134 results on '"De Rose, Agostino Maria"'
Search Results
2. Synchronous Presentation of Primary and Colorectal Liver Metastasis: Classic, Reverse, and Combined
- Author
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Giuliante, Felice, Ardito, Francesco, De Rose, Agostino Maria, Vauthey, Jean-Nicolas, editor, Kawaguchi, Yoshikuni, editor, and Adam, René, editor
- Published
- 2022
- Full Text
- View/download PDF
3. Pancreatico-Jejunostomy On Isolated Loop After Pancreatico-Duodenectomy: Is It Worthwhile?
- Author
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Clemente, Gennaro, De Rose, Agostino Maria, Panettieri, Elena, Ardito, Francesco, Murazio, Marino, Nuzzo, Gennaro, and Giuliante, Felice
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- 2022
- Full Text
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4. Evaluation of the economic impact of the robotic approach in major and postero-superior segment liver resections: a multicenter retrospective analysis
- Author
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Ingallinella, Sara, primary, Ardito, Francesco, additional, Ratti, Francesca, additional, Marino, Rebecca, additional, Catena, Marco, additional, De Rose, Agostino Maria, additional, Razionale, Francesco, additional, Rumi, Filippo, additional, Cicchetti, Americo, additional, Giuliante, Felice, additional, and Aldrighetti, Luca, additional
- Published
- 2024
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5. Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles
- Author
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Farshidfar, Farshad, Zheng, Siyuan, Gingras, Marie-Claude, Newton, Yulia, Shih, Juliann, Robertson, A Gordon, Hinoue, Toshinori, Hoadley, Katherine A, Gibb, Ewan A, Roszik, Jason, Covington, Kyle R, Wu, Chia-Chin, Shinbrot, Eve, Stransky, Nicolas, Hegde, Apurva, Yang, Ju Dong, Reznik, Ed, Sadeghi, Sara, Pedamallu, Chandra Sekhar, Ojesina, Akinyemi I, Hess, Julian M, Auman, J Todd, Rhie, Suhn K, Bowlby, Reanne, Borad, Mitesh J, Network, The Cancer Genome Atlas, Akbani, Rehan, Allotey, Loretta K, Ally, Adrian, Alvaro, Domenico, Andersen, Jesper B, Appelbaum, Elizabeth L, Arora, Arshi, Balasundaram, Miruna, Balu, Saianand, Bardeesy, Nabeel, Bathe, Oliver F, Baylin, Stephen B, Beroukhim, Rameen, Berrios, Mario, Bodenheimer, Tom, Boice, Lori, Bootwalla, Moiz S, Bowen, Jay, Bragazzi, Maria Consiglia, Brooks, Denise, Cardinale, Vincenzo, Carlsen, Rebecca, Carpino, Guido, Carvalho, Andre L, Chaiteerakij, Roongruedee, Chandan, Vishal C, Cherniack, Andrew D, Chin, Lynda, Cho, Juok, Choe, Gina, Chuah, Eric, Chudamani, Sudha, Cibulskis, Carrie, Cordes, Matthew G, Crain, Daniel, Curley, Erin, De Rose, Agostino Maria, Defreitas, Timothy, Demchok, John A, Deshpande, Vikram, Dhalla, Noreen, Ding, Li, Evason, Kimberley, Felau, Ina, Ferguson, Martin L, Foo, Wai Chin, Franchitto, Antonio, Frazer, Scott, Fronick, Catrina C, Fulton, Lucinda A, Fulton, Robert S, Gabriel, Stacey B, Gardner, Johanna, Gastier-Foster, Julie M, Gaudio, Eugenio, Gehlenborg, Nils, Genovese, Giannicola, Gerken, Mark, Getz, Gad, Giama, Nasra H, Gibbs, Richard A, Giuliante, Felice, Grazi, Gian Luca, Hayes, D Neil, Hegde, Apurva M, and Heiman, David I
- Subjects
Liver Cancer ,Digestive Diseases ,Liver Disease ,Biotechnology ,Human Genome ,Genetics ,Cancer ,Rare Diseases ,Digestive Diseases - (Gallbladder) ,Adult ,Aged ,Aged ,80 and over ,Bile Duct Neoplasms ,Cholangiocarcinoma ,Chromatin ,DNA Methylation ,DNA-Binding Proteins ,Female ,Gene Expression Regulation ,Neoplastic ,Genomics ,Humans ,Isocitrate Dehydrogenase ,Liver ,Liver Neoplasms ,Male ,Middle Aged ,Mitochondria ,Mutation ,Nuclear Proteins ,Pancreatic Neoplasms ,Promoter Regions ,Genetic ,RNA ,Long Noncoding ,RNA ,Messenger ,Transcription Factors ,Cancer Genome Atlas Network ,ARID1A ,DNA methylation ,IDH ,RNA sequencing ,TCGA ,cholangiocarcinoma ,integrative genomics ,lncRNAs ,multi-omics ,whole exome ,Biochemistry and Cell Biology ,Medical Physiology - Abstract
Cholangiocarcinoma (CCA) is an aggressive malignancy of the bile ducts, with poor prognosis and limited treatment options. Here, we describe the integrated analysis of somatic mutations, RNA expression, copy number, and DNA methylation by The Cancer Genome Atlas of a set of predominantly intrahepatic CCA cases and propose a molecular classification scheme. We identified an IDH mutant-enriched subtype with distinct molecular features including low expression of chromatin modifiers, elevated expression of mitochondrial genes, and increased mitochondrial DNA copy number. Leveraging the multi-platform data, we observed that ARID1A exhibited DNA hypermethylation and decreased expression in the IDH mutant subtype. More broadly, we found that IDH mutations are associated with an expanded histological spectrum of liver tumors with molecular features that stratify with CCA. Our studies reveal insights into the molecular pathogenesis and heterogeneity of cholangiocarcinoma and provide classification information of potential therapeutic significance.
- Published
- 2017
6. The Italian Consensus on minimally invasive simultaneous resections for synchronous liver metastasis and primary colorectal cancer: A Delphi methodology
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Rocca, Aldo, Cipriani, Federica, Belli, Giulio, Berti, Stefano, Boggi, Ugo, Bottino, Vincenzo, Cillo, Umberto, Cescon, Matteo, Cimino, Matteo, Corcione, Francesco, De Carlis, Luciano, Degiuli, Maurizio, De Paolis, Paolo, De Rose, Agostino Maria, D’Ugo, Domenico, Di Benedetto, Fabrizio, Elmore, Ugo, Ercolani, Giorgio, Ettorre, Giuseppe M., Ferrero, Alessandro, Filauro, Marco, Giuliante, Felice, Gruttadauria, Salvatore, Guglielmi, Alfredo, Izzo, Francesco, Jovine, Elio, Laurenzi, Andrea, Marchegiani, Francesco, Marini, Pierluigi, Massani, Marco, Mazzaferro, Vincenzo, Mineccia, Michela, Minni, Francesco, Muratore, Andrea, Nicosia, Simone, Pellicci, Riccardo, Rosati, Riccardo, Russolillo, Nadia, Spinelli, Antonino, Spolverato, Gaya, Torzilli, Guido, Vennarecci, Giovanni, Viganò, Luca, Vincenti, Leonardo, Delrio, Paolo, Calise, Fulvio, and Aldrighetti, Luca
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- 2021
- Full Text
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7. Ovarian cancer metastases in the liver area: proposal of a standardized anatomo-surgical classification
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Rosati, Andrea, De Rose, Agostino Maria, Sala, Evis, Giuliante, Felice, Scambia, Giovanni, and Fagotti, Anna
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- 2022
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8. Prognostic factors value of germline and somatic brca in patients undergoing surgery for recurrent ovarian cancer with liver metastases
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Gallotta, Valerio, Conte, Carmine, D’Indinosante, Marco, Capoluongo, Ettore, Minucci, Angelo, De Rose, Agostino Maria, Ardito, Francesco, Giuliante, Felice, Di Giorgio, Andrea, Zannoni, Gian Franco, Fagotti, Anna, Margreiter, Christian, Scambia, Giovanni, and Ferrandina, Gabriella
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- 2019
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9. Posterior Right Disconnected Bile Duct
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Cillo, Umberto, Boetto, Riccardo, De Rose, Agostino Maria, Bassi, Domenico, Ardito, Francesco, Giuliante, Felice, Pawlik, Timothy M., editor, Weber, Sharon, editor, and Gamblin, T. Clark, editor
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- 2017
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10. Secondary Laparoscopic Cytoreduction in Recurrent Ovarian Cancer: A Large, Single-Institution Experience
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Gallotta, Valerio, Conte, Carmine, Giudice, Maria Teresa, Nero, Camilla, Vizzielli, Giuseppe, Gueli Alletti, Salvatore, Cianci, Stefano, Lodoli, Claudio, Di Giorgio, Andrea, De Rose, Agostino Maria, Fagotti, Anna, Scambia, Giovanni, and Ferrandina, Gabriella
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- 2018
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11. Cystic Bile Duct Dilatations and Caroli’s Disease
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Giuliante, Felice, De Rose, Agostino Maria, Nuzzo, Gennaro, Aldrighetti, Luca, editor, Cetta, Francesco, editor, and Ferla, Gianfranco, editor
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- 2015
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12. Hepatolithiasis
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Giuliante, Felice, De Rose, Agostino Maria, Nuzzo, Gennaro, Aldrighetti, Luca, editor, Cetta, Francesco, editor, and Ferla, Gianfranco, editor
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- 2015
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13. Solitary fibrous tumor of the liver with Doege-Potter syndrome: An exceptional finding. Discovering the role of blood glucose levels and insulin growth factor II
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Taliente, Francesco, primary, De Rose, Agostino Maria, additional, Ardito, Francesco, additional, and Giuliante, Felice, additional
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- 2022
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14. Hepatoceliac Lymph Node Involvement in Advanced Ovarian Cancer Patients: Prognostic Role and Clinical Considerations
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Gallotta, Valerio, Ferrandina, Gabriella, Vizzielli, Giuseppe, Conte, Carmine, Lucidi, Alessandro, Costantini, Barbara, De Rose, Agostino Maria, Di Giorgio, Andrea, Zannoni, Gian Franco, Fagotti, Anna, Scambia, Giovanni, and Chiantera, Vito
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- 2017
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15. 2022-RA-1456-ESGO Ovarian cancer metastases in the liver area: a retrospective analysis of surgical, intraoperative and postoperative outcomes according to a standardize anatomo-surgical classification
- Author
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Rosati, Andrea, primary, Pavone, Matteo, additional, de Palma, Antonella, additional, Conte, Carmine, additional, Ghirardi, Valentina, additional, de Rose, Agostino Maria, additional, Giuliante, Felice, additional, Scambia, Giovanni, additional, and Fagotti, Anna, additional
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- 2022
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16. Solitary fibrous tumor of the liver with Doege-Potter syndrome: An exceptional finding. Discovering the role of blood glucose levels and insulin growth factor II
- Author
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Taliente, Francesco, De Rose, Agostino Maria, Ardito, Francesco, Giuliante, Felice, Taliente F., De Rose A. M., Ardito F. (ORCID:0000-0003-1596-2862), Giuliante F. (ORCID:0000-0001-9517-8220), Taliente, Francesco, De Rose, Agostino Maria, Ardito, Francesco, Giuliante, Felice, Taliente F., De Rose A. M., Ardito F. (ORCID:0000-0003-1596-2862), and Giuliante F. (ORCID:0000-0001-9517-8220)
- Abstract
N/A
- Published
- 2022
17. Artificial intelligence and its role in guiding liver-directed therapy for hepatocellular carcinoma: Is it ready for prime time?
