Intrasellar Cephalocele.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 33385601.
- Also identified by DOI 10.1016/j.wneu.2020.12.112.
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Abstract
Intrasellar cephalocele is very rare and is often overlooked because of its atypical clinical demonstration. A 2-year, 10-month-old girl was referred to our hospital with short stature. Magnetic resonance imaging revealed an extension of the anterior third ventricle, which protruded into the pituitary fossa, but not into the craniopharyngeal canal, sphenoid bone, or sphenoid sinus. In addition, there was no bony defect of the floor of the sellar turcica or the sphenoid sinus, and the mass was not protruding into the nasal cavity or nasopharynx. Thus the patient was clinically diagnosed with intrasellar cephalocele, which is considered as a rare subtype of transsphenoidal cephalocele. Instead of surgical intervention, the patient was given growth hormone replacement therapy. After 1-year follow-up, the patient had significant increase in height.
Medical subject headings
- Encephalocele
- Growth Disorders
- Human Growth Hormone
- Hypopituitarism
- Sella Turcica