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The clinical course of Rathke's cleft cysts in pediatric patients: impact on growth and pubertal development
Yousuke Higuchi1,2, Kosei Hasegawa3, Toshihide Kubo2
1Department of Pediatrics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Insights
Rathke's cleft cysts (RCCs) in children can cause growth issues and precocious puberty. Medical treatments, including hormone therapy, are often effective for managing associated endocrinopathy and cyst size.
Area of Science:
- Pediatric Endocrinology
- Neurosurgery
- Radiology
Background:
- Rathke's cleft cysts (RCCs) are sellar/suprasellar epithelial lesions.
- While often asymptomatic, RCCs can cause headaches, visual issues, and endocrine disorders.
- Optimal treatment for RCC-associated endocrinopathy is not well-defined.
Purpose of the Study:
- To analyze the clinical course, MRI findings, and treatment responses in pediatric patients with RCCs and endocrinopathy.
- To evaluate the efficacy of medical versus surgical interventions.
- To identify prevalent endocrine disturbances in this cohort.
Main Methods:
- Retrospective review of 10 pediatric patients with RCCs and endocrinopathy.
- Analysis of clinical data, magnetic resonance imaging (MRI) findings, and treatment outcomes.
- Assessment of hormonal levels and growth parameters.
Main Results:
- Growth impairment and precocious puberty were common findings.
- Seven of nine medically treated patients had stable cyst size; two showed reduction.
- Hormone replacement and gonadotropin suppression therapies were effective.
- One patient with suprasellar extension underwent surgery.
Conclusions:
- Medical management, including hormone therapy, is effective for pediatric RCCs with endocrinopathy.
- Regular imaging and endocrine monitoring are crucial due to potential changes.
- RCCs can present with diverse endocrine manifestations in children.
Abstract:
Rathke's cleft cysts (RCCs) are non-neoplastic epithelial lesions in the sellar or suprasellar regions. RCCs are usually asymptomatic; however, some patients experience headaches, visual disturbances, and endocrine disorders. The best treatment for associated endocrinopathy remains elusive. We aimed to investigate the clinical course, magnetic resonance imaging findings, and response to therapy in 10 pediatric patients with RCCs and endocrinopathy. Growth impairment and precocious puberty were observed to be prevalent. One patient with suprasellar extension of RCC underwent surgery, while the others were treated medically. Of the nine patients, seven patients showed stable cyst size, while two patients displayed reduction in cyst size. Hormone replacement and gonadotropin suppression therapy were found to be effective. Imaging and endocrine follow-ups are warranted because of the potential for changes in the cyst size and hormonal changes.
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