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Panettieri, Elena, primary, Campisi, Andrea, additional, Bianchi, Valentina, additional, Giuliante, Felice, additional, and De Rose, Agostino Maria, additional
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- 2022
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18. The Mucocele of the Gallbladder
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Clemente, Gennaro, Fico, Valeria, De Sio, Davide, and De Rose, Agostino Maria
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- 2017
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19. Clinical Characteristics and Survival of European Patients with Resectable Large Hepatocellular Carcinomas
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Giuliante, Felice, De Rose, Agostino Maria, Guerra, Vito, Ardito, Francesco, Nuzzo, Gennaro, and Carr, Brian I.
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- 2013
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20. Prognostic Significance of Tumor Doubling Time in Mass-Forming Type Cholangiocarcinoma
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De Rose, Agostino Maria, Cucchetti, Alessandro, Clemente, Gennaro, Ardito, Francesco, Giovannini, Ivo, Ercolani, Giorgio, Giuliante, Felice, Pinna, Antonio Daniele, and Nuzzo, Gennaro
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- 2013
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21. DCLK1, a putative novel stem cell marker in human cholangiocarcinoma
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Safarikia Samira, Monti Marco, Grazi Gian Luca, Caretti Giuseppina, Bosco Daniela, De Peppo Valerio, Invernizzi Pietro, Bragazzi Maria Consiglia, Ambrosino Valeria, Di Matteo Sabina, Zizzari Ilaria Grazia, Overi Diletta, Massironi Sara, Giuliante Felice, Oddi Andrea, Cardinale Vincenzo, Giancotti Antonella, Gaudio Eugenio, Melandro Fabio, Panici P. Benedetti, Berloco Paquale Bartomeo, Carpino Guido, Nevi Lorenzo, Faccioli Jessica, De Rose Agostino Maria, Costantini Daniele, Alvaro Domenico, Nevi, L, Di Matteo, S, Carpino, G, Zizzari, I, Safarikia, S, Ambrosino, V, Costantini, D, Overi, D, Giancotti, A, Monti, M, Bosco, D, De Peppo, V, Oddi, A, De Rose, A, Melandro, F, Bragazzi, M, Faccioli, J, Massironi, S, Grazi, G, Panici, P, Berloco, P, Giuliante, F, Cardinale, V, Invernizzi, P, Caretti, G, Gaudio, E, and Alvaro, D
- Subjects
0301 basic medicine ,Cell ,Cancer Stem Cell ,Protein Serine-Threonine Kinases ,Stem cell marker ,Receptors, G-Protein-Coupled ,NO ,Cholangiocarcinoma ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Doublecortin-Like Kinases ,Cancer stem cell ,Cell Line, Tumor ,Cancer Stem Cells ,medicine ,Biomarkers, Tumor ,Hepatobiliary Malignancies ,Humans ,LS4_6 ,Cell Proliferation ,Invasivene ,Biomarker ,DCAMKL1 ,Invasiveness ,Primary liver cancer ,Hepatology ,Cluster of differentiation ,Chemistry ,Cell growth ,LGR5 ,Intracellular Signaling Peptides and Proteins ,Epithelial cell adhesion molecule ,Original Articles ,Molecular biology ,Gene Expression Regulation, Neoplastic ,030104 developmental biology ,medicine.anatomical_structure ,Bile Duct Neoplasms ,Cell culture ,Neoplastic Stem Cells ,Original Article ,030211 gastroenterology & hepatology ,Erratum - Abstract
Background and aims Cholangiocarcinoma (CCA) is a very aggressive cancer showing the presence of high cancer stem cells (CSCs). Doublecortin-like kinase1 (DCLK1) has been demonstrated as a CSC marker in different gastroenterological solid tumors. Our aim was to evaluate in vitro the expression and the biological function of DCLK1 in intrahepatic CCA (iCCA) and perihilar CCA (pCCA). Approach and results Specimens surgically resected of human CCA were enzymatically digested, submitted to immunosorting for specific CSC markers (LGR5 [leucine-rich repeat-containing G protein-coupled receptor], CD [clusters of differentiation] 90, EpCAM [epithelial cell adhesion molecule], CD133, and CD13), and primary cell cultures were prepared. DCLK1 expression was analyzed in CCA cell cultures by real-time quantitative PCR, western blot, and immunofluorescence. Functional studies have been performed by evaluating the effects of selective DCLK1 inhibitor (LRRK2-IN-1) on cell proliferation (MTS [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium] assay, cell population doubling time), apoptosis, and colony formation capacity. DCLK1 was investigated in situ by immunohistochemistry and real-time quantitative PCR. DCLK1 serum concentration was analyzed by enzyme-linked immunosorbent assay. We describe DCLK1 in CCA with an increased gene and protein DCLK1 expression in pCCALGR5+ and in iCCACD133+ cells compared with unsorted cells. LRRK2-IN-1 showed an anti-proliferative effect in a dose-dependent manner. LRRK2-IN-1 markedly impaired cell proliferation, induced apoptosis, and decreased colony formation capacity and colony size in both iCCA and pCCA compared with the untreated cells. In situ analysis confirmed that DCLK1 is present only in tumors, and not in healthy tissue. Interestingly, DCLK1 was detected in the human serum samples of patients with iCCA (high), pCCA (high), HCC (low), and cirrhosis (low), but it was almost undetectable in healthy controls. Conclusions DCLK1 characterizes a specific CSC subpopulation of iCCACD133+ and pCCALGR5+ , and its inhibition exerts anti-neoplastic effects in primary CCA cell cultures. Human DCLK1 serum might represent a serum biomarker for the early CCA diagnosis.
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- 2021
22. ASO Author Reflections: The Liver-First Approach: A New Standard for Patients with Multiple Bilobar Colorectal Metastases?
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Giuliante, Felice, Vigano, L., De Rose, Agostino Maria, Adam, R., Giuliante F. (ORCID:0000-0001-9517-8220), De Rose A. M., Giuliante, Felice, Vigano, L., De Rose, Agostino Maria, Adam, R., Giuliante F. (ORCID:0000-0001-9517-8220), and De Rose A. M.
- Abstract
The best surgical strategy for patients with colorectal cancer and synchronous liver metastases is a matter of endless debate. Technical and oncological issues must be considered but have often been confounded. In 2006, Mentha et al.1 proposed an innovative and convincing oncosurgical approach, whereby they reversed the strategy, focusing attention on the prognostically most relevant target, i.e. the liver. Even if appealing, the liver-first approach struggled to find its role and failed to demonstrate a benefit, except for the inclusion of chemoradiotherapy in the treatment schedule of patients with locally advanced rectal tumors. The proposers themselves reported non-inferiority (and not superiority) of the reverse strategy in comparison with the standard primary-first approach.2 A recent network meta-analysis ranked the liver-first approach as the best treatment option for its relative efficacy based on 5-year overall survival outcomes,3 but the evidence is too weak to impact current clinical practice.
