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Chiloiro, S., Giampietro, A., Bianchi, A. and De Marinis, L. (2021) Empty Sella Syndrome: Multiple Endocrine Disorders. Handbook of Clinical Neurology, 181, 29-40.
https://doi.org/10.1016/B978-0-12-820683-6.00003-8

has been cited by the following article:

• TITLE: Sellar Arachnoidocele: An Unusual Evolution in a Case Report

  AUTHORS: Loubna Saadaoui, Sara Kebabi, Chaimaa Nahi, Zineb Tnacheri Ouazzani, Zineb Imane

  KEYWORDS: Sellar Arachnoidocele, GH Deficiency, Growth Hormone, Prognosis

  JOURNAL NAME: Open Journal of Clinical Diagnostics, Vol.12 No.4, December 15, 2022

  ABSTRACT: The sellar archnoidocele is a herniation of the subarachnoid space within the sella turcica which is often associated with a variable degree of flattening of the pituitary. Its clinical presentations range from an asymptomatic radiological finding to endocrine and neuro-ophthalmological manifestations. Its management depends on the initial symptomatology and requires long-term follow-up. We report here the case of a young child followed for a statural delay on a GH deficiency secondary to a sellar arachnoidocele, and who presents a rather unusual evolution.