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dc.contributor.authorLocatelli D.
dc.contributor.authorVeiceschi P.
dc.contributor.authorCastelnuovo P.
dc.contributor.authorTanriover N.
dc.contributor.authorEvliyaoglu O.
dc.contributor.authorCanaz H.
dc.contributor.authorGazioglu N.
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:52:48Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:52:48Z
dc.date.issued2019
dc.identifier.issn0256-7040
dc.identifier.urihttps://dx.doi.org/10.1007/s00381-019-04179-z
dc.identifier.urihttp://hdl.handle.net/11446/1733
dc.description.abstractIntroduction: Pediatric pituitary adenomas are rare lesions. Incidence is reported between 1 and 10% of all childhood brain tumors and between 3 and 6% of all surgically treated adenomas. Although pituitary adenomas present with symptoms of hormone hypersecretion or neurological disruptions secondary to mass effect, they are almost constantly benign. Characteristics of patients may vary in different studies according to age, gender, size of adenoma, hormonal activity, and recurrence rates. Methods: Data on consecutive pediatric patients who were operated for pituitary adenoma with endoscopic endonasal transsphenoidal surgery (EETS) and transsphenoidal microsurgery (TMS) in the Department of Neurosurgery, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey, in the Neurosurgical Unit of the San Matteo Hospital, Pavia, Italy, and in the Division of Neurological Surgery Department of Biotechnology and Life Sciences, University of Insubria-Varese, ASST Sette Laghi, Ospedale di Circolo e Fondazione Macchi, Varese, Italy, between July 1997 and May 2018, were analyzed. Twenty-seven patients (11 males and 16 females), who were 18 years old or younger at the time of surgery, were included in the study. Medical records, images, and operative notes of patients were retrospectively reviewed. Results: There were 16 females (59.3%) and 11 males (40.7%). Mean age was 15.3 ± 3.3 (4–18). Thirty-two surgical procedures were performed for 27 patients (6 children required second operation). Thirteen patients (48.14%) had Cushing’s disease (CD), 5 patients (18.5%) had growth hormone (GH)-secreting adenoma, 5 patients (18.5%) had prolactinoma, and 4 patients (14.8%) had non-functional adenoma. Twenty-two patients (81.4%) met remission criteria, and 5 patients (18.5%) did not meet remission criteria. Four patients met remission criteria after the second operation. Conclusion: Transsphenoidal approach affords effective release of mass effect and not only restoration but also perpetuation of normal endocrine functions in the majority of pediatric pituitary adenoma patients. Satisfactory results are reported with both EETS and TMS in the literature. Despite the technical difficulties in pediatric age, transsphenoidal resection of adenoma is still the mainstay treatment that provides cure in pediatric patients. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.en_US
dc.language.isoengen_US
dc.publisherSpringer Verlagen_US
dc.identifier.doi10.1007/s00381-019-04179-zen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEndoscopic endonasal transsphenoidal surgeryen_US
dc.subjectOutcomeen_US
dc.subjectPediatric pituitary adenomasen_US
dc.subjectRemissionen_US
dc.subjectSkull baseen_US
dc.subjectTranssphenoidal microsurgeryen_US
dc.titleTranssphenoidal surgery for pituitary adenomas in pediatric patients: a multicentric retrospective studyen_US
dc.typearticleen_US
dc.relation.journalChild's Nervous Systemen_US
dc.departmentDBÜen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempDBÜen_US


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