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- 2021
23. DCLK1, a putative novel stem cell marker in human cholangiocarcinoma
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Nevi, L, Di Matteo, S, Carpino, G, Zizzari, I, Safarikia, S, Ambrosino, V, Costantini, D, Overi, D, Giancotti, A, Monti, M, Bosco, D, De Peppo, V, Oddi, A, De Rose, A, Melandro, F, Bragazzi, M, Faccioli, J, Massironi, S, Grazi, G, Panici, P, Berloco, P, Giuliante, F, Cardinale, V, Invernizzi, P, Caretti, G, Gaudio, E, Alvaro, D, Nevi, Lorenzo, Di Matteo, Sabina, Carpino, Guido, Zizzari, Ilaria, Safarikia, Samira, Ambrosino, Valeria, Costantini, Daniele, Overi, Diletta, Giancotti, Antonella, Monti, Marco, Bosco, Daniela, De Peppo, Valerio, Oddi, Andrea, De Rose, Agostino Maria, Melandro, Fabio, Bragazzi, Maria Consiglia, Faccioli, Jessica, Massironi, Sara, Grazi, Gian Luca, Panici, Pierluigi Benedetti, Berloco, Paquale Bartomeo, Giuliante, Felice, Cardinale, Vincenzo, Invernizzi, Pietro, Caretti, Giuseppina, Gaudio, Eugenio, Alvaro, Domenico, Nevi, L, Di Matteo, S, Carpino, G, Zizzari, I, Safarikia, S, Ambrosino, V, Costantini, D, Overi, D, Giancotti, A, Monti, M, Bosco, D, De Peppo, V, Oddi, A, De Rose, A, Melandro, F, Bragazzi, M, Faccioli, J, Massironi, S, Grazi, G, Panici, P, Berloco, P, Giuliante, F, Cardinale, V, Invernizzi, P, Caretti, G, Gaudio, E, Alvaro, D, Nevi, Lorenzo, Di Matteo, Sabina, Carpino, Guido, Zizzari, Ilaria, Safarikia, Samira, Ambrosino, Valeria, Costantini, Daniele, Overi, Diletta, Giancotti, Antonella, Monti, Marco, Bosco, Daniela, De Peppo, Valerio, Oddi, Andrea, De Rose, Agostino Maria, Melandro, Fabio, Bragazzi, Maria Consiglia, Faccioli, Jessica, Massironi, Sara, Grazi, Gian Luca, Panici, Pierluigi Benedetti, Berloco, Paquale Bartomeo, Giuliante, Felice, Cardinale, Vincenzo, Invernizzi, Pietro, Caretti, Giuseppina, Gaudio, Eugenio, and Alvaro, Domenico
- Abstract
Background & aims: Cholangiocarcinoma (CCA) is a very aggressive cancer showing high cancer stem cells (CSCs) presence. Doublecortin-like kinase1 (DCLK1) has been demonstrated as a CSC marker in different gastroenterological solid tumours. Our aim was to evaluate in vitro the expression and the biological function of DCLK1 in intrahepatic CCA (iCCA) and perihilar CCA (pCCA). Approach & results: Specimens surgically resected of human CCA were enzymatically digested, submitted to immunosorting for specific CSC markers (LGR5, CD90, EpCAM, CD133, CD13) and primary cell cultures were prepared. DCLK1 expression was analysed in CCA cell cultures by real-time quantitative polymerase chain reaction (RT-qPCR), Western Blot and immunofluorescence. Functional studies have been performed by evaluating the effects of selective DCLK1 inhibitor (LRRK2-IN-1) on cell proliferation (MTS-Assay, cell population doubling time), apoptosis and colony formation capacity. DCLK1 was investigated in situ by immunohistochemistry and RT-qPCR. DCLK1 serum concentration was analysed by enzyme-linked immunosorbent assay (ELISA). We describe DCLK1 in CCA with an increased gene and protein DCLK1 expression in pCCALGR5+ and in iCCACD133+ cells compared to unsorted cells. LRRK2-IN-1 showed an anti-proliferative effect in dose-dependent manner. LRRK2-IN-1 markedly impaired cell proliferation, induced apoptosis, decreased colony formation capacity and colony size in both iCCA and pCCA compared to untreated cells. In situ analysis confirm that DCLK1 is present only in tumours, but not in healthy tissue. Interestingly, DCLK1 was detected in the human serum samples of iCCA (high), pCCA (high), HCC (low) and cirrhotic (low) patients, but it was almost undetectable in healthy controls. Conclusion: DCLK1 characterizes a specific CSC-subpopulation of iCCACD133+ and pCCALGR5+ and its inhibition exerts anti-neoplastic effects in primary CCA cell cultures. Human DCLK1 serum might represent a serum biomarke
- Published
- 2021
24. Unexpected Gallbladder Cancer after Laparoscopic Cholecystectomy for Acute Cholecystitis: A Worrisome Picture
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Clemente, Gennaro, Nuzzo, Gennaro, De Rose, Agostino Maria, Giovannini, Ivo, La Torre, Giuseppe, Ardito, Francesco, and Giuliante, Felice
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- 2012
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25. Intrahepatic cholangiocarcinoma: prognostic factors after liver resection
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Nuzzo, Gennaro, Giuliante, Felice, Ardito, Francesco, De Rose, Agostino Maria, Vellone, Maria, Clemente, Gennaro, Chiarla, Carlo, and Giovannini, Ivo
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- 2010
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26. DCLK1, a Putative Stem Cell Marker in Human Cholangiocarcinoma
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Nevi, Lorenzo, primary, Di Matteo, Sabina, additional, Carpino, Guido, additional, Zizzari, Ilaria Grazia, additional, Safarikia, Samira, additional, Ambrosino, Valeria, additional, Costantini, Daniele, additional, Overi, Diletta, additional, Giancotti, Antonella, additional, Monti, Marco, additional, Bosco, Daniela, additional, De Peppo, Valerio, additional, Oddi, Andrea, additional, De Rose, Agostino Maria, additional, Melandro, Fabio, additional, Bragazzi, Maria Consiglia, additional, Faccioli, Jessica, additional, Massironi, Sara, additional, Grazi, Gian Luca, additional, Benedetti Panici, Pierluigi, additional, Berloco, Paquale Bartomeo, additional, Giuliante, Felice, additional, Cardinale, Vincenzo, additional, Invernizzi, Pietro, additional, Caretti, Giuseppina, additional, Gaudio, Eugenio, additional, and Alvaro, Domenico, additional
- Published
- 2021
- Full Text
- View/download PDF
27. Erratum: Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles (Cell Reports (2017) 18(11) (2780â2794) (S2211124717302140) (10.1016/j.celrep.2017.02.033))
- Author
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Farshidfar, Farshad, Zheng, Siyuan, Gingras, Marie-Claude, Newton, Yulia, Shih, Juliann, Robertson, A. Gordon, Hinoue, Toshinori, Hoadley, Katherine A., Gibb, Ewan A., Roszik, Jason, Covington, Kyle R., Wu, Chia-Chin, Shinbrot, Eve, Stransky, Nicolas, Hegde, Apurva, Yang, Ju Dong, Reznik, Ed, Sadeghi, Sara, Pedamallu, Chandra Sekhar, Ojesina, Akinyemi I., Hess, Julian M., Auman, J. Todd, Rhie, Suhn K., Bowlby, Reanne, Borad, Mitesh J., Akbani, Rehan, Allotey, Loretta K., Ally, Adrian, Alvaro, Domenico, Andersen, Jesper B., Appelbaum, Elizabeth L., Arora, Arshi, Balasundaram, Miruna, Balu, Saianand, Bardeesy, Nabeel, Bathe, Oliver F., Baylin, Stephen B., Beroukhim, Rameen, Berrios, Mario, Bodenheimer, Tom, Boice, Lori, Bootwalla, Moiz S., Bowen, Jay, Bragazzi, Maria Consiglia, Brooks, Denise, Cardinale, Vincenzo, Carlsen, Rebecca, Carpino, Guido, Carvalho, Andre L., Chaiteerakij, Roongruedee, Chandan, Vishal C., Cherniack, Andrew D., Chin, Lynda, Cho, Juok, Choe, Gina, Chuah, Eric, Chudamani, Sudha, Cibulskis, Carrie, Cordes, Matthew G., Crain, Daniel, Curley, Erin, De