2013, Number 3
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Evid Med Invest Salud 2013; 6 (3)
Rathke cyst
Gutiérrez ARA, Romo BG, Pacheco UF
Language: Spanish
References: 22
Page: 95-99
PDF size: 622.48 Kb.
ABSTRACT
Rathke cleft cyst is a ectodemo’s invagination, due to de third and fourth weeks of pregnancy go to the estomodeo zone and made the adenohyphofisis. Rathke cyst is rare and represent minus of the 1% of all brain tumors. This cyst are seldom symptomatic, when made symptomatic is for compression, is common the headaches, diplopia and less vision. We made present a interesting case from man a 19 years old with the symptomatic classic for a big Rathke cyst.
REFERENCES
Shanklin WM. On the presence of cysts in the human pituitary. Anat Rec. 1949; 104: 379-407.
Frannk F, Sciarreta V, Mazzatenta D, Farneti G, Modugno GC, Pasquini E. Transsphenoidal endoscopic approach in the treatment of Rathke’s cleft cyst. Neurosurgery. 2005; 56: 124-29.
Megdiche-Bazarbacha H, Ben Hammouda K, Aicha AB, Sebai R et al. Intrasphenoidal Rathke cleft cyst. AJNR Am J Neuroradiol. 2006; 27: 1998-100.
Vancura RW, Jacob KM, Damjanov I. A 70 year old man with diplopia, nausea and vomiting. Rathke cleft cyst concomitant with pituitary adenoma. Arch Patol Lab Med. 2006; 130: 403-4.
Ng YT, Kerrigan FJ, Prenger EC, White WL, Rekate HL. Successful resection of the hipotalamic hamartoma and the Rathke cleft cyst. Case report. J Neurosurg. 2005; 102: 78-80.
Páramo F et al. Guía clínica del diagnóstico y tratamiento del craneofaringioma y otras lesiones paraselares. Endocrinol Nutr. 2007; 54 (1): 13-22.
Kasperbauer JL, Orvidas LJ, Atkinson JL, Abbound CF. Rathke cleft cyst: diagnostic and therapeutic considerations. Laryngoscope. 2002; 112: 1836-39.
Takanashi J, Tada H, Barkovich AJ, Saeki N, Kohono Y. Pituitary cyst in childhood evaluated by MR imaging. AJNR Am J Neurorradiol. 2005; 26: 2144-7.
Saleem SN, Said AH, Lee DH. Lesions of the hypothalamus: MR imaging diagnostic features. Radiogaphics. 2007; 27: 1087-1108.
Prayson RA, Goldblum JR. Neuropathology. 2005; Elsevier inc.
Langman J. Medical embriology. Baltimore: Williams & Wilkins; 1981.
Nemergut EC, Zuo Z, Jane JA Jr, Laws ER Jr. Predictors of diabetes insipidus after transsphenoidal surgery: a review of 881 patients. J Neurosurg. 2005; 103: 448-54.
Voelker JL, Campbell RL, Muller J. Clinical radiographics and pathological features of symptomatic Rathk’s cleft cyst. J Neurosurg. 1991; 74: 534-44.
Benveniste RJ, King WA, Walsh J, Lee JS, Naidich TP, Post KD. Surgery for Rathke cleft cyst: Technical considerations and outcomes. J Neurosurg. 2004; 101: 577-84.
Rao KCVG. Degenerative diseases and hydrocephalus. In: Lee SH, Rao KCVG, Zimmerman RA, editors. Cranial MRI and CT. 4th ed. New York: McGraw-Hill; 1999. pp. 212-214.
Kim JE, Kim JH, Kim OL, Paek SH, Kim DG, Chi JG, Jung HW. Surgical treatment of symtomatic Rathke cleft cysts: clinical features and results with special attention to recurrence. J Neurosurg. 2004; 100: 33-40.
Hayashi Y, Tachibana O, Muramatsu N, Tsuchiya H, Tada M, Arakawa Y et al. Rathke cleft cyst: MR and biomedical analysis of cyst content. J Comput Assist Tomogr. 1999; 23: 34-8.
Baskin DS. Wilson CB Transsphenoidal treatment of no neoplastic intrasellar cyst. A report of 38 cases. J Neurosurg. 1984; 60: 8-13.
Hitz RL. Management of craniopharingyoma. Acta Paediatr Suppl. 1996; 417: 81-2.
Hald JK, Eldevik OP, Skalpe IO. Craniopharingioma identification by CT and MR imaging at 1.5 T. Acta Radiol. 1995; 36: 142-7.
Aguirre-Cruz ML, Sotelo-Morales J. Tumores cerebrales. México: Médica Panamericana; 2008.
Karaviataki N, Brufani C, Warner JT, Adams CBT, Richards P, Ausosrge O et al. Craniopharingiomas in children and adults: systematic analysis of 121 cases with-long term follow-up. Clinical Endocrinol (Oxf). 2005; 62: 397-409.