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Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Suprasellar and recurrent pediatric craniopharyngiomas: expanding indications for the extended endoscopic
Andrew F Alalade1, Elizabeth Ogando-Rivas1, Jerome Boatey1
1Departments of1Neurosurgery.
Insights
The endoscopic transsphenoidal approach is effective for pediatric craniopharyngiomas, even in young children and complex cases. This minimally invasive technique allows for safe tumor removal, though endocrinopathy rates remain high.
Area of Science:
- Neurosurgery
- Pediatric Oncology
- Endoscopic Surgery
Background:
- Craniopharyngiomas are rare pediatric brain tumors.
- The endonasal endoscopic transsphenoidal approach (EETSA) is increasingly used but concerns exist for young children, recurrent tumors, and suprasellar masses.
- Traditional limitations include narrow corridors and fear of hypothalamic injury.
Purpose of the Study:
- To evaluate the utility and safety of the EETSA for pediatric craniopharyngiomas across varied patient ages, tumor locations, and treatment histories.
- To reassess traditional concerns regarding the limitations of the EETSA in pediatric craniopharyngioma surgery.
Main Methods:
- A retrospective review of 11 consecutive pediatric patients (age ≤ 18 years) who underwent EETSA for craniopharyngioma between 2007 and 2016.
- Data collected included tumor characteristics, extent of resection, and postoperative outcomes (visual, endocrine, weight, academic return).
- Radiographic assessment of hypothalamic invasion and skull base measurements were performed.
Main Results:
- Gross-total resection was achieved in 45% of patients, irrespective of tumor location, consistency, or patient age.
- Postoperative anterior pituitary dysfunction occurred in 81.8%, and diabetes insipidus in 63.3%.
- Visual function improved or remained stable in 73%, and all patients returned to school.
Conclusions:
- The EETSA is a viable option for pediatric craniopharyngiomas, including in young children, suprasellar tumors, and recurrent cases.
- Tumor invasiveness, not the surgical approach, dictates the extent of resection.
- While effective, the approach necessitates careful consideration of high rates of postoperative endocrinopathy and a steep learning curve.
Abstract:
OBJECTIVE The expanded endonasal endoscopic transsphenoidal approach has become increasingly used for craniopharyngioma surgery in the pediatric population, but questions still persist regarding its utility in younger children, in recurrent and irradiated tumors, and in masses primarily located in the suprasellar region. The narrow corridor, incomplete pneumatization, and fear of hypothalamic injury have traditionally relegated this approach to application in older children with mostly cystic craniopharyngiomas centered in the sella. The authors present a series of consecutive pediatric patients in whom the endonasal endoscopic approach was used to remove craniopharyngiomas from patients of varied ages, regardless of the location of the tumor and previous treatments or surgeries, to ascertain if the traditional concerns about limitations of this approach are worth reevaluating METHODS Eleven consecutive pediatric patients (age ≤ 18 years) underwent surgery via an endoscopic transsphenoidal approach at NewYork-Presbyterian/Weill Cornell Medical Center from 2007 to 2016. The authors recorded the location, consistency, and size of the lesion, assessed for hypothalamic invasion radiographically, calculated skull base measurements, and assessed parameters such as extent of resection, visual function, endocrinological function, weight gain, and return-to-school status. RESULTS The average age at the time of surgery was 7.9 years (range 4-17 years) and the tumor sizes ranged from 1.3 to 41.7 cm3. Five cases were purely suprasellar, 5 had solid components, 4 were reoperations, and 5 had a conchal sphenoid aeration. Nevertheless, gross-total resection was achieved in 45% of the patients and 50% of those in whom it was the goal of surgery, without any correlation with the location, tumor consistency, or the age of the patient. Near-total resection, subtotal resection, or biopsy was performed intentionally in the remaining patients to avoid hypothalamic injury. Anterior pituitary dysfunction occurred in 81.8% of the patients, and 63.3% developed diabetes insipidus . Two patients (18%) had a greater than 9% increase in body mass index. Visual function was stable or improved in 73%. All children returned to an academic environment, with 10 of them in the grade appropriate for their age. There was a single case of each of the following: CSF leak, loss of vision unilaterally, and abscess. CONCLUSIONS The endoscopic transsphenoidal approach is suitable for removing pediatric craniopharyngiomas even in young children with suprasellar tumors, conchal sphenoid sinus, recurrent tumors, and tumors with solid components. The extent of resection is dictated by intrinsic hypothalamic tumor invasiveness rather than the approach. The endoscopic transsphenoidal approach affords the ability to directly inspect the hypothalamus to determine invasion, which may help spare the patient from hypothalamic injury. Irrespective of approach, the rates of postoperative endocrinopathy remain high and the learning curve for the approach to a relatively rare tumor is steep.

