| Literature DB >> 6828994 |
D Rout, L Das, V R Rao, V V Radhakrishnan.
Abstract
Two unusual cases of symptomatic Rathke's cleft cysts are reported. In one, the cyst was entirely suprasellar with a normal sella turcica. The gross visual failure, hypothalamic disturbances, and hypopituitarism of the patient resolved after a transfrontal aspiration and partial excision of the wall of the cyst. The second patient was a pituitary dwarf with hypothalamic dysfunction, but with normal vision. The patient had a large intrasellar cyst that exhibited marked suprasellar extension with calcification of the capsular rim. After transsphenoidal aspiration and partial excision of the wall of the cyst, the patient achieved a satisfactory recovery. The differential features between Rathke's cleft cyst and craniopharyngioma are highlighted.Entities:
Mesh:
Year: 1983 PMID: 6828994 DOI: 10.1016/0090-3019(83)90209-4
Source DB: PubMed Journal: Surg Neurol ISSN: 0090-3019