Ann Pediatr Endocrinol Metab.  2014 Mar;19(1):20-26. 10.6065/apem.2014.19.1.20.

Clinical and radiological findings of incidental Rathke's cleft cysts in children and adolescents

Affiliations
  • 1Department of Pediatrics, Hallym University College of Medicine, Seoul, Korea. ithwang83@hallym.or.kr
  • 2Department of Neurosurgery, Hallym University College of Medicine, Seoul, Korea.

Abstract

PURPOSE
In the pediatric population, Rathke's cleft cysts (RCCs) are known to be an infrequent cause of headaches, visual disturbances, and pituitary dysfunction. We investigated the clinical characteristics of children in whom RCCs were incidentally discovered and evaluated whether RCCs influence the treatment response of patients with proven endocrinopathy.
METHODS
A retrospective analysis was conducted in 34 patients with RCCs who were diagnosed between 2006 and 2013 at Hallym University Medical Center. Their clinical, hormonal, and imaging findings were reviewed. We evaluated the clinical outcomes of the patients with concomitant RCCs and endocrinopathy compared to matched controls.
RESULTS
Twenty-six of 34 patients with radiologically proven RCCs had endocrine disorders. They were 9 boys and 17 girls, with ages ranging from 4.8 to 17.4 years at the time of the diagnosis. Of these, 7 (27%) had idiopathic short stature, 7 (27%) had growth hormone deficiency (GHD), and 12 (46%) had central precocious puberty (CPP). Nineteen of 26 patients (73.1%) showed low signal intensities on T1-weighted images (T1WI) and high signal intensities on T2-weighted images. The incidence of hypointensity on T1WI was higher in the patients with RCCs accompanied by endocrinopathy than in those without endocrinopathy (P=0.033). The treatment outcomes of the patients with CPP and GHD with and without RCCs were similar.
CONCLUSION
CPP and GHD patients with a small RCC (less than 20 mm) expressing cystic magnetic resonance intensity can be managed with medical treatment, although the RCCs need to be closely monitored in radiological studies to observe their growth.

Keyword

Central nervous system cysts; Pituitary dwarfism; Precocious puberty; Central

MeSH Terms

Academic Medical Centers
Adolescent*
Central Nervous System Cysts*
Child*
Diagnosis
Dwarfism, Pituitary
Female
Growth Hormone
Headache
Humans
Incidence
Puberty, Precocious
Retrospective Studies
Growth Hormone

Cited by  1 articles

Clinical manifestations of Rathke’s cleft cysts and their natural progression during 2 years in children and adolescents
Jo Eun Jung, Juhyun Jin, Mo Kyung Jung, Ahreum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(3):164-169.    doi: 10.6065/apem.2017.22.3.164.


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