Rose, Agostino Maria, Defreitas, Timothy, Demchok, John A., Deshpande, Vikram, Dhalla, Noreen, Ding, Li, Evason, Kimberley, Felau, Ina, Ferguson, Martin L., Foo, Wai Chin, Franchitto, Antonio, Frazer, Scott, Fronick, Catrina C., Fulton, Lucinda A., Fulton, Robert S., Gabriel, Stacey B., Gardner, Johanna, Gastier-Foster, Julie M., Gaudio, Eugenio, Gehlenborg, Nils, Genovese, Giannicola, Gerken, Mark, Getz, Gad, Giama, Nasra H., Gibbs, Richard A., Giuliante, Felice, Grazi, Gian Luca, Hayes, D. Neil, Hegde, Apurva M., Heiman, David I., Holbrook, Andrea, Holt, Robert A., Hoyle, Alan P., Huang, Mei, Hutter, Carolyn M., Jefferys, Stuart R., Jones, Steven J. M., Jones, Corbin D., Kasaian, Katayoon, Kelley, Robin K., Kim, Jaegil, Kleiner, David E., Kocher, Jean-Pierre A., Kwong, Lawrence N., Lai, Phillip H., Laird, Peter W., Lawrence, Michael S., Leraas, Kristen M., Lichtenberg, Tara M., Lin, Pei, Liu, Wenbin, Liu, Jia, Lolla, Laxmi, Lu, Yiling, Ma, Yussanne, Mallery, David, Mardis, Elaine R., Marra, Marco A., Matsushita, Marcus M., Mayo, Michael, McLellan, Michael D., McRee, Autumn J., Meier, Sam, Meng, Shaowu, Meyerson, Matthew, Mieczkowski, Piotr A., Miller, Christopher A., Mills, Gordon B., Moore, Richard A., Morris, Scott, Mose, Lisle E., Moser, Catherine D., Mounajjed, Taofic, Mungall, Andrew J., Mungall, Karen, Murray, Bradley A., Naresh, Rashi, Noble, Michael S., O'Brien, Daniel R., Parker, Joel S., Patel, Tushar C., Paulauskis, Joseph, Penny, Robert, Perou, Charles M., Perou, Amy H., Pihl, Todd, Radenbaugh, Amie J., Ramirez, Nilsa C., Rathmell, W. Kimryn, Roach, Jeffrey, Roberts, Lewis R., Saksena, Gordon, Sander, Chris, Schein, Jacqueline E., Schmidt, Heather K., Schumacher, Steven E., Shelton, Candace, Shelton, Troy, Shen, Ronglai, Sheth, Margi, Shi, Yan, Shroff, Rachna, Simons, Janae V., Sipahimalani, Payal, Skelly, Tara, Sofia, Heidi J., Soloway, Matthew G., Stoppler, Hubert, Stuart, Josh, Sun, Qiang, Tam, Angela, Tan, Donghui, Tarnuzzer, Roy, Thiessen, Nina, Thorne, Leigh B., Torbenson, Michael S., Van Den Berg, David J., Veluvolu, Umadevi, Verhaak, Roel G. W., Voet, Doug, Wan, Yunhu, Wang, Zhining, Weinstein, John N., Weisenberger, Daniel J., Wheeler, David A., Wilson, Richard K., Wise, Lisa, Wong, Tina, Wu, Ye, Xi, Liu, Yang, Liming, Zenklusen, Jean C., Zhang, Hailei, Zhang, Jiashan (Julia), Zmuda, Erik, Zhu, Andrew X., Stuart, Josh M., Farshidfar, Farshad, Zheng, Siyuan, Gingras, Marie-Claude, Newton, Yulia, Shih, Juliann, Robertson, A. Gordon, Hinoue, Toshinori, Hoadley, Katherine A., Gibb, Ewan A., Roszik, Jason, Covington, Kyle R., Chia-Chin, Wu, Shinbrot, Eve, Stransky, Nicola, Hegde, Apurva, Yang, Ju Dong, Reznik, Ed, Sadeghi, Sara, Pedamallu, Chandra Sekhar, Ojesina, Akinyemi I., Hess, Julian M., Auman, J. Todd, Rhie, Suhn K., Bowlby, Reanne, Borad, Mitesh J., Akbani, Rehan, Allotey, Loretta K., Ally, Adrian, Alvaro, Domenico, Andersen, Jesper B., Appelbaum, Elizabeth L., Arora, Arshi, Balasundaram, Miruna, Balu, Saianand, Bardeesy, Nabeel, Bathe, Oliver F., Baylin, Stephen B., Beroukhim, Rameen, Berrios, Mario, Bodenheimer, Tom, Boice, Lori, Bootwalla, Moiz S., Bowen, Jay, Bragazzi, Maria Consiglia, Brooks, Denise, Cardinale, Vincenzo, Carlsen, Rebecca, Guido, Carpino, Carvalho, Andre L., Chaiteerakij, Roongruedee, Chandan, Vishal C., Cherniack, Andrew D., Chin, Lynda, Cho, Juok, Choe, Gina, Chuah, Eric, Chudamani, Sudha, Cibulskis, Carrie, Cordes, Matthew G., Crain, Daniel, Curley, Erin, De Rose, Agostino Maria, Defreitas, Timothy, Demchok, John A., Deshpande, Vikram, Dhalla, Noreen, Ding, Li, Evason, Kimberley, Felau, Ina, Ferguson, Martin L., Foo, Wai Chin, Franchitto, Antonio, Frazer, Scott, Fronick, Catrina C., Fulton, Lucinda A., Fulton, Robert S., Gabriel, Stacey B., Gardner, Johanna, Gastier-Foster, Julie M., Gaudio, Eugenio, Gehlenborg, Nil, Genovese, Giannicola, Gerken, Mark, Getz, Gad, Giama, Nasra H., Gibbs, Richard A., Giuliante, Felice, Grazi, Gian Luca, Hayes, D. Neil, Hegde, Apurva M., Heiman, David I., Holbrook, Andrea, Holt, Robert A., Hoyle, Alan P., Huang, Mei, Hutter, Carolyn M., Jefferys, Stuart R., Jones, Steven J. M., Jones, Corbin D., Kasaian, Katayoon, Kelley, Robin K., Kim, Jaegil, Kleiner, David E., Kocher, Jean-Pierre A., Kwong, Lawrence N., Lai, Phillip H., Laird, Peter W., Lawrence, Michael S., Leraas, Kristen M., Lichtenberg, Tara M., Lin, Pei, Liu, Wenbin, Liu, Jia, Lolla, Laxmi, Yiling, Lu, Yussanne, Ma, Mallery, David, Mardis, Elaine R., Marra, Marco A., Matsushita, Marcus M., Mayo, Michael, Mclellan, Michael D., Mcree, Autumn J., Meier, Sam, Meng, Shaowu, Meyerson, Matthew, Mieczkowski, Piotr A., Miller, Christopher A., Mills, Gordon B., Moore, Richard A., Morris, Scott, Mose, Lisle E., Moser, Catherine D., Mounajjed, Taofic, Mungall, Andrew J., Mungall, Karen, Murray, Bradley A., Naresh, Rashi, Noble, Michael S., O'Brien, Daniel R., Parker, Joel S., Patel, Tushar C., Paulauskis, Joseph, Penny, Robert, Perou, Charles M., Perou, Amy H., Pihl, Todd, Radenbaugh, Amie J., Ramirez, Nilsa C., Rathmell, W. Kimryn, Roach, Jeffrey, Roberts, Lewis R., Saksena, Gordon, Sander, Chri, Schein, Jacqueline E., Schmidt, Heather K., Schumacher, Steven E., Shelton, Candace, Shelton, Troy, Shen, Ronglai, Sheth, Margi, Shi, Yan, Shroff, Rachna, Simons, Janae V., Sipahimalani, Payal, Skelly, Tara, Sofia, Heidi J., Soloway, Matthew G., Stoppler, Hubert, Stuart, Josh, Sun, Qiang, Tam, Angela, Tan, Donghui, Tarnuzzer, Roy, Thiessen, Nina, Thorne, Leigh B., Torbenson, Michael S., Van Den Berg, David J., Veluvolu, Umadevi, Verhaak, Roel G. W., Voet, Doug, Wan, Yunhu, Wang, Zhining, Weinstein, John N., Weisenberger, Daniel J., Wheeler, David A., Wilson, Richard K., Wise, Lisa, Wong, Tina, Ye, Wu, Liu, Xi, Yang, Liming, Zenklusen, Jean C., Zhang, Hailei, Zhang, Jiashan (Julia), Zmuda, Erik, Zhu, Andrew X., and Stuart, Josh M.
- Subjects
Genetics and Molecular Biology (all) ,Biochemistry, Genetics and Molecular Biology (all) ,Biochemistry - Abstract
Cholangiocarcinoma (CCA) is an aggressive malignancy of the bile ducts, with poor prognosis and limited treatment options. Here, we describe the integrated analysis of somatic mutations, RNA expression, copy number, and DNA methylation by The Cancer Genome Atlas of a set of predominantly intrahepatic CCA cases and propose a molecular classification scheme. We identified an IDH mutant-enriched subtype with distinct molecular features including low expression of chromatin modifiers, elevated expression of mitochondrial genes, and increased mitochondrial DNA copy number. Leveraging the multi-platform data, we observed that ARID1A exhibited DNA hypermethylation and decreased expression in the IDH mutant subtype. More broadly, we found that IDH mutations are associated with an expanded histological spectrum of liver tumors with molecular features that stratify with CCA. Our studies reveal insights into the molecular pathogenesis and heterogeneity of cholangiocarcinoma and provide classification information of potential therapeutic significance.
