ISSN: 1308-5727 | E-ISSN: 1308-5735
Volume: 16 Issue: 4 Year: 2024
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Turkish Society for Pediatric Endocrinology and Diabetes
Extensive Middle Cranial Fossa Arachnoid Cysts and Different Clinical Presentation in Two Patients [J Clin Res Pediatr Endocrinol]
J Clin Res Pediatr Endocrinol. 2014; 6(3): 174-176 | DOI: 10.4274/jcrpe.1381

Extensive Middle Cranial Fossa Arachnoid Cysts and Different Clinical Presentation in Two Patients

Özge Yüce1, Esra Döğer1, Nurullah Çelik1, Hamdi Cihan Emeksiz1, Erkut Baha Bulduk2, Mahmut Orhun Çamurdan1, Aysun Bideci1, Peyami Cinaz1
1Gazi Univesity Faculty Of Medicine, Department Of Pediatric Endocrinology, Ankara, Turkey
2Gazi Univesity Faculty Of Medicine, Department Of Pediatric Neurosurgery, Ankara, Turkey

Arachnoid cysts (ACs), particularly suprasellar cysts, cause a wide spectrum of endocrine disorders. Herein, we report two patients diagnosed with an extensive AC in the middle cranial fossa while being investigated for etiologies of precocious puberty and short stature. One of them required surgery due to his pubertal disorders associated with compression effects of cyst. After surgery, his puberty progression was regressed within one year. On the other hand, surgery was not planned for the second patient considering of his cranial imaging findings and the extremely low incidence of growth hormone (GH) deficiency caused by middle fossa AC (MFAC). We started treatment with recombinant human GH and no complication was found during treatment follow-up. Endocrine disorders associated with MFACs are extremely rare. By presenting with these two cases, we aimed to remain our fellow physcians that ACs can be possibly cause of endocrine disorders. Clinicians should be careful evaluating endocrine disorders because real cause may not be cyst itself but masked by it.

Keywords: Extensive arachnoid cyst,Growth hormone deficiency,puberty precocious


Manuscript Language: English
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