- The Endocrinological Characteristics of Rathke's Cleft Cyst: Pathologically Confirmed in Seven Cases.
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Su Kyong Yu, Yun Kyung Kim, Hye Jin Kim, Dae Jung Kim, Yoon Sok Chung, Kwan Woo Lee, Se Hyuk Kim, Kyung Gi Cho
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J Korean Endocr Soc. 2007;22(1):74-79. Published online February 1, 2007
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DOI: https://doi.org/10.3803/jkes.2007.22.1.74
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 Abstract
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- Rathke's cleft cyst is a cystic sellar or suprasellar lesion thought to originate from the remnants of Rathke's pouch. It is characteristically lined by a single layer of ciliated cuboidal or columnar epithelium. Although small asymptomatic Rathke's cleft cysts have been reported at autopsy in 2~26% of normal pituitary glands, symptomatic cysts are rare. For patients with symptomatic Rathke's cleft cysts presentation with headache, pituitary dysfunction, and visual loss caused by compression of the optic chiasm in the event of suprasellar extension, is common. We report the endocrine characteristics of seven cases of patients with symptomatic Rathke's cleft cyst diagnosed with pathologic confirmation.
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Citations
Citations to this article as recorded by  - Risk factor for pituitary dysfunction in children and adolescents with Rathke's cleft cysts
Han Hyuk Lim, Sei Won Yang
Korean Journal of Pediatrics.2010; 53(7): 759. CrossRef
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