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What Are the Place and Modalities of Surgical Management for Pancreatic Neuroendocrine Neoplasms? A Narrative Review
SIMPLE SUMMARY: Although pancreatic neuroendocrine neoplasms represent less than 5% of all pancreatic cancers, their incidence rate has risen dramatically over the last decade, mainly due to improved detection methods. They are considered malignant by default. However, their outcomes are variable de...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656750/ https://www.ncbi.nlm.nih.gov/pubmed/34885063 http://dx.doi.org/10.3390/cancers13235954 |
Sumario: | SIMPLE SUMMARY: Although pancreatic neuroendocrine neoplasms represent less than 5% of all pancreatic cancers, their incidence rate has risen dramatically over the last decade, mainly due to improved detection methods. They are considered malignant by default. However, their outcomes are variable depending on their presentation in the onset of hereditary syndromes, hormonal secretion, grading, and extension. Therefore, although surgical treatment has long been suggested as the only treatment of pancreatic neuroendocrine neoplasms, its modalities are an evolving landscape, especially since parenchyma-sparring pancreatectomy and endoscopic approaches instead of large pancreatic resections have been proposed. Moreover, in selected cases, watchful strategies are on balance with surgical resection, but the accurate size cut-off of the tumor remains to be established. The aim of this narrative review is to describe the current recommended surgical management for pancreatic NENs and controversies in light of the actual recommendations and recent literature. ABSTRACT: Pancreatic neuroendocrine neoplasms (panNENs) are a heterogeneous group of tumors derived from cells with neuroendocrine differentiation. They are considered malignant by default. However, their outcomes are variable depending on their presentation in the onset of hereditary syndromes, hormonal secretion, grading, and extension. Therefore, although surgical treatment has long been suggested as the only treatment of pancreatic neuroendocrine neoplasms, its modalities are an evolving landscape. For selected patients (small, localized, non-functional panNENs), a “wait and see” strategy is suggested, as it is in the setting of multiple neuroendocrine neoplasia type 1, but the accurate size cut-off remains to be established. Parenchyma-sparring pancreatectomy, aiming to limit pancreatic insufficiency, are also emerging procedures, which place beyond the treatment of insulinomas and small non-functional panNENs (in association with lymph node picking) remains to be clarified. Furthermore, giving the fact that the liver is generally the only metastatic site, surgery keeps a place of choice alongside medical therapies in the treatment of metastatic disease, but its modalities and extensions are still a matter of debate. This narrative review aims to describe the current recommended surgical management for pancreatic NENs and controversies in light of the actual recommendations and recent literature. |
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