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Cysts of sellar and pharyngeal hypophyses.

作者信息

McGrath P

出版信息

Pathology. 1971 Apr;3(2):123-31. doi: 10.3109/00313027109071331.

DOI:10.3109/00313027109071331
PMID:5094869
Abstract
摘要

相似文献

1
Cysts of sellar and pharyngeal hypophyses.
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Anatomico-radiological study of the borderline sella.
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Empty sella syndrome secondary to intrasellar cyst in adolescence.青春期继发于鞍内囊肿的空蝶鞍综合征。
Am J Dis Child. 1976 Sep;130(9):1009-12. doi: 10.1001/archpedi.1976.02120100099017.
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Atypical CT and MR appearance of a Rathke cleft cyst.Rathke裂囊肿的非典型CT和MR表现。
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The pathologic, surgical, and MR spectrum of Rathke cleft cysts.
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Sellar tuberculoma: report of two cases.
Acta Neurochir (Wien). 1997;139(6):523-5. doi: 10.1007/BF02750994.
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Arachnoid cysts in the hypophyseal area.
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10
Sellar tuberculoma.鞍区结核瘤
J Neurol Neurosurg Psychiatry. 1992 Jul;55(7):629. doi: 10.1136/jnnp.55.7.629-a.

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Growth dynamics of Rathke's Cleft cyst: a risk score system for surgical decision making.Rathke's 裂隙囊肿的生长动力学:手术决策的风险评分系统。
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Rathke Cleft Cyst with Occulomotor Palsy: An Unusual Presentation.伴有动眼神经麻痹的拉克囊肿:一种罕见表现
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T2 hypointense signal discovered incidentally at the posterior edge of the adenohypophysis on MRI: its prevalence and morphology and their relationship to age.
MRI 偶然发现的腺垂体后缘 T2 低信号:其发生率、形态及其与年龄的关系。
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Endonasal Endoscopic Fenestration of Rathke's Cleft Cysts: Whether to Leave the Fenestration Open or Closed?经鼻内镜下Rathke裂囊肿开窗术:开窗应开放还是封闭?
J Neurol Surg B Skull Base. 2021 Jul;82(Suppl 3):e101-e104. doi: 10.1055/s-0039-3402042. Epub 2019 Dec 23.
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Rathke's Cleft Cyst or Pituitary Apoplexy: A Case Report and Literature Review.拉克氏裂囊肿或垂体卒中:一例报告及文献综述
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PLoS One. 2016 Mar 7;11(3):e0151080. doi: 10.1371/journal.pone.0151080. eCollection 2016.
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Rathke's cleft cysts: review of natural history and surgical outcomes.拉克氏裂囊肿:自然史与手术结果综述
J Neurooncol. 2014 Apr;117(2):197-203. doi: 10.1007/s11060-013-1272-6. Epub 2013 Oct 22.
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MR imaging findings of Rathke's cleft cysts: significance of intracystic nodules.拉克氏囊肿的磁共振成像表现:囊内结节的意义
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CT findings in symptomatic Rathke's cleft cysts of the pituitary gland. Report of three cases.
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