Atypical Presentation of Atypical Teratoid Rhabdoid Tumor in a Child

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Atypical Presentation of Atypical Teratoid Rhabdoid Tumor in a Child

Atypical Teratoid Rhabdoid Tumor (ATRT) is a rare malignant intracranial neoplasm more commonly diagnosed in young children. The authors report the case of an 11-year-old boy with a long standing history of slowly progressive weight loss, fatigue, and weakness over 1.5 years whose magnetic resonance imaging revealed a large heterogeneous enhancing dorsally exophytic lower brainstem mass. Examin...

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Atypical teratoid rhabdoid tumor in adulthood.

Sir, – Atypical teratoid rhabdoid tumor (AT/RT) is a rare tumor that predominates in infancy. It is an aggressive tumor with dismal outcome. We report a case of AT/ RT in a 44-year-old female who presented with headache. The tumor was localized in the right occipital lobe. Gross total resection, chemotherapy, and radiotherapy were administered, and the patient is alive 9 months since diagnosis ...

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Atypical teratoid/rhabdoid tumor mimicking tuberculous meningitis.

Atypical teratoid/rhabdoid tumor of the central nervous system is a highly malignant neoplasm in infants and young children. We report a 6 year-old girl with atypical teratoid/rhabdoid tumor. Based on cerebrospinal fluid examination MRI scan and family history of tuberculosis; we diagnosed tuberculous meningitis. There was inadequate response to the antituberculosis therapy; so we performed ste...

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CASE REPORT Atypical Teratoid/Rhabdoid Tumor of the Spine

K.K. Moeller S. Coventry S. Jernigan T.M. Moriarty SUMMARY: Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant central nervous system neoplasm usually seen in young children and infants. Prognosis for AT/RT is poor, with most patients dying within 1 year of presentation. AT/RT most commonly occurs intracranially. Location in the spine, though previously reported, is rare, and imagin...

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Primary atypical teratoid rhabdoid tumor in the adult spine

BACKGROUND Atypical teratoid/rhabdoid tumor (ATRT) is a highly aggressive tumor of the central nervous system (WHO grade IV), which is most frequently found intracranially in young children and infants. Only three prior cases of primary ATRT involving the adult spine were found following a literature review, and the average survival for these patients was only 20 postoperative months. CASE DE...

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ژورنال

عنوان ژورنال: Case Reports in Oncological Medicine

سال: 2013

ISSN: 2090-6706,2090-6714

DOI: 10.1155/2013/815923