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Diagn Pathol ; 10: 47, 2015 May 02.
Article in English | MEDLINE | ID: mdl-25934090

ABSTRACT

Atypical teratoid/rhabdoid tumors are rare and highly malignant central nervous system tumors. They have no specific radiological features and often present several histological components that make a problem in differential diagnosis with medulloblastoma and primitive neuroectodermal tumors. We present the case of a newborn girl complained of a gradual proptosis of the left eye secondary to an expansive lesional process of the optic nerve. The location at the optic nerve, reported only twice in the literature, and an exclusive rhabdoid appearance on biopsy added additional differential diagnosis problems. The proptosis worsened and the infant died few days after two cycles of chemotherapy. VIRTUAL SLIDES: The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/2037718783145212 .


Subject(s)
Optic Nerve Neoplasms/pathology , Rhabdoid Tumor/pathology , Teratoma/pathology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biomarkers, Tumor/analysis , Biopsy , Diagnosis, Differential , Fatal Outcome , Female , Humans , Immunohistochemistry , Infant, Newborn , Magnetic Resonance Imaging , Optic Nerve Neoplasms/chemistry , Optic Nerve Neoplasms/drug therapy , Predictive Value of Tests , Rhabdoid Tumor/chemistry , Rhabdoid Tumor/drug therapy , Teratoma/chemistry , Teratoma/drug therapy , Treatment Failure
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