Your browser doesn't support javascript.
loading
Atypical teratoid/rhabdoid tumor of the sellar region in adult women: Is it a sex-related disease?
Nishikawa, Akihiro; Ogiwara, Toshihiro; Nagm, Alhusain; Sano, Kenji; Okada, Maki; Chiba, Akihiro; Agata, Masahiro; Kaneko, Tomoki; Tamada, Hisashi; Uehara, Takeshi; Hongo, Kazuhiro.
Afiliação
  • Nishikawa A; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ogiwara T; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan. Electronic address: togiwara@shinshu-u.ac.jp.
  • Nagm A; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan; Department of Neurosurgery, Al-Azhar University Faculty of Medicine-Nasr city, Cairo, Egypt.
  • Sano K; Department of Pathology, Iida Municipal Hospital, Iida, Japan.
  • Okada M; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
  • Chiba A; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
  • Agata M; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kaneko T; Department of Radiology, Shinshu University School of Medicine, Matsumoto, Japan.
  • Tamada H; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Uehara T; Department of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Hongo K; Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
J Clin Neurosci ; 49: 16-21, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29248378
ABSTRACT
Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant embryonal tumor in children and a rare entity. Although adult AT/RT is extremely rare, some cases of adult-onset AT/RT in the sellar region have been described. Here, we report an adult patient with AT/RT of the sellar region in whom it was difficult to make a definitive diagnosis and the clinical course was aggressive. This is the first report of autopsy findings that could confirm the clinical characteristics of this rare unresolved pathology, and will contribute to the improvement of prognosis. In addition, a literature review was performed to clarify this exceptionally rare condition. Interestingly, all reported adult patients with sellar AT/RT, along with the present case, were female. This raises the possibility of its being a sex-related disease. However, further studies are required to come to a definitive conclusion.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Sela Túrcica / Teratoma / Tumor Rabdoide Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Sela Túrcica / Teratoma / Tumor Rabdoide Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article