Nishikawa Akihiro, Ogiwara Toshihiro, Nagm Alhusain, Sano Kenji, Okada Maki, Chiba Akihiro, Agata Masahiro, Kaneko Tomoki, Tamada Hisashi, Uehara Takeshi, Hongo Kazuhiro
Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.
J Clin Neurosci. 2018 Mar;49:16-21. doi: 10.1016/j.jocn.2017.12.010. Epub 2017 Dec 14.
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.
非典型畸胎样/横纹肌样瘤(AT/RT)是儿童中一种高度恶性的胚胎性肿瘤,较为罕见。虽然成人AT/RT极为罕见,但已有一些鞍区成人发病的AT/RT病例报道。在此,我们报告一例鞍区AT/RT的成年患者,该病例难以做出明确诊断,临床病程进展迅速。这是首例能证实这种罕见未解决病理临床特征的尸检报告,将有助于改善预后。此外,进行了文献综述以阐明这种极其罕见的病症。有趣的是,所有报道的鞍区AT/RT成年患者以及本病例均为女性。这增加了其为性别相关疾病的可能性。然而,需要进一步研究才能得出明确结论。