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dc.creatorKontogeorgos G., Thodou E., Osamura R.Y., Lloyd R.V.en
dc.date.accessioned2023-01-31T08:44:03Z
dc.date.available2023-01-31T08:44:03Z
dc.date.issued2022
dc.identifier10.1007/s42000-021-00333-y
dc.identifier.issn11093099
dc.identifier.urihttp://hdl.handle.net/11615/75082
dc.description.abstractHigh-risk pituitary adenomas are aggressive. They show clinical and imaging features similar to those of carcinomas, including infiltration of the surrounding brain structures, but lack cerebrospinal or systemic metastases. In addition, they display distinct behavior, including tendency for fast growth and frequent recurrences, which are difficult to control. The term “high-risk” adenoma was first introduced in the 4th edition of the World Health Organization Classification of Endocrine Tumors in 2017. Five defined adenoma types belong to this category, including sparsely granulated somatotroph, lactotroph in men, Crooke cell, silent corticotroph, and plurihormonal PIT-1 positive adenomas. The morphological and immunohistochemical characteristics of high-risk adenomas are herein described in detail. In addition, the clinical features and the treatment options are presented. This review focuses on predictive markers assessed by immunohistochemistry, which help clinicians to design the appropriate treatment strategies for high-risk adenomas. Somatostatin receptor status predicts effectiveness of postsurgical treatment with somatostatin analogs, and MGMT expression predicts response to treatment with temozolomide. This comprehensive review presents the clinical and pathological features of high-risk pituitary adenomas, underlines the contribution of immunohistochemistry, and emphasizes the leading role of pathology in the design of optimal clinical management. © 2021, Hellenic Endocrine Society.en
dc.language.isoenen
dc.sourceHormonesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85123234935&doi=10.1007%2fs42000-021-00333-y&partnerID=40&md5=738014e81953bf8f6cea9cc6bc91e898
dc.subjectcytokeratinen
dc.subjectepidermal growth factor receptoren
dc.subjectgrowth hormoneen
dc.subjectmessenger RNAen
dc.subjectpasireotideen
dc.subjectprogrammed death 1 receptoren
dc.subjectsomatostatinen
dc.subjectsomatostatin derivativeen
dc.subjectsomatostatin receptoren
dc.subjecttemozolomideen
dc.subjecttetradecapeptideen
dc.subjectvasculotropinen
dc.subjectACTH secreting adenomaen
dc.subjectACTH secreting cellen
dc.subjectadulten
dc.subjectcancer recurrenceen
dc.subjectclinical featureen
dc.subjectcontrast enhancementen
dc.subjectcontrolled studyen
dc.subjectCrooke cell adenomaen
dc.subjectgrowth hormone secreting adenomaen
dc.subjectgrowth hormone secreting cellen
dc.subjecthigh risk patienten
dc.subjecthistopathologyen
dc.subjecthumanen
dc.subjecthypophysis adenomaen
dc.subjectimmunohistochemistryen
dc.subjectimmunoreactivityen
dc.subjectmaleen
dc.subjectmetastasisen
dc.subjectmorbidityen
dc.subjectmortalityen
dc.subjectnuclear magnetic resonance imagingen
dc.subjectprevalenceen
dc.subjectprolactin secreting cellen
dc.subjectprotein synthesisen
dc.subjectradiomicsen
dc.subjectreal time reverse transcription polymerase chain reactionen
dc.subjectReviewen
dc.subjectT2 weighted imagingen
dc.subjecttreatment responseen
dc.subjecttumor associated leukocyteen
dc.subjecttumor growthen
dc.subjectWorld Health Organizationen
dc.subjectyoung adulten
dc.subjectadenomaen
dc.subjectcarcinomaen
dc.subjecthypophysis tumoren
dc.subjectimmunotherapyen
dc.subjectAdenomaen
dc.subjectCarcinomaen
dc.subjectHumansen
dc.subjectImmunohistochemistryen
dc.subjectImmunotherapyen
dc.subjectMaleen
dc.subjectPituitary Neoplasmsen
dc.subjectSpringer Science and Business Media Deutschland GmbHen
dc.titleHigh-risk pituitary adenomas and strategies for predicting response to treatmenten
dc.typeotheren


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