Carcinoid syndrome in patients with neuroendocrine tumors is a challenging condition that requires accurate diagnostic and therapeutic management by a multidisciplinary team. Therefore, this review intends to detail all clinical aspects of carcinoid syndrome in order to provide clinicians with a definite overview of the effective approach to carcinoid syndrome. In this way, the review aims to improve patient care and treatment outcomes in this patient population.

Exploring carcinoid syndrome in neuroendocrine tumors: insights from a multidisciplinary narrative review / Marasco, Matteo; Romano, Elena; Arrivi, Giulia; Prosperi, Daniela; Rinzivillo, Maria; Caruso, Damiano; Mercantini, Paolo; Rossi, Michele; Faggiano, Antongiulio; Panzuto, Francesco. - In: CANCERS. - ISSN 2072-6694. - 16:22(2024). [10.3390/cancers16223831]

Exploring carcinoid syndrome in neuroendocrine tumors: insights from a multidisciplinary narrative review

Marasco, Matteo
Primo
;
Romano, Elena;Arrivi, Giulia;Prosperi, Daniela;Rinzivillo, Maria;Caruso, Damiano;Mercantini, Paolo;Rossi, Michele;Faggiano, Antongiulio;Panzuto, Francesco
Ultimo
2024

Abstract

Carcinoid syndrome in patients with neuroendocrine tumors is a challenging condition that requires accurate diagnostic and therapeutic management by a multidisciplinary team. Therefore, this review intends to detail all clinical aspects of carcinoid syndrome in order to provide clinicians with a definite overview of the effective approach to carcinoid syndrome. In this way, the review aims to improve patient care and treatment outcomes in this patient population.
2024
cancer; carcinoid syndrome; multidisciplinary team; neuroendocrine tumor
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Exploring carcinoid syndrome in neuroendocrine tumors: insights from a multidisciplinary narrative review / Marasco, Matteo; Romano, Elena; Arrivi, Giulia; Prosperi, Daniela; Rinzivillo, Maria; Caruso, Damiano; Mercantini, Paolo; Rossi, Michele; Faggiano, Antongiulio; Panzuto, Francesco. - In: CANCERS. - ISSN 2072-6694. - 16:22(2024). [10.3390/cancers16223831]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1729413
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