- Published
- 2017
28. Poster Session 4: Acute Liver Failure and Artificial Liver Support; Diagnostics, Epidemiology, and Natural History
- Author
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Antonio Gasbarrini, Francesco Russo, Liliana Chemello, Teresa Santantonio, Luchino Chessa, Paolo Caraceni, M. Puoti, Al Zignego, M. Rizzetto, Marco Marzioni, A. Di Leo, Carlo Ferrari, P. Andreone, Stefano Rosato, Pierluigi Blanc, A. Kondili L A Loreta, Me Tosti, Maurizia Rossana Brunetto, L. E. Weimer, G. Raimondo, Michele Quaranta, Raffaele Bruno, Carmine Coppola, Alessandra Mallano, Loredana Falzano, Gabriella Verucchi, Alfredo Alberti, G. Taliani, E.M. Erne, M Massella, Maria Cristina Vinci, Erica Villa, Marcello Persico, Stefano Vella, Giovanna Fattovich, De Rose Agostino Maria, G.B. Gaeta, M. Andreoni, Guglielmo Borgia, and Antonio Craxì
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Prioritization ,Pediatrics ,medicine.medical_specialty ,Life evaluation ,Hepatology ,CpG site ,business.industry ,Cohort ,Medicine ,business ,Studio - Published
- 2015
29. Mirizzi Syndrome: Diagnosis and Management of a Challenging Biliary Disease
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Clemente, Gennaro, Tringali, Andrea, De Rose, Agostino Maria, Panettieri, Elena, Murazio, Marino, Nuzzo, Gennaro, Giuliante, Felice, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Tringali, Andrea (ORCID:0000-0002-9614-3449), De Rose, Agostino M., Murazio, Marino (ORCID:0000-0003-4863-0434), Giuliante, Felice (ORCID:0000-0001-9517-8220), Clemente, Gennaro, Tringali, Andrea, De Rose, Agostino Maria, Panettieri, Elena, Murazio, Marino, Nuzzo, Gennaro, Giuliante, Felice, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Tringali, Andrea (ORCID:0000-0002-9614-3449), De Rose, Agostino M., Murazio, Marino (ORCID:0000-0003-4863-0434), and Giuliante, Felice (ORCID:0000-0001-9517-8220)
- Abstract
Background. Mirizzi syndrome is a condition difficult to diagnose and treat, representing a particular "challenge" for the biliary surgeon. The disease can mimic cancer of the gallbladder, causing considerable diagnostic difficulties. Furthermore, it increases the risk of intraoperative biliary injury during cholecystectomy. The aim of this study is to point out some particular aspects of diagnosis and treatment of this condition. Methods. The clinical records of patients with Mirizzi syndrome, treated in the last five years, were reviewed. Clinical data, cholangiograms, preoperative diagnosis, operative procedures, and early and late results were examined. Results. Eighteen consecutive patients were treated in the last five years. Presenting symptoms were jaundice, pain, and cholangitis. Preoperative diagnosis of Mirizzi syndrome was achieved in 11 patients, while 6 had a diagnosis of gallbladder cancer and 1 of Klatskin tumor. Seventeen patients underwent surgery, including cholecystectomy in 8 cases, bile duct repair over T-tube in 3 cases, and hepaticojejunostomy in 4 cases. Two cases (11.1%) of gallbladder cancer associated with the Mirizzi syndrome were incidentally found: a patient underwent right hepatectomy and another patient was unresectable. The overall morbidity rate was 16.6%. There was no postoperative mortality. An ERCP with stent insertion was required in three cases after surgery. Sixteen patients were asymptomatic at a mean distance of 24 months (range: 6-48) after surgery. Conclusions. Mirizzi syndrome requires being treated by an experienced biliary surgeon after a careful assessment of the local situation and anatomy. The preoperative placement of a stent via ERCP can simplify the surgical procedure.
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- 2018
30. Secondary Laparoscopic Cytoreduction in Recurrent Ovarian Cancer: A Large, Single-Institution Experience
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Gallotta, Valerio, Conte, Carmine, Giudice, Maria Teresa, Nero, Camilla, Vizzielli, Giuseppe, Gueli Alletti, Salvatore, Cianci, Stefano, Lodoli, Claudio, Di Giorgio, Andrea, De Rose, Agostino Maria, Fagotti, Anna, Scambia, Giovanni, Ferrandina, Maria Gabriella, Fagotti, Anna (ORCID:0000-0001-5579-335X), Scambia, Giovanni (ORCID:0000-0003-2758-1063), Ferrandina, Gabriella (ORCID:0000-0003-4672-4197), Gallotta, Valerio, Conte, Carmine, Giudice, Maria Teresa, Nero, Camilla, Vizzielli, Giuseppe, Gueli Alletti, Salvatore, Cianci, Stefano, Lodoli, Claudio, Di Giorgio, Andrea, De Rose, Agostino Maria, Fagotti, Anna, Scambia, Giovanni, Ferrandina, Maria Gabriella, Fagotti, Anna (ORCID:0000-0001-5579-335X), Scambia, Giovanni (ORCID:0000-0003-2758-1063), and Ferrandina, Gabriella (ORCID:0000-0003-4672-4197)
- Abstract
Study Objective: To analyze the feasibility and safety of laparoscopic secondary cytoreductive surgery in a retrospective series of patients with platinum-sensitive recurrent ovarian cancer. Design: Retrospective cohort study (Canadian Task Force classification II-2). Setting: Catholic University of the Sacred Heart, Rome, Italy. Patients: Between October 2010 and October 2016, 58 patients with recurrent ovarian cancer were selected for a retrospective analysis of data. Interventions: All patients underwent a laparoscopic secondary cytoreduction with single or multiple procedures. Results: The most frequent pattern of recurrence was peritoneal (48.3%); 6 patients (10.3%) experienced parenchymal disease (spleen, n = 5; liver, n = 1), and 24 patients (41.4%) had lymph node recurrence. Complete debulking was achieved in all patients. The median operative time was 204 minutes (range, 55-448 minutes), median estimated blood loss was 70 mL (range, 20-300 mL), and the median length of hospital stay was 4 days (range, 1-21 days). Four patients (6.8%) experienced intraoperative complications. Early postoperative complications were documented in 6 patients (10.3%), but only 1 G3 complication was noted. The median duration of follow-up since secondary cytoreduction was 24 months (range, 9-71 months). Twenty-one patients (36.2%) experienced a second disease relapse. The median progression-free survival (PFS) was 28 months, and the 2-year PFS was 58.7%. Five patients died (8.6%); the 2-year overall survival was 90.7%. Conclusions: For selected patients, laparoscopy is a feasible and safe approach to optimal cytoreduction for patients with recurrent ovarian cancer.
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- 2017
31. A Novel Nomogram to Predict the Prognosis of Patients Undergoing Liver Resection for Neuroendocrine Liver Metastasis: an Analysis of the Italian Neuroendocrine Liver Metastasis Database
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Ruzzenente, Andrea, Bagante, Fabio, Bertuzzo, Francesca, Aldrighetti, Luca, Ercolani, Giorgio, Giuliante, Felice, Ferrero, Alessandro, Torzilli, Guido, Grazi, Gian Luca, Ratti, Francesca, Cucchetti, Alessandro, De Rose, Agostino Maria, Russolillo, Nadia, Cimino, Matteo, Perri, Pasquale, Cataldo, Ivana, Scarpa, Aldo, Guglielmi, Alfredo, Iacono, Calogero, Giuliante, Felice (ORCID:0000-0001-9517-8220), Ruzzenente, Andrea, Bagante, Fabio, Bertuzzo, Francesca, Aldrighetti, Luca, Ercolani, Giorgio, Giuliante, Felice, Ferrero, Alessandro, Torzilli, Guido, Grazi, Gian Luca, Ratti, Francesca, Cucchetti, Alessandro, De Rose, Agostino Maria, Russolillo, Nadia, Cimino, Matteo, Perri, Pasquale, Cataldo, Ivana, Scarpa, Aldo, Guglielmi, Alfredo, Iacono, Calogero, and Giuliante, Felice (ORCID:0000-0001-9517-8220)
- Abstract
Even though surgery remains the only potentially curative option for patients with neuroendocrine liver metastases, the factors determining a patient’s prognosis following hepatectomy are poorly understood. Using a multicentric database including patients who underwent hepatectomy for NELMs at seven tertiary referral hepato-biliary-pancreatic centers between January 1990 and December 2014, we sought to identify the predictors of survival and develop a clinical tool to predict patient’s prognosis after liver resection for NELMs. The median age of the 238 patients included in the study was 61.9 years (interquartile range 51.5–70.1) and 55.9 % (n = 133) of patients were men. The number of NELMs (hazard ratio = 1.05), tumor size (HR = 1.01), and Ki-67 index (HR = 1.07) were the predictors of overall survival. These variables were used to develop a nomogram able to predict survival. According to the predicted 5-year OS, patients were divided into three different risk classes: 19.3, 55.5, and 25.2 % of patients were in low (>80 % predicted 5-year OS), medium (40–80 % predicted 5-year OS), and high (<40 % predicted 5-year OS) risk classes. The 10-year OS was 97.0, 55.9, and 20.0 % in the low, medium, and high-risk classes, respectively (p < 0.001). We developed a novel nomogram that accurately (c-index >70 %) staged and predicted the prognosis of patients undergoing liver resection for NELMs.
