Background: Atypical teratoid/rhabdoid tumor in adults is a relatively rare malignant
neoplasm. It is characterized by the presence of rhabdoid cells in combination with loss of …

Introduction Atypical teratoid/rhabdoid tumor (AT/RT) is a highly aggressive embryonal CNS
neoplasm, characterized by inactivation of SMARCB1 (INI1) or rarely of SMARCA4 (BRG1) …

Purpose: To assess the main imaging and clinical features in adult-and pediatric-onset
atypical teratoid rhabdoid tumor (ATRT) in order to build a predefined pathway useful for the …

Loss of function in SMARCB1/INI1 has been observed in a group of malignancies
collectively defined as SMARCB1/INI1-deficient neoplasms. Primary intracranial …

So-called primary yolk sac tumors of the vulva are very rare and often have an aggressive
disease course. Their molecular features have not been previously characterized. There is …

Abstract Introduction: Atypical Teratoid/Rhabdoid tumors are rare, highly malignant tumors in
adults, with a median survival of 20 months. We report a case of a sellar atypical …

Background: Adult sellar region atypical teratoid/rhabdoid tumor (AT/RT) is a rare lesion. We
aimed to elucidate clinical, radiologic, and pathological characteristics, treatment strategies …

Atypical teratoid rhabdoid tumor is a rare lesion that occurs mainly in children can be
supratentorial or infratentorial and it accounts for 1-2% of pediatric brain tumors and over …

Background Atypical teratoid/rhabdoid tumor (AT/RT) is well documented in children but less
so in adults because of its rarity. Method We report a series of five cases, a literature review …

Background Atypical teratoid/rhabdoid tumors (ATRT) are uncommon malignancies of the
central nervous system and are often difficult to distinguish radiographically and …