Atypical teratoid/rhabdoid tumor of the sellar region in adult women: Is it a sex-related disease?

被引:15
|
作者
Nishikawa, Akihiro [1 ]
Ogiwara, Toshihiro [1 ]
Nagm, Alhusain [1 ,2 ]
Sano, Kenji [3 ]
Okada, Maki [1 ]
Chiba, Akihiro [1 ]
Agata, Masahiro [1 ]
Kaneko, Tomoki [4 ]
Tamada, Hisashi [5 ]
Uehara, Takeshi [5 ]
Hongo, Kazuhiro [1 ]
机构
[1] Shinshu Univ, Dept Neurosurg, Sch Med, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[2] Al Azhar Univ, Dept Neurosurg, Fac Med, Cairo, Egypt
[3] Iida Municipal Hosp, Dept Pathol, Iida, Japan
[4] Shinshu Univ, Dept Radiol, Sch Med, Matsumoto, Nagano, Japan
[5] Shinshu Univ, Dept Lab Med, Sch Med, Matsumoto, Nagano, Japan
关键词
Malignant pituitary tumor; Atypical teratoid/rhabdoid tumor; Endoscopic transsphenoidal surgery; Treatment strategy; Sex-related disease; TERATOID RHABDOID TUMOR; CHILDHOOD; TURCICA; INFANCY;
D O I
10.1016/j.jocn.2017.12.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 21
页数:6
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