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- 2017
32. Association of lymph node status with survival in patients after liver resection for hilar cholangiocarcinoma in an Italian multicenter analysis
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Giuliante, Felice, Ardito, Francesco, Guglielmi, Alfredo, Aldrighetti, Luca, Ferrero, Alessandro, Calise, Fulvio, Giulini, Stefano M., Jovine, Elio, Breccia, Claudio, De Rose, Agostino Maria, Pinna, Antonio D., Nuzzo, Gennaro, Giuliante, Felice (ORCID:0000-0001-9517-8220), Ardito, Francesco (ORCID:0000-0003-1596-2862), Giuliante, Felice, Ardito, Francesco, Guglielmi, Alfredo, Aldrighetti, Luca, Ferrero, Alessandro, Calise, Fulvio, Giulini, Stefano M., Jovine, Elio, Breccia, Claudio, De Rose, Agostino Maria, Pinna, Antonio D., Nuzzo, Gennaro, Giuliante, Felice (ORCID:0000-0001-9517-8220), and Ardito, Francesco (ORCID:0000-0003-1596-2862)
- Abstract
Importance: The prognostic value of lymph node (LN) assessment after liver resection for hilar cholangiocarcinoma (HC) is still controversial, and the number of LNs required to be removed to obtain adequate staging is not well defined. Objectives: To evaluate the LN status in patients after liver resection for HC and to clarify which prognostic factor (the number of positive LNs or the LN ratio [LNR]) was most accurate for staging and what minimum number of retrieved LNs was required for adequate staging. Design, Setting, and Participants: Retrospective multicenter study of patients who underwent resection for HC between January 1, 1992, and December 31, 2007, at 8 hepatobiliary Italian centers. The last follow-up was assessed in July 2014. Main Outcome and Measures: Differences in overall survival (OS) according to the LN status were analyzed. The OS results were defined as actual because all included patients completed a 5-year follow-up. Results: One-hundred seventy-five patients with 1133 retrieved LNs were analyzed. The mean (SD) age of the cohort was 63 (10) years, and 42.9%(75 of 175) were female. The median number of LNs examined per patient was 6.5. Forty percent (70 of 175) had LN metastasis. An LNR exceeding 0.20 was associated with significantly lower 5-year OS than an LNR of 0.20 or less (10.6%vs 24.4%; odds ratio, 2.434; 95%CI, 1.020-5.810; P = .04). On multivariable analysis, the LNR was the only independent prognostic factor for OS but was influenced by the total number of retrieved LNs. The LNR was greater than 0.20 in all patients (30 of 30) with 1 to 4 retrieved LNs and in 52.5%(21 of 40) of patients with at least 5 retrieved LNs. Five-year OS in patients with 1 to 5 retrieved LNs was significantly lower than that in those with 6 to 7 retrieved LNs and those with at least 8 retrieved LNs (34.2%, 64.5%, and 62.7%, respectively; P = .047). Five-year OS did not significantly improve when the number of retrieved LNs was greater than 6. These results w
- Published
- 2016
33. Liver resection for primary intrahepatic stones: Focus on postoperative infectious complications
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Clemente, Gennaro, De Rose, Agostino Maria, Murri, Rita, Ardito, Francesco, Nuzzo, Gennaro, Giuliante, Felice, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Murri, Rita (ORCID:0000-0003-4263-7854), Ardito, Francesco (ORCID:0000-0003-1596-2862), Giuliante, Felice (ORCID:0000-0001-9517-8220), Clemente, Gennaro, De Rose, Agostino Maria, Murri, Rita, Ardito, Francesco, Nuzzo, Gennaro, Giuliante, Felice, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Murri, Rita (ORCID:0000-0003-4263-7854), Ardito, Francesco (ORCID:0000-0003-1596-2862), and Giuliante, Felice (ORCID:0000-0001-9517-8220)
- Abstract
Background Primary intrahepatic lithiasis is defined by the presence of gallstones at the level of cystic dilatations of the intrahepatic biliary tree. Liver resection is considered the treatment of choice, with the purpose of removing stones and atrophic parenchyma, also reducing the risk of cholangiocarcinoma. However, in consequence of the considerable incidence of infectious complications, postoperative morbidity remains high. The current study was designed to evaluate the impact of preoperative bacterial colonization of the bile ducts on postoperative outcome. Methods The clinical records of 73 patients treated with liver resection were reviewed and clinical data, operative procedures, results of bile cultures, and postoperative outcomes were examined. Results Left hepatectomy (38 patients) and left lateral sectionectomy (19 patients) were the most frequently performed procedures. Overall morbidity was 38.3 %. A total of 133 microorganisms were isolated from bile. Multivariate analysis identified previous endoscopic or percutaneous cholangiography (p = 0.043) and preoperative cholangitis (p = 0.003) as the only two independent risk factors for postoperative infectious complications. Conclusions Postoperative morbidity was strictly related to the preoperative biliary infection. An effective control of infections should be always pursued before liver resection for intrahepatic stones and an aggressive treatment of early signs of sepsis should be strongly emphasized.
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- 2016
34. Metabolic consequences of the occlusion of the main pancreatic duct with acrylic glue after pancreaticoduodenectomy
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MEZZA, TERESA, CLEMENTE, GENNARO, SORICE, GIANPIO, CONTE, CATERINA, DE ROSE, AGOSTINO MARIA, SUN, VINSIN ALICE, CEFALO, CHIARA MARIA ASSUNTA, PONTECORVI, ALFREDO, NUZZO, GENNARO, GIACCARI, ANDREA, MEZZA, TERESA, CLEMENTE, GENNARO, SORICE, GIANPIO, CONTE, CATERINA, DE ROSE, AGOSTINO MARIA, SUN, VINSIN ALICE, CEFALO, CHIARA MARIA ASSUNTA, PONTECORVI, ALFREDO, NUZZO, GENNARO, and GIACCARI, ANDREA
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- 2015
35. Sensitivity of human intrahepatic cholangiocarcinoma subtypes to chemotherapeutics and molecular targeted agents: A study on primary cell cultures
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Fraveto, Alice, Cardinale, Vincenzo, Bragazzi, Maria Consiglia, Giuliante, Felice, De Rose, Agostino Maria, Grazi, Gian Luca, Napoletano, Chiara, Semeraro, Rossella, Lustri, Anna Maria, Costantini, Daniele, Nevi, Lorenzo, Di Matteo, Sabina, Renzi, Anastasia, Carpino, Guido, Gaudio, Eugenio, Alvaro, Domenico, Giuliante, Felice (ORCID:0000-0001-9517-8220), Fraveto, Alice, Cardinale, Vincenzo, Bragazzi, Maria Consiglia, Giuliante, Felice, De Rose, Agostino Maria, Grazi, Gian Luca, Napoletano, Chiara, Semeraro, Rossella, Lustri, Anna Maria, Costantini, Daniele, Nevi, Lorenzo, Di Matteo, Sabina, Renzi, Anastasia, Carpino, Guido, Gaudio, Eugenio, Alvaro, Domenico, and Giuliante, Felice (ORCID:0000-0001-9517-8220)
- Abstract
We investigated the sensitivity of intrahepatic cholangiocarcinoma (IHCCA) subtypes to chemotherapeutics and molecular targeted agents. Primary cultures of mucin-and mixed-IHCCA were prepared from surgical specimens (N. 18 IHCCA patients) and evaluated for cell proliferation (MTS assay) and apoptosis (Caspase 3) after incubation (72 hours) with increasing concentrations of different drugs. In vivo, subcutaneous human tumor xenografts were evaluated. Primary cultures of mucin-and mixed-IHCCA were characterized by a different pattern of expression of cancer stem cell markers, and by a different drug sensitivity. Gemcitabine and the Gemcitabine-Cisplatin combination were more active in inhibiting cell proliferation in mixed-IHCCA while Cisplatin or Abraxane were more effective against mucin-IHCCA, where Abraxane also enhances apoptosis. 5-Fluoracil showed a slight inhibitory effect on cell proliferation that was more significant in mixed-than mucin-IHCCA primary cultures and, induced apoptosis only in mucin-IHCCA. Among Hg inhibitors, LY2940680 and Vismodegib showed slight effects on proliferation of both IHCCA subtypes. The tyrosine kinase inhibitors, Imatinib Mesylate and Sorafenib showed significant inhibitory effects on proliferation of both mucin-and mixed-IHCCA. The MEK 1/2 inhibitor, Selumetinib, inhibited proliferation of only mucin-IHCCA while the aminopeptidase-N inhibitor, Bestatin was more active against mixed-IHCCA. The c-erbB2 blocking antibody was more active against mixed-IHCCA while, the Wnt inhibitor, LGK974, similarly inhibited proliferation of mucin-and mixed-IHCCA. Either mucin-or mixed-IHCCA showed high sensitivity to nanomolar concentrations of the dual PI3-kinase/mTOR inhibitor, NVP-BEZ235. In vivo, in subcutaneous xenografts, either NVP-BEZ235 or Abraxane, blocked tumor growth. In conclusion, mucin-and mixed-IHCCA are characterized by a different drug sensitivity. Cisplatin, Abraxane and the MEK 1/2 inhibitor, Selumetinib were more active again
- Published
- 2015
36. Enhancement patterns of intrahepatic mass-forming cholangiocarcinoma at multiphasic computed tomography and magnetic resonance imaging and correlation with clinicopathologic features
- Author
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Ciresa, Marzia, De Gaetano, Anna Maria, Pompili, Maurizio, Saviano, Antonio, Infante, Amato, Montagna, Marco, Guerra, Alessandra, Giuga, Maria, Vellone, Maria, Ardito, Francesco, De Rose, Agostino Maria, Giuliante, Felice, Vecchio, F. M, Gasbarrini, Antonio, Bonomo, Lorenzo, De Gaetano, Anna Maria (ORCID:0000-0002-7493-9462), Pompili, Maurizio (ORCID:0000-0001-6699-7980), Vellone, Maria (ORCID:0000-0002-7628-4092), Ardito, Francesco (ORCID:0000-0003-1596-2862), Giuliante, Felice (ORCID:0000-0001-9517-8220), Gasbarrini, Antonio (ORCID:0000-0002-7278-4823), Bonomo, Lorenzo (ORCID:0000-0001-5101-9367), Ciresa, Marzia, De Gaetano, Anna Maria, Pompili, Maurizio, Saviano, Antonio, Infante, Amato, Montagna, Marco, Guerra, Alessandra, Giuga, Maria, Vellone, Maria, Ardito, Francesco, De Rose, Agostino Maria, Giuliante, Felice, Vecchio, F. M, Gasbarrini, Antonio, Bonomo, Lorenzo, De Gaetano, Anna Maria (ORCID:0000-0002-7493-9462), Pompili, Maurizio (ORCID:0000-0001-6699-7980), Vellone, Maria (ORCID:0000-0002-7628-4092), Ardito, Francesco (ORCID:0000-0003-1596-2862), Giuliante, Felice (ORCID:0000-0001-9517-8220), Gasbarrini, Antonio (ORCID:0000-0002-7278-4823), and Bonomo, Lorenzo (ORCID:0000-0001-5101-9367)
- Abstract
OBJECTIVE: Incidence of intrahepatic mass-forming cholangiocarcinoma (IMCC) is increasing worldwide, especially in patients with chronic liver disease. The small and the histologically well-differentiated IMCCs in chronic liver disease could be arterially hypervascular lesions with/without washout on computed tomography (CT) and magnetic resonance imaging (MRI), mimicking typical hepatocellular carcinoma (HCC). The aim of this work is to evaluate contrast enhancement (CE) patterns of IMCCs at quadri-phasic multidetector CT (4-MDCT) and MRI, using imaging-clinicopathologic correlation. PATIENTS AND METHODS: The 4-MDCT and MR images of 56 histologically confirmed IMCCs were retrospectively evaluated for tumor morphology and enhancement features. Enhancement pattern was defined according to the behavior of the nodule in arterial (AP), portal venous (PVP) and equilibrium phases (EP), and dynamic pattern was described according to enhancement progression throughout the different phases. Arterial and dynamic enhancement patterns were correlated with chronic liver disease, tumor size and histological differentiation. RESULTS: Most of the nodules were peripherally hyperenhancing (50%) on AP, and partially hyperenhancing on PVP (67.9%) and EP (80.3%). Forty-six (82.1%) IMCCs showed progressive CE, 7 (12.5%) stable CE and 3 (5.4%) wash-out. In normal liver there were 34 nodules with progressive and 3 with stable CE, whereas in chronic liver disease there were 12 IMCCs with progressive, 4 with stable and 3 with washout pattern (p = 0.01); IMCCs with progressive CE were more differentiated than IMCCs with stable CE and wash-out (p = 0.02). CONCLUSIONS: The most prevalent enhancement pattern of IMCCs was arterial rim enhancement followed by progressive and concentric filling. The stable and the washout patterns were more frequent in poorly differentiated IMCCs. Contrast washout was observed only in IMCCs emerging in chronic liver disease with a risk of misdiagnosis with HCC.
