Rathke pouch cyst

Quiste de la bolsa de Rathke

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William Rojas García
Sebastian Herrera Acero
Natalia Andrea González Macias

Abstract

Rathke pouch cysts are epithelium-lined cysts arising from the embryological remnants of Rathke´s pouch. They are usually incidentally identified since the majority are asymptomatic. They become symptomatic when they enlarge enough to compress neighbor structures causing headache, visual disturbances and pituitary dysfunction. They occur mostly in adults in the fourth to fifth decades of life. A case is presented in a 9-year-old female patient who consulted for growth retardation to the endocrinology service. She was treated with growth hormone and a magnetic resonance imaging (MRI) scan reported Rathke´s pouch cyst versus pituitary adenoma.

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Author Biographies

William Rojas García, Fundación Universitaria de Ciencias de la Salud

Servicio de Endocrinología Hospital de San José, Fundación Universitaria de Ciencias de la Salud.
Bogotá DC, Colombia

Sebastian Herrera Acero, Fundación Universitaria Ciencias de la Salud

Medicina, Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia

Natalia Andrea González Macias, Fundación Universitaria Ciencias de la Salud

Medicina, Fundación Universitaria de Ciencias de la Salud. Bogotá DC, Colombia

References

Larkin S, Karavitaki N, Ansorge O. Rathke's cleft cyst. Handbook of clinical neurology. 2014;124:255-69. doi: 10.1016/B978-0-444-59602-4.00017-4.

Uppal S, Jee YH, Lightbourne M, Han JC, Stratakis CA. Combined pituitary hormone deficiency in a girl with 48, XXXX and Rathke's cleft cyst. Hormones (Athens). 2017;16(1):92-8. doi: 10.14310/horm.2002.1723.

Jung JE, Jin J, Jung MK, Kwon A, Chae HW, Kim DH, et al. Clinical manifestations of Rathke's cleft cysts and their natural progression during 2 years in children and adolescents. Annals of pediatric endocrinology & metabolism. 2017;22(3):164-9. doi: 10.6065/apem.2017.22.3.164.

Esparza Estaún J, Elduayen Aldaz B, de Arriba Villamor C. Estudio por Resonancia Magnética del eje hipotálamo-hipofisario en pediatría. Rev Esp Endocrinol Pediatr. 2013;4(Suppl):101-5. doi: 10.3266/RevEspEndocrinolPediatr.pre2013.Mar.174

Mendelson ZS, Husain Q, Elmoursi S, Svider PF, Eloy JA, Liu JK. Rathke's cleft cyst recurrence after transsphenoidal surgery: a meta-analysis of 1151 cases. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 2014;21(3):378-85. doi: 10.1016/j.jocn.2013.07.008.

Shatri J, Ahmetgjekaj I. Rathke's Cleft Cyst or Pituitary Apoplexy: A Case Report and Literature Review. Open access Macedonian journal of medical sciences. 2018;6(3):544-7. doi: 10.3889/oamjms.2018.115.

Mrelashvili A, Braksick SA, Murphy LL, Morparia NP, Natt N, Kumar N. Chemical meningitis: a rare presentation of Rathke's cleft cyst. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 2014;21(4):692-4.

Han SJ, Rolston JD, Jahangiri A, Aghi MK. Rathke's cleft cysts: review of natural history and surgical outcomes. Journal of neuro-oncology. 2014;117(2):197-203. doi: 10.1007/s11060-013-1272-6.

Hirayama Y, Kudo T, Kasai N. Acute Adrenal Insufficiency Associated with Rathke's Cleft Cyst. Intern Med. 2016;55(6):639-42. doi: 10.2169/internalmedicine.55.4803.

Rumboldt Z, Castillo M, Huang B, Rossi A. Brain imaging with MRI and CT. An image pattern approach. Elsevier: Cambridge University Press; 2010. p. 79-80.

Culver SA, Grober Y, Ornan DA, Patrie JT, Oldfield EH, Jane JA, Jr., et al. A Case for Conservative Management: Characterizing the Natural History of Radiographically Diagnosed Rathke Cleft Cysts. The Journal of clinical endocrinology and metabolism. 2015;100(10):3943-8. doi: 10.1210/jc.2015-2604.

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