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Schwannoma in Sellar Region Mimics Invasive Pituitary Macroadenoma

机译:Sellar地区的神经鞘瘤模仿侵袭性垂体大腺瘤。

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摘要

In central nervous system, schwannomas, as ubiquitous tumors, mostly originate from sensory nerves like auditory and trigeminal nerves. However, intrasellar schwannomas are extremely rare. They are often misdiagnosed as pituitary adenomas.We report a rare case of schwannoma in the sellar region—a challenging diagnosis guided by clinical presentations, radiological signs, and postoperative pathological test.We represent a 65-year-old woman who had suffered from headaches, hypothyroidism, and visual disturbance. Her MRI revealed an abnormal sellar region mixed-signal mass lesion with suprasellar, left parasellar, and sellar floor invasiveness. We present detailed analysis of the patient's disease course and review relevant literatures. Written informed consent was obtained from the patient for publication of this article. A copy of the written consent is available for review by the editors of MEDICINE. Because this article does not involve any human or animal trials, there is no need to conduct special ethic review and the ethical approval is not necessary.When surgically treated, her specimen revealed a typical histopathology pattern of schwannoma. The patient's symptoms improved a lot after surgery and he continues to be under observation.Despite its rarity, intrasellar schwannoma should be considered in the differential diagnosis of sellar lesions that mimic pituitary adenomas.
机译:在中枢神经系统中,神经鞘瘤是无处不在的肿瘤,主要起源于听觉神经和三叉神经等感觉神经。然而,鞍内神经鞘瘤极少见。它们经常被误诊为垂体腺瘤。我们报告了一个在鞍区少见的神经鞘瘤病例,这是在临床表现,放射学迹象和术后病理检查的指导下极具挑战性的诊断。我们代表一名65岁的妇女,她患有头痛,甲状腺功能减退和视觉障碍。她的MRI显示异常的蝶鞍区混合信号肿块,伴鞍骨上,左侧鞍旁和蝶鞍底浸润。我们对患者的病程进行详细分析,并复习相关文献。从患者那里获得了书面知情同意,以发表本文。书面同意书的副本可供MEDICINE的编辑审查。由于本文不涉及任何人类或动物试验,因此无需进行特殊的伦理审查,也无需道德的认可。经过手术治疗后,她的标本揭示了典型的神经鞘瘤的组织病理学模式。手术后患者的症状已有很大改善,并且仍在继续观察。尽管罕见,但在模拟垂体腺瘤的鞍状病变的鉴别诊断中应考虑使用鞍内神经鞘瘤。

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