- Published
- 2015
37. Video of the Month. Laparoscopic Cholecystectomy for Left-Sided Gallbladder and Hepatic Pedicle
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Clemente, Gennaro, Silvestrini, Nicola, Panettieri, E, De Rose, Agostino Maria, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Clemente, Gennaro, Silvestrini, Nicola, Panettieri, E, De Rose, Agostino Maria, and Clemente, Gennaro (ORCID:0000-0002-8329-5582)
- Abstract
Left-sided gallbladder (LSGB) in a normally positioned liver, namely in the absence of situs inversus viscerum, is a very uncommon condition. Its incidence is reported in the literature between 0.004 and 0.3 % . It is rarely diagnosed by ultrasounds and usually represents an unexpected finding during laparoscopic cholecystectomy for stones. Sometimes, the gallbladder is simply located to the left of an abnormally right-sided round ligament and, in this case, it should be defined as “wrong LSGB”. When the gallbladder is really attached to the left lobe of the liver, it should be defined as “ true LSGB”. More rarely, the hepatic pedicle is also located to the left of the round ligament and the cystic duct joins the CBD from the left side. Anomalies of the biliary and vascular anatomy are frequently associated and, consequently, bile ducts injuries appear to be not infrequent in these cases. A 39-year-old female, without previous medical problems, presented with recurrent biliary pain and evidence of stones in the gallbladder at the ultrasonography. Laparoscopic cholecystectomy was planned with the patient in the American position, supine with the left arm in abduction. After insertion of the camera in the umbilical port, the gallbladder was not found in its natural position, but adherent to the left lobe of the liver. The hepatic pedicle was also located to the left of the umbilical fissure with hepatic artery on the its right edge. The operative trocar was positioned in the left hypocondrium rather than in the epigastrium. After identification of the cystic artery, arising from the hepatic artery, and the cystic duct, these structures were clipped and divided. The CBD was clearly identified. The gallbladder was detached from the liver bed and extracted with a bag. The postoperative course was uneventful and the patient was discharged in the first postoperative day.
- Published
- 2015
38. Parenteral Nutrition in Liver Resection
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Chiarla, Carlo, Giovannini, Ivo, Giuliante, Felice, Ardito, Francesco, Vellone, Maria, De Rose, Agostino Maria, and Nuzzo, Gennaro
- Subjects
Article Subject - Abstract
Albeit a very large number of experiments have assessed the impact of various substrates on liver regeneration after partial hepatectomy, a limited number of clinical studies have evaluated artificial nutrition in liver resection patients. This is a peculiar topic because many patients do not need artificial nutrition, while several patients need it because of malnutrition and/or prolonged inability to feeding caused by complications. The optimal nutritional regimen to support liver regeneration, within other postoperative problems or complications, is not yet exactly defined. This short review addresses relevant aspects and potential developments in the issue of postoperative parenteral nutrition after liver resection.
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- 2012
- Full Text
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39. Sensitivity of Human Intrahepatic Cholangiocarcinoma Subtypes to Chemotherapeutics and Molecular Targeted Agents: A Study on Primary Cell Cultures
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Fraveto, Alice, primary, Cardinale, Vincenzo, additional, Bragazzi, Maria Consiglia, additional, Giuliante, Felice, additional, De Rose, Agostino Maria, additional, Grazi, Gian Luca, additional, Napoletano, Chiara, additional, Semeraro, Rossella, additional, Lustri, Anna Maria, additional, Costantini, Daniele, additional, Nevi, Lorenzo, additional, Di Matteo, Sabina, additional, Renzi, Anastasia, additional, Carpino, Guido, additional, Gaudio, Eugenio, additional, and Alvaro, Domenico, additional
- Published
- 2015
- Full Text
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40. Metabolic consequences of the occlusion of the main pancreatic duct with acrylic glue after pancreaticoduodenectomy
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Mezza, Teresa, primary, Clemente, Gennaro, additional, Sorice, Gian Pio, additional, Conte, Caterina, additional, De Rose, Agostino Maria, additional, Sun, Vincin Alice, additional, Cefalo, Chiara Maria Assunta, additional, Pontecorvi, Alfredo, additional, Nuzzo, Gennaro, additional, and Giaccari, Andrea, additional
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- 2015
- Full Text
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41. Spigelian hernia repair with self-gripping Parietex ProgripTM mesh
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Clemente, Gennaro, De Rose, Agostino Maria, Ionta, Lucia, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Clemente, Gennaro, De Rose, Agostino Maria, Ionta, Lucia, and Clemente, Gennaro (ORCID:0000-0002-8329-5582)
- Abstract
spigelian hernia repair with self-gripping parietex progrip mesh
- Published
- 2014
42. Investigating the Synergistic Interaction of Diabetes, Tobacco Smoking, Alcohol Consumption, and Hypercholesterolemia on the Risk of Pancreatic Cancer: A Case-Control Study in Italy
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La Torre, Giuseppe, primary, Sferrazza, Antonella, additional, Gualano, Maria Rosaria, additional, de Waure, Chiara, additional, Clemente, Gennaro, additional, De Rose, Agostino Maria, additional, Nicolotti, Nicola, additional, Nuzzo, Gennaro, additional, Siliquini, Roberta, additional, Boccia, Antonio, additional, and Ricciardi, Walter, additional
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- 2014
- Full Text
- View/download PDF
43. Chance of cure following liver resection for initially unresectable colorectal metastases: analysis of actual 5-year survival
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Ardito, Francesco, Vellone, Maria, Cassano, Alessandra, De Rose, Agostino Maria, Pozzo, Carmelo, Coppola, Alessandro, Federico, Bruno, Giovannini, Ivo, Barone, Carlo Antonio, Nuzzo, Gennaro, Giuliante, Felice, Ardito, Francesco (ORCID:0000-0003-1596-2862), Vellone, Maria (ORCID:0000-0002-7628-4092), Cassano, Alessandra (ORCID:0000-0002-3311-7163), Giuliante, Felice (ORCID:0000-0001-9517-8220), Ardito, Francesco, Vellone, Maria, Cassano, Alessandra, De Rose, Agostino Maria, Pozzo, Carmelo, Coppola, Alessandro, Federico, Bruno, Giovannini, Ivo, Barone, Carlo Antonio, Nuzzo, Gennaro, Giuliante, Felice, Ardito, Francesco (ORCID:0000-0003-1596-2862), Vellone, Maria (ORCID:0000-0002-7628-4092), Cassano, Alessandra (ORCID:0000-0002-3311-7163), and Giuliante, Felice (ORCID:0000-0001-9517-8220)
- Abstract
Background Survival with long-term follow-up following liver resection for unresectable colorectal liver metastases (CRLM) downsized by chemotherapy has rarely been reported. The aim of this study was to determine the chance of cure following liver resection for initially unresectable CRLM. Methods Between January 2000 and December 2009, 61 patients underwent hepatectomy for unresectable liver-only CRLM downsized after chemotherapy. Cure was defined as a recurrence-free interval of at least 5 years after primary hepatectomy. Results Resectability of CRLM was achieved after a mean number of 11 courses, and 42.6 % of patients underwent liver resection after ≥10 courses. Postoperative mortality was nil, and morbidity rate was 19.7 %. The 5- and 10-year actuarial overall survival rates were 42.6 and 16.0 %. Of 30 patients with a follow-up ≥5 years, 11 were alive, yielding a 5-year actual overall survival rate of 36.7 %, and 7 (23.3 %) were considered cured because they are alive without recurrence. On multivariate analysis, response to chemotherapy was the only independent predictor of both overall and disease-free survival. Conclusions Cure can be achieved in about 23 % of patients resected for initially unresectable CRLM downsized by chemotherapy. Liver resection can be safely performed in selected patients even after multiple courses of chemotherapy.
