Reverse Trans-Sellar Neuroendoscopic Management of a Large Rathke’s Cleft Cyst Causing Obstructive Hydrocephalus: A Case Report

Symptomatic Rathke’s cleft cysts (RCCs) can be treated by surgical procedures, usually through an endonasal transsphenoidal corridor using either a microscope or an endoscope. We report a large suprasellar extended RCC causing obstructive hydrocephalus, which was efficiently managed by a novel surgical route named “reverse” trans-sellar approach using transventricular neuroendoscopy. A 48-year-old woman complained of persistent headache and a tendency to fall that had begun 6 months previously. The images obtained from MRI scan showed intra- and supra-sellar cystic masses occupying the third ventricle with obstruction of the foramina of Monro and the aqueduct of Sylvius. The cystic wall showed a slight enhancement, and the cystic contents showed iso-signal intensity on T1-and T2-weighted images. Instead of trans-nasal trans-sellar surgery, we decided to operate using a conventional transventricular endoscope. A thin cystic capsule, which blocked the foramina of Monro and the aqueduct of Sylvius, was fenestrated and removed and a third ventriculostomy was performed. The defect in the infundibulum between sellar and suprasellar cysts was widened and used as a corridor to drain cystic contents (reverse trans-sellar route). The final pathological finding revealed an RCC with focal metaplasia. We efficiently managed a large RCC by transventricular neuroendoscopic surgery with cyst fenestration and third ventriculostomy and simultaneously drained the sellar contents using a novel surgical route. Reverse trans-sellar neuroendoscopic surgery is a relevant treatment option for selective patients with large suprasellar extensions of RCCs.

[1]  T. Masumoto,et al.  Endoscopic endonasal cyst fenestration into the sphenoid sinus using the mucosa coupling method for symptomatic Rathke's cleft cyst: a novel method for maintaining cyst drainage to prevent recurrence. , 2019, Journal of neurosurgery.

[2]  Y. Hayashi,et al.  Entirely Suprasellar Rathke Cleft Cysts: Clinical Features and Surgical Efficacy of Endoscopic Endonasal Transtuberculum Sellae Approach. , 2019, World neurosurgery.

[3]  S. Manjila,et al.  Intratumoral Rathke's Cleft Cyst Remnants Within Craniopharyngioma, Pituitary Adenoma, Suprasellar Dermoid, and Epidermoid Cysts: A Ubiquitous Signature of Ectodermal Lineage or a Transitional Entity? , 2018, Neurosurgery.

[4]  S. Qi,et al.  The Supraorbital Keyhole Approach to the Suprasellar and Supra-Intrasellar Rathke Cleft Cysts Under Pure Endoscopic Visualization. , 2016, World neurosurgery.

[5]  T. Tominaga,et al.  Spontaneous Alteration from Rathke’s Cleft Cyst to Craniopharyngioma—Possible Involvement of Transformation Between These Pathologies , 2014, Endocrine Pathology.

[6]  I. El-Sayed,et al.  Extended endoscopic endonasal approach for suprasellar Rathke’s cleft cysts , 2014, Journal of Clinical Neuroscience.

[7]  M. Aghi,et al.  Rathke’s cleft cysts: review of natural history and surgical outcomes , 2014, Journal of Neuro-Oncology.

[8]  N. Karavitaki,et al.  Rathke’s cleft cysts , 2012, Clinical endocrinology.

[9]  F. Meyer,et al.  Symptomatic Rathke cleft cysts: extent of resection and surgical complications. , 2011, Neurosurgical focus.

[10]  Tao Xie,et al.  Endoscopic endonasal resection of symptomatic Rathke cleft cysts , 2011, Journal of Clinical Neuroscience.

[11]  S. Melmed,et al.  Pituitary magnetic resonance imaging for sellar and parasellar masses: ten-year experience in 2598 patients. , 2011, The Journal of clinical endocrinology and metabolism.

[12]  P. Gardner,et al.  Endoscopic endonasal resection of Rathke cleft cysts: clinical outcomes and surgical nuances. , 2010, Journal of neurosurgery.

[13]  L. Zou,et al.  Rathke's cleft cyst: clinicopathological and MRI findings in 22 patients. , 2010, Clinical radiology.

[14]  V. Zelman,et al.  Surgical outcomes in 118 patients with Rathke cleft cysts. , 2005, Journal of neurosurgery.

[15]  D. Mazzatenta,et al.  Transsphenoidal Endoscopic Approach in the Treatment of Rathke’s Cleft Cyst , 2005, Neurosurgery.

[16]  T. Naidich,et al.  Surgery for Rathke cleft cysts: technical considerations and outcomes. , 2004, Journal of neurosurgery.

[17]  K. Tabuchi,et al.  Neuroendoscopic transventricular surgery for suprasellar cystic mass lesions such as cystic craniopharyngioma and Rathke cleft cyst. , 2004, Neurologia medico-chirurgica.

[18]  J. Chi,et al.  Surgical treatment of symptomatic Rathke cleft cysts: clinical features and results with special attention to recurrence. , 2004, Journal of neurosurgery.

[19]  Hidenori Kobayashi,et al.  Clinical features of symptomatic Rathke's cleft cyst , 2001, Clinical Neurology and Neurosurgery.

[20]  S. Asa,et al.  Cystic lesions of the pituitary: clinicopathological features distinguishing craniopharyngioma, Rathke's cleft cyst, and arachnoid cyst. , 1999, The Journal of clinical endocrinology and metabolism.

[21]  H. J. Nepper-Rasmussen,et al.  Rathke's Cleft Cyst , 1996, Acta radiologica.

[22]  W. K. Chong,et al.  Cyst formation of the craniopharyngeal duct. , 1994, Clinical radiology.

[23]  J. Muller,et al.  Clinical, radiographic, and pathological features of symptomatic Rathke's cleft cysts. , 1991, Journal of neurosurgery.

[24]  Y. Takei,et al.  Symptomatic Rathke's cleft cysts located entirely in the suprasellar region: review of diagnosis, management, and pathogenesis. , 1985, Neurosurgery.