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1例起源于中颅窝的颅内恶性蝾螈瘤罕见病例:病例报告及文献复习

A rare case of intracranial malignant triton tumor arising in the middle cranial fossa: a case report and review of the literature.

作者信息

Bruzzone Eros, Melloni Ilaria, Barra Salvina, Fraternali Orcioni Giulio, Cocito Leonardo

出版信息

Folia Neuropathol. 2018;56(3):229-234. doi: 10.5114/fn.2018.78704.

Abstract

We describe a rare case of intracranial malignant triton tumor (MTT) arising in the middle cranial fossa in a 74-year-old female patient who had previously been exposed to radiation in the Chernobyl disaster. The patient underwent a surgical subtotal removal of the mass and radiation therapy, but the progression-free survival was only 2.5 months and death occurred four months after the onset of symptoms. MTTs are rare aggressive tumors arising from the nerve sheath showing rhabdomyosarcomatous differentiation and associated with a poor prognosis. The intracranial location is very rare, and only 10 cases, including the present report, have been described so far. Among intracranial MTTs, the cerebellopontine angle is the most common location. Neurofibromatosis type 1 (NF-1) and radiation exposure are risk factors as for MTTs located in other sites. The gold standard therapy is surgical excision followed by radiation therapy, but the prognosis is usually very poor.

摘要

我们描述了一例罕见的颅内恶性蝾螈瘤(MTT),发生于一名74岁女性患者的中颅窝,该患者曾在切尔诺贝利灾难中受到辐射。患者接受了肿瘤大部分切除术及放射治疗,但无进展生存期仅2.5个月,症状出现四个月后死亡。MTT是一种罕见的侵袭性肿瘤,起源于神经鞘,具有横纹肌肉瘤分化,预后较差。颅内发生极为罕见,迄今为止,包括本报告在内仅描述了10例。在颅内MTT中,小脑脑桥角是最常见的部位。1型神经纤维瘤病(NF-1)和辐射暴露是其他部位MTT的危险因素。金标准治疗是手术切除后进行放射治疗,但预后通常很差。

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