- Published
- 2013
44. Lymphoepithelial cyst of the pancreas: case report and review of the literature
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Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, Giordano, Marco, Ricci, Riccardo, Vecchio, Fabio Maria, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Ricci, Riccardo (ORCID:0000-0002-9089-5084), Vecchio, Fabio Maria (ORCID:0000-0002-9197-2264), Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, Giordano, Marco, Ricci, Riccardo, Vecchio, Fabio Maria, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Ricci, Riccardo (ORCID:0000-0002-9089-5084), and Vecchio, Fabio Maria (ORCID:0000-0002-9197-2264)
- Abstract
BACKGROUND AND STUDY AIMS: Lymphoepithelial cyst of the pancreas (LCP) is a rare, benign cyst mimicking pseudocyst or cystic neoplasm. Literature describing LCP is limited to case or brief series reports, and the natural history of this condition is largely unknown. A literature review was carried out in order to elucidate the clinical, pathological and biochemical features of LCP. The aim of this study was to define diagnostic criteria and treatment. METHODS: A Medline and Pubmed search was conducted by using the key-words "lymphoepithelial cyst" and "pancreas". The articles found were accurately examined and all details regarding clinical and pathological features were included in a data-base. Furthermore, a case recently observed in our unit was added to the review. RESULTS: Ninety-two cases of LCP were found in the worldwide literature, including the case that we observed. LCP occurs more frequently in males (M:F=5.5:1), its preferred site is the tail of the pancreas, and its size ranges between 2 and 10centimetres. Histologically, it is a true cyst delineated by a keratinizing squamous epithelium surrounded by lymphoid tissue. LCP is asymptomatic in the majority of cases and preoperative diagnosis is complicated by a lack of specific radiological features of the disease. An accurate preoperative diagnosis can only be made by obtaining cytological specimens and placing them in the hands of a pathologist who is familiar with the cytological appearances of the disease. CONCLUSIONS: LCP is a rare lesion worldwide, without any prevalence in different countries or in different ethnic groups. Understanding the features of LCP, making an accurate diagnosis and differentiating it from cystic neoplasm preoperatively is vital, as when it is diagnosed certainly, a conservative treatment is justified. Otherwise, radical surgery in the form of pancreatic resection is required to exclude the diagnosis of pancreatic cystic neoplasm.
- Published
- 2011
45. Image of the month: metastasis from leiomyosarcoma in the head of the pancreas
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Clemente, Gennaro, Giordano, Marco, De Rose, Agostino Maria, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Clemente, Gennaro, Giordano, Marco, De Rose, Agostino Maria, Nuzzo, Gennaro, and Clemente, Gennaro (ORCID:0000-0002-8329-5582)
- Abstract
No Abstract
- Published
- 2010
46. Résections hépatiques pour lithiases sur dilatations congénitales des voies biliaires intrahépatiques
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Clemente, Gennaro, Giuliante, Felice, De Rose, Agostino Maria, Ardito, Francesco, Giovannini, Ivo, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Giuliante, Felice (ORCID:0000-0001-9517-8220), Ardito, Francesco (ORCID:0000-0003-1596-2862), Clemente, Gennaro, Giuliante, Felice, De Rose, Agostino Maria, Ardito, Francesco, Giovannini, Ivo, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Giuliante, Felice (ORCID:0000-0001-9517-8220), and Ardito, Francesco (ORCID:0000-0003-1596-2862)
- Abstract
Objectif.— Cette étude rapporte une expérience clinique relative aux résections hépatiques pour dilatations congénitales des voies biliaires et lithiase intrahépatique associée pour évaluer les résultats et définir les indications du traitement. Patients et méthodes.— Nous avons étudié les données cliniques des patients soumis à une résection hépatique de janvier 1992 à décembre 2008 et évalué les résultats immédiats et cela à distance des interventions. Résultats.— Sur 49 patients traités, 47 ont eu une résection hépatique. Dans la majorité des cas la maladie était limitée au foie gauche et l’hépatectomie gauche a été l’intervention chirurgicale la plus fréquente. La mortalité opératoire a été nulle et la morbidité de 24,5 %. Un cholangiocarcinome a été diagnostiqué dans six cas (12,2 %). Dans 91,6 % de cas, les résultats à distance ont été bons ou satisfaisants. Conclusion.— Les objectifs du traitement doivent être dans tous les cas l’élimination des calculs, la prévention des récidives ainsi que celle du cholangiocarcinome. La chirurgie d’exérèse représente le meilleur traitement possible pour les patients symptomatiques avec une maladie localisée et atrophie du foie touché.
- Published
- 2010
47. Liver resection for intrahepatic stones in congenital bile duct dilatation
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Clemente, Gennaro, Giuliante, Felice, De Rose, Agostino Maria, Ardito, Francesco, Giovannini, Ivo, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Giuliante, Felice (ORCID:0000-0001-9517-8220), Ardito, Francesco (ORCID:0000-0003-1596-2862), Clemente, Gennaro, Giuliante, Felice, De Rose, Agostino Maria, Ardito, Francesco, Giovannini, Ivo, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Giuliante, Felice (ORCID:0000-0001-9517-8220), and Ardito, Francesco (ORCID:0000-0003-1596-2862)
- Abstract
Objective: This study reports our clinical experience with liver resection for congenital dilatation of the intrahepatic bile duct and intrahepatic gallstones to evaluate results and define indications for treatment. Patients and methods: We studied the clinical data of patients who underwent hepatic resection for intrahepatic lithiasis from January 1992 to December 2008 and assessed the immediate and long-term results of these interventions. Results: Of 49 treated patients, 47 underwent liver resection. In the majority of cases, the disease was limited to the left lobe and left hepatectomy was the most commonly performed surgical procedure. The operative mortality was zero with morbidity in 24.5% of patients. Cholangiocarcinoma was diagnosed in six cases (12.2%). In 91.6% of cases the long-term results were good or satisfactory. Conclusion: Treatment goals in all cases should be the elimination of intrahepatic stones, the prevention of recurrent lithiasis, and prevention or cure of cholangiocarcinoma. Surgical excision is the best possible treatment for symptomatic patients with localized disease and atrophy of the affected liver
- Published
- 2010
48. Gas in portal circulation and pneumatosis cystoides intestinalis during chemotherapy for advanced rectal cancer
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Clemente, Gennaro, Chiarla, Carlo, Giovannini, Ivo, De Rose, Agostino Maria, Astone, Antonio, Barone, Carlo Antonio, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Chiarla, Carlo (ORCID:0000-0001-9403-433X), Astone, Antonio (ORCID:0000-0001-9572-309X), Clemente, Gennaro, Chiarla, Carlo, Giovannini, Ivo, De Rose, Agostino Maria, Astone, Antonio, Barone, Carlo Antonio, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Chiarla, Carlo (ORCID:0000-0001-9403-433X), and Astone, Antonio (ORCID:0000-0001-9572-309X)
- Abstract
OBJECTIVES: Acute abdominal symptoms with CT scan evidence of intramural gas in bowel walls (pneumatosis cystoides intestinalis, PCI) and of gas in the portal venous blood (PBG) in patients undergoing chemotherapy may represent a worrisome picture, suggestive of bowel necrosis. This picture remains a major clinical clue and the reporting of new cases may help to share awareness and experience on management. We describe a patient with acute abdominal symptoms and evidence of PCI with PBG under cetuximab, oxaliplatin, tegafur-uracil and folinic acid chemotherapy for metastatic adenocarcinoma of the rectosigmoid junction. METHODS: After admission for mucositis with diarrhea and profound dehydration, and subsequent emergency laparotomy for derotation of an intestinal volvulus, on the tenth postoperative day the patient developed fever and abdominal pain, with CT scan evidence of PCI with PBG. The exam of the abdomen did not suggest major problems requiring emergency surgery, and antibiotic treatment with close monitoring were performed, followed by rapid improvement. RESULTS: Twelve days later, after resumption of oral diet, the patient unexpectedly suffered a spontaneous jejunal microperforation, requiring emergency laparotomy and bowel resection. Pathology showed that the perforation was within an area of ulceration involving the inner superficial layer of the bowel. Subsequently recovery was normal and at present, after 15 months, the patient is well and continuing chemotherapy. CONCLUSIONS: This is probably the first report of PCI with PBG related to intestinal toxicity during cetuximab, oxaliplatin, tegafur-uracil and folinic acid chemotherapy in a patient with advanced rectal carcinoma, followed by delayed small bowel perforation. It provides an example of the challenges involved in the management of this type of patient.
- Published
- 2010
49. Unexpected diagnosis of Crohn’s disease after the ingestion of a dental bridge
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Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, Mele, Carmela, Ranucci, Giuseppina, Nuzzo, Gennaro, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, Mele, Carmela, Ranucci, Giuseppina, Nuzzo, Gennaro, and Clemente, Gennaro (ORCID:0000-0002-8329-5582)
- Abstract
No abstract. The report deals with the unexpected diagnosis of Crohn's disease, when a patient ingested a dental bridge which caused bowel occlusion and underwent surgery
- Published
- 2009
50. Electronic clinical challenges and images in GI. Giant gastric polyp prolapsing into the duodenum
- Author
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Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, Clemente, Gennaro (ORCID:0000-0002-8329-5582), Clemente, Gennaro, Sarno, Gerardo, De Rose, Agostino Maria, and Clemente, Gennaro (ORCID:0000-0002-8329-5582)
- Abstract
No Abstract
- Published
- 2009
- Full Text
- View/download PDF
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