Pituitary carcinoma: reclassification and implications in the NET schema

The entity known as pituitary carcinoma has been traditionally defined as a tumor of adenohypophysial cells that metastasizes systemically or craniospinally independent of the histological appearance of the lesion. Reported cases of pituitary carcinoma have clinically and histologically resembled th...

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Main Authors: Sylvia L Asa, Shereen Ezzat
Format: Article
Language:English
Published: Bioscientifica 2023-01-01
Series:Endocrine Oncology
Subjects:
Online Access:https://eo.bioscientifica.com/view/journals/eo/2/1/EO-22-0041.xml
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author Sylvia L Asa
Shereen Ezzat
author_facet Sylvia L Asa
Shereen Ezzat
author_sort Sylvia L Asa
collection DOAJ
description The entity known as pituitary carcinoma has been traditionally defined as a tumor of adenohypophysial cells that metastasizes systemically or craniospinally independent of the histological appearance of the lesion. Reported cases of pituitary carcinoma have clinically and histologically resembled their non-metastatic counterparts that were classified as adenomas; the majority of cases were initially diagnosed as adenomas, and with tumor progression and spread, the diagnosis was changed to carcinoma. This classification has been challenged since the definition of malignancy in most organs is not based only on metastatic spread. The extent of local invasion resulting in an inability to completely resect an adenohypophysial tumor can have serious consequences that can cause harm and are therefore not benign. To address this dilemma, it was proposed that pituitary tumors be classified as neuroendocrine tumors. This change in nomenclature is totally appropriate since these tumors are composed of classical neuroendocrine cells; as with other neuroendocrine tumors, they have variable behavior that can be indolent but can involve metastasis. With the new nomenclature, there is no requirement for a distinction between adenomas and carcinomas. Moreover, the WHO/IARC has provided an overarching classification for neuroendocrine neoplasms at all body sites; in this new classification, the term ‘neuroendocrine carcinoma’ is reserved for poorly differentiated high-grade malignancies that are clinically, morphologically and genetically distinct from well-differentiated neuroendocrine tumors. It remains to be determined if there are true pituitary neuroendocrine carcinomas.
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spelling doaj.art-c704222f3fb54f3c8c41018e299d39b92023-01-11T12:10:37ZengBioscientificaEndocrine Oncology2634-47932023-01-0121R14R23https://doi.org/10.1530/EO-22-0041Pituitary carcinoma: reclassification and implications in the NET schemaSylvia L Asa0Shereen Ezzat1Department of Pathology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio, USADepartment of Medicine, University Health Network, University of Toronto, Toronto, Ontario, CanadaThe entity known as pituitary carcinoma has been traditionally defined as a tumor of adenohypophysial cells that metastasizes systemically or craniospinally independent of the histological appearance of the lesion. Reported cases of pituitary carcinoma have clinically and histologically resembled their non-metastatic counterparts that were classified as adenomas; the majority of cases were initially diagnosed as adenomas, and with tumor progression and spread, the diagnosis was changed to carcinoma. This classification has been challenged since the definition of malignancy in most organs is not based only on metastatic spread. The extent of local invasion resulting in an inability to completely resect an adenohypophysial tumor can have serious consequences that can cause harm and are therefore not benign. To address this dilemma, it was proposed that pituitary tumors be classified as neuroendocrine tumors. This change in nomenclature is totally appropriate since these tumors are composed of classical neuroendocrine cells; as with other neuroendocrine tumors, they have variable behavior that can be indolent but can involve metastasis. With the new nomenclature, there is no requirement for a distinction between adenomas and carcinomas. Moreover, the WHO/IARC has provided an overarching classification for neuroendocrine neoplasms at all body sites; in this new classification, the term ‘neuroendocrine carcinoma’ is reserved for poorly differentiated high-grade malignancies that are clinically, morphologically and genetically distinct from well-differentiated neuroendocrine tumors. It remains to be determined if there are true pituitary neuroendocrine carcinomas.https://eo.bioscientifica.com/view/journals/eo/2/1/EO-22-0041.xmlpituitaryadenomaneuroendocrine tumorcarcinomainvasionmetastasis
spellingShingle Sylvia L Asa
Shereen Ezzat
Pituitary carcinoma: reclassification and implications in the NET schema
Endocrine Oncology
pituitary
adenoma
neuroendocrine tumor
carcinoma
invasion
metastasis
title Pituitary carcinoma: reclassification and implications in the NET schema
title_full Pituitary carcinoma: reclassification and implications in the NET schema
title_fullStr Pituitary carcinoma: reclassification and implications in the NET schema
title_full_unstemmed Pituitary carcinoma: reclassification and implications in the NET schema
title_short Pituitary carcinoma: reclassification and implications in the NET schema
title_sort pituitary carcinoma reclassification and implications in the net schema
topic pituitary
adenoma
neuroendocrine tumor
carcinoma
invasion
metastasis
url https://eo.bioscientifica.com/view/journals/eo/2/1/EO-22-0041.xml
work_keys_str_mv AT sylvialasa pituitarycarcinomareclassificationandimplicationsinthenetschema
AT shereenezzat pituitarycarcinomareclassificationandimplicationsinthenetschema