Kleinschmidt-DeMasters B K, Lillehei K O, Stears J C
Department of Pathology, University of Colorado Health Sciences Center, Denver 80262, USA.
Surg Neurol. 1995 Jul;44(1):19-26; discussion 26-7. doi: 10.1016/0090-3019(95)00144-1.
Rathke cleft cysts (RCC) uncommonly attain large enough size to cause symptoms or warrant neurosurgical intervention, leading to difficulty in recognizing their diverse presentations.
We retrospectively reviewed the clinical, intraoperative, pathologic, and magnetic resonance (MR) imaging findings of 16 cases seen at our institution since 1987.
The most unusual clinical presentation was pituitary apoplexy, although CSF-like, cholesterol containing, or hemorrhagic cyst contents most often led to intraoperative misinterpretation. Microscopic features of squamous metaplasia, lymphocytic infiltrates, tubuloracemose glands, or coexistent adenomas demonstrated the pathologic variations in these intrasellar and suprasellar cysts. The MR findings of an anteriorly displaced pituitary stalk, the presence of a posterior ledge, and T2 hypointensity were distinctive, when present.
Rathke cleft cysts have varied clinical presentations and sometimes confusing intraoperative and pathologic appearances. We document a new pathognomonic MR finding in these cysts of a posterior ledge sign. Our surgical approach is to open and drain cyst contents, treat the residual cyst lining with instillation of absolute alcohol, and close the floor of the sella with a bone strut.
