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Primary choroid plexus papilloma in the pituitary fossa: case report and literature review

机译:垂体窝原发性脉络丛乳头状瘤:病例报告并文献复习

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摘要

Choroid plexus papillomas are rare tumors of the central nervous system and are usually confined to the ventricular system. We illustrated a primary choroid plexus papilloma in the pituitary fossa. A 31-year-old female presented with amenorrhea and intermittent galactorrhoea, with no visual complaints in the last 2 years. Endocrine testing showed no hormone excess or deficiency of the pituitary and target glands, except for a higher prolactin level (56 ng/ml). A sharply circumscribed regular mass in the sellar region occupying the entire sella turcica and extending into the suprasellar cistern was demonstrated on MR imaging with gadolinium diethylenetriamine pentaacetic acid. The patient underwent an endonasal trans-sphenoidal approach. Complete microsurgical excision and complete preservation of the normal pituitary gland was achieved, with normal prolactin level. The histopathology showed that the lesion was a choroid plexus papilloma. Theories of the origin, the differential diagnosis, and treatment of the rare tumor are discussed.
机译:脉络丛乳头状瘤是中枢神经系统的罕见肿瘤,通常局限于心室系统。我们图示了垂体窝中的原发性脉络膜丛乳头状瘤。一名31岁的女性出现闭经和间歇性半乳痛,在过去的两年中无视觉不适。内分泌测试表明,除了较高的催乳素水平(56 ng / ml)外,垂体和靶腺均无激素过量或不足。用with二亚乙基三胺五乙酸进行MR成像显示,在蝶鞍区域中明显划定的规则肿块占据了整个蝶鞍水槽并延伸到鞍上水箱。该患者接受了鼻内蝶窦入路。完整的显微手术切除和正常垂体的完整保存,泌乳素水平正常。组织病理学显示该病变为脉络丛乳头状瘤。讨论了罕见肿瘤的起源,鉴别诊断和治疗的理论。

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