Silent corticotroph adenomas.

Silent corticotroph pituitary adenomas (SCA) are defined as pituitary adenomas showing positive staining for adrenocorticotrophic hormone in immunohistochemical studies, but not associated with perioperative clinical or laboratory features of hypercortisolaemia. They account for 1.1-6% of surgically...

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Main Authors: Karavitaki, N, Ansorge, O, Wass, J
Format: Journal article
Language:English
Published: 2007
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author Karavitaki, N
Ansorge, O
Wass, J
author_facet Karavitaki, N
Ansorge, O
Wass, J
author_sort Karavitaki, N
collection OXFORD
description Silent corticotroph pituitary adenomas (SCA) are defined as pituitary adenomas showing positive staining for adrenocorticotrophic hormone in immunohistochemical studies, but not associated with perioperative clinical or laboratory features of hypercortisolaemia. They account for 1.1-6% of surgically removed pituitary adenomas. Currently, two distinct pathologic subtypes of SCA are recognised. Their pathogenesis remains unclear. They present with local mass effects (headache, visual deterioration, cranial nerve palsies, endocrine dysfunction). The lack of manifestations of cortisol excess has not been conclusively explained. In surgical series, most tumours are macroadenomas with suprasellar extension present in 87-100% of the cases; this is in contrast to Cushing's disease, which is mostly attributed to microadenomas. Surgery remains the main therapeutic approach. Attempts to identify predictors of recurrence have not been successful. Management and follow-up protocols should be planned taking into account their potential aggressive behaviour, particularly upon recurrence. The development of florid pituitary Cushing's syndrome and local recurrence followed by metastatic disease (occasionally outside the central nervous system) have been rarely reported.
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spelling oxford-uuid:93c846fb-b38c-422a-a7c0-0301f988c0612022-03-26T23:34:35ZSilent corticotroph adenomas.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:93c846fb-b38c-422a-a7c0-0301f988c061EnglishSymplectic Elements at Oxford2007Karavitaki, NAnsorge, OWass, JSilent corticotroph pituitary adenomas (SCA) are defined as pituitary adenomas showing positive staining for adrenocorticotrophic hormone in immunohistochemical studies, but not associated with perioperative clinical or laboratory features of hypercortisolaemia. They account for 1.1-6% of surgically removed pituitary adenomas. Currently, two distinct pathologic subtypes of SCA are recognised. Their pathogenesis remains unclear. They present with local mass effects (headache, visual deterioration, cranial nerve palsies, endocrine dysfunction). The lack of manifestations of cortisol excess has not been conclusively explained. In surgical series, most tumours are macroadenomas with suprasellar extension present in 87-100% of the cases; this is in contrast to Cushing's disease, which is mostly attributed to microadenomas. Surgery remains the main therapeutic approach. Attempts to identify predictors of recurrence have not been successful. Management and follow-up protocols should be planned taking into account their potential aggressive behaviour, particularly upon recurrence. The development of florid pituitary Cushing's syndrome and local recurrence followed by metastatic disease (occasionally outside the central nervous system) have been rarely reported.
spellingShingle Karavitaki, N
Ansorge, O
Wass, J
Silent corticotroph adenomas.
title Silent corticotroph adenomas.
title_full Silent corticotroph adenomas.
title_fullStr Silent corticotroph adenomas.
title_full_unstemmed Silent corticotroph adenomas.
title_short Silent corticotroph adenomas.
title_sort silent corticotroph adenomas
work_keys_str_mv AT karavitakin silentcorticotrophadenomas
AT ansorgeo silentcorticotrophadenomas
AT wassj silentcorticotrophadenomas