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J Adolesc Young Adult Oncol ; 8(6): 697-701, 2019 12.
Article in English | MEDLINE | ID: mdl-31314635

ABSTRACT

Primitive neuroectodermal tumor (PNET) is a rare and highly malignant neoplasm composed of small round cells, which frequently occurs in children and adolescents. PNET originating from the prostate is even rarer. We report a case of PNET of the prostate with notalgia and paraplegia as the initial symptoms. Positron emission tomography-computed tomography scanning showed hypodense and hypermetabolism on the prostate; subsequently, we ascertained the diagnosis by transrectal ultrasound-guided biopsy. The patient underwent local vertebral radiotherapy combined with five courses of systematic chemotherapy. Disease progressed after 11 months, and the overall survival was 17 months.


Subject(s)
Neoplasm Recurrence, Local/pathology , Neuroectodermal Tumors, Primitive/pathology , Paraplegia/pathology , Paresthesia/pathology , Prostatic Neoplasms/pathology , Pruritus/pathology , Adult , Combined Modality Therapy , Humans , Male , Neoplasm Recurrence, Local/therapy , Neuroectodermal Tumors, Primitive/therapy , Prognosis , Prostatic Neoplasms/therapy
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