Extensive middle cranial fossa arachnoid cysts and different clinical presentation in two patients

J Clin Res Pediatr Endocrinol. 2014 Sep;6(3):174-6. doi: 10.4274/Jcrpe.1381.

Abstract

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.

Publication types

  • Case Reports

MeSH terms

  • Arachnoid Cysts / complications
  • Arachnoid Cysts / diagnosis*
  • Arachnoid Cysts / therapy
  • Biomarkers / blood
  • Child
  • Cranial Fossa, Middle* / drug effects
  • Cranial Fossa, Middle* / pathology
  • Cranial Fossa, Middle* / surgery
  • Decompression, Surgical
  • Growth Disorders / etiology
  • Hormone Replacement Therapy
  • Human Growth Hormone / blood
  • Human Growth Hormone / deficiency
  • Human Growth Hormone / therapeutic use
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Puberty, Precocious / etiology
  • Treatment Outcome

Substances

  • Biomarkers
  • Human Growth Hormone