involving the skull. This was removed surgically in gross-total fashion without further complication. Histologically the tumor was confirmed to be a PMT-MCT. There was no evidence of tumor-induced osteomalacia. At the 42-month follow-up, the patient is doing well, has no abnormalities, and is free of recurrence. PMT-MCTs are rare tumors that may involve the brain parenchyma. A gross-total resection may be effective to cure these lesions.
Предметные рубрики MeSH
AtaxiaBiomarkers, TumorCerebellar NeoplasmsChildDiagnosis, DifferentialFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsGene Expression Regulation, NeoplasticHumansHypophosphatemiaHypophosphatemia, FamilialMagnetic Resonance ImagingMesenchymomaOsteomalaciaReverse Transcriptase Polymerase Chain ReactionSkull NeoplasmsTomography, X-Ray ComputedTreatment Outcome