Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zisis Touloumis"'
Publikováno v:
Case Reports in Oncological Medicine, Vol 2013 (2013)
Introduction. Pseudomyxoma peritonei (PMP) is an uncommon surgical entity. We report a case of aggressive disease with an unusual clinical presentation and we analyze current data on diagnosis and management of PMP. Case Presentation. A 71-year-old m
Externí odkaz:
https://doaj.org/article/a1a66149700645808fa2a91888fb5744
Extra-Gastrointestinal Stromal Tumor of the Omentum: A Rare Case Report and Review of the Literature
Autor:
Dimitris Fagkrezos, Zisis Touloumis, Maria Giannila, Charalampos Penlidis, Kleo Papaparaskeva, Charikleia Triantopoulou
Publikováno v:
Rare Tumors, Vol 4 (2012)
Gastrointestinal stromal tumors (GIST) are uncommon mesenchymal spindle-cell or epithelioid neoplasms, located mainly with higher frequency in the stomach and small bowel. GISTs represent the majority of primary non-epithelial neoplasms of the digest
Externí odkaz:
https://doaj.org/article/32826a2a685947bfa2b6ac4013918ec2
Autor:
John Griniatsos, Niki Giannakou, Zisis Touloumis, Argiro Trigka, Christos Sioros, Maria Cheilakea, Nikoletta Dimitriou
Publikováno v:
World Journal of Clinical Cases
BACKGROUND The perivascular epithelioid cell tumour (PEComa) family of tumours mainly includes renal and hepatic angiomyolipomas, pulmonary lymphangioleiomyomatosis and clear cell “sugar” tumour of the lung. Several uncommon tumours with similar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d0b022cd38191c8237312d1f9b7ed4e
https://doi.org/10.12998/wjcc.v7.i21.3507
https://doi.org/10.12998/wjcc.v7.i21.3507
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 25(5)
To investigate the expressions of caspase-3 and survivin in colorectal cancer patients and their possible associations with clinicopathological parameters and the oncological outcome.Between January 2008 and December 2011, 85 patients with sporadic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db2d754d8f7b1677959d1cd3dc178a71
https://pubmed.ncbi.nlm.nih.gov/33277831
https://pubmed.ncbi.nlm.nih.gov/33277831
Autor:
George Galyfos, Nikolaos Kavouras, Maria Chalasti, Zisis Touloumis, Laurant Lavant, Konstantinos Stergios, Konstantinos Palogos
Publikováno v:
International Journal of Surgery Case Reports. 5:104-107
INTRODUCTION Pseudocysts of the spleen are usually asymptomatic and associated with a history of trauma, infection or infarction. In this report, we present two uncommon cases of solitary, oversized pseudocysts of the spleen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f0ba86cc4ad7186b657f36c849c831d
https://doi.org/10.1016/j.ijscr.2013.11.006
https://doi.org/10.1016/j.ijscr.2013.11.006
Autor:
George, Galyfos, Zisis, Touloumis, Konstantinos, Palogos, Konstantinos, Stergios, Maria, Chalasti, Nikolaos, Kavouras, Laurant, Lavant
Publikováno v:
International Journal of Surgery Case Reports
INTRODUCTION Pseudocysts of the spleen are usually asymptomatic and associated with a history of trauma, infection or infarction. In this report, we present two uncommon cases of solitary, oversized pseudocysts of the spleen. PRESENTATION OF CASE Two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f0f81cbf2a59e6be32891698e28efac
https://pubmed.ncbi.nlm.nih.gov/24463562
https://pubmed.ncbi.nlm.nih.gov/24463562
Extra-gastrointestinal stromal tumor of the omentum: a rare case report and review of the literature
Autor:
Maria Giannila, Dimitris Fagkrezos, Charikleia Triantopoulou, Zisis Touloumis, Charalampos Penlidis, Kleio Papaparaskeva
Publikováno v:
Rare Tumors
Rare Tumors, Vol 4 (2012)
Rare Tumors, Vol 4, Iss 3 (2012)
Rare Tumors, Vol 4 (2012)
Rare Tumors, Vol 4, Iss 3 (2012)
Gastrointestinal stromal tumors (GIST) are uncommon mesenchymal spindle-cell or epithelioid neoplasms, located mainly with higher frequency in the stomach and small bowel. Gastrointestinal stromal tumors (GISTs) represent the majority of primary non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c405f341c910377f13c23a39fd2458c3
http://europepmc.org/articles/PMC3475951
http://europepmc.org/articles/PMC3475951
Autor:
Zisis Touloumis, Nikoletta Giannakou, Christos Dervenis, Charikleia Triantopoulou, Spiros Delis, Costas Avgerinos
Publikováno v:
Cases Journal
Introduction Primary hepatic carcinoid tumours (PHCTs) are extremely rare neuroendocrine neoplasms. Only 58 cases have been reported in the literature and less than 10 cases were functional. Case presentation We present a case of a 65 years old, Cauc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35d9dab952256e37c141ba8845f63f5a
https://doi.org/10.1186/1757-1626-1-314
https://doi.org/10.1186/1757-1626-1-314
Autor:
Alexandros, Koliopanos, Constantinos, Avgerinos, Constantina, Paraskeva, Zisis, Touloumis, Dionisisa, Kelgiorgi, Christos, Dervenis
Publikováno v:
Hepatobiliarypancreatic diseases international : HBPD INT. 7(4)
Pancreatic cancer (PCa) is one of the most aggressive human solid tumors, with rapid growth and metastatic spread as well as resistance to chemotherapeutic drugs, leading rapidly to virtually incurable disease. Over the last 20 years, however, signif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83f87cefe33afa8b02bb10d1d35f9a7d
https://pubmed.ncbi.nlm.nih.gov/18693168
https://pubmed.ncbi.nlm.nih.gov/18693168
Autor:
Kostas Athanassiou, Spiros Delis, Nikos Tassopoulos, Konstantina D. Paraskeva, Christos Dervenis, Zisis Touloumis, Andreas Bakoyiannis, Michael Safioleas
Publikováno v:
European journal of gastroenterologyhepatology. 20(1)
Intrahepatic biliary cystadenoma (IBC) is a rare liver tumour, which has strong tendency to recur and malignant potential as it can progress to cystadenocarcinoma (IBCa).From June 2003 to December 2006, four patients diagnosed with hepatic cystadenom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3bbcc7c4a4b2f65f75b6339d0e94c71
https://pubmed.ncbi.nlm.nih.gov/18090983
https://pubmed.ncbi.nlm.nih.gov/18090983