Results 11 to 20 of about 470,249 (222)

Neuroendocrine neoplasms of the duodenum, ampullary region, jejunum and ileum [PDF]

Pathologica, 2021
Summary Neuroendocrine neoplasms of the small intestine are some of the most frequently occurring along the gastrointestinal tract, even though their incidence is extremely variable according to specific sites.
M. Milione, P. Parente, F. Grillo, G. Zamboni, L. Mastracci, C. Capella, M. Fassan, A. Vanoli   +7 more
semanticscholar   +2 more sources

Testicular Metastasis of Jejunal Neuroendocrine Tumor on 68Ga-DOTATATE PET/CT

Molecular Imaging and Radionuclide Therapy, 2023
Neuroendocrine tumors are slow-growing tumors originating from neuroendocrine cells and capable of metastasis. Most of them are found in the gastrointestinal tract; however, they can also be rarely seen in other organs.
Ö. Şahin, Özge Erol Fenercioğlu, E. Beyhan, T. Çermik, N. Ergül   +4 more
semanticscholar   +2 more sources

An Unusual Case of Pleuropulmonary Blastoma in a Child with Jejunal Hamartomas [PDF]

Case Reports in Pediatrics, 2013
We report a rare case of 9-month-old girl who presented with a choking episode and was found to have an incidental finding of a lung cyst and iron deficiency anemia leading to the diagnosis of pleuropulmonary blastoma (PPB) and a jejunal hamartoma.
Chantal Lucia-Casadonte, Sakil Kulkarni, Ricardo Restrepo, Ruben Gonzalez-Vallina, Carole Brathwaite, Edward Y. Lee   +5 more
doaj   +2 more sources

Multiple Primary Malignant Neoplasms in the Presence of Concomitant Chilaiditi Syndrome

Turkish Journal of Colorectal Disease, 2018
Chilaiditi syndrome, jejunal diverticulosis, and multiple primary malignant neoplasms (MPMN) are all relatively rare entities. In this study, clear cell renal cell carcinoma together with adenocarcinoma arising in the rectum were confirmed in an 82-year ...
Ali Ezer, Alper Parlakgümüş
doaj   +2 more sources

Jejunal gastrointestinal stromal tumors mimicking arteriovenous malformation: A review of the literature

Annals of the National Academy of Medical Sciences (India)
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal neoplasms that may arise anywhere along the gastrointestinal tract. While most GISTs remain asymptomatic, presentation with acute, massive gastrointestinal hemorrhage is uncommon. An even rarer
A. Nayyar, Vibha Singh, Adiba Nizam, A. Mishra   +3 more
semanticscholar   +2 more sources

Perforated Jejunal Adenocarcinoma in a COVID-19-Positive Patient*

Journal of Coloproctology, 2021
Jejunal adenocarcinoma is a rare type of primary small bowel malignancy. It is generally diagnosed at late stages and as a surgical finding, with abdominal pain or discomfort being the main associated symptom.
Jorge Said Haro Cruz, Ana Cristina Díaz Degollado, Ricardo García Iturbide, Claudio Daniel Rojas Gutiérrez, Javier Alba Macías, Andrei Coria Hernández   +5 more
doaj   +1 more source

Disseminated Angiosarcoma With Multifocal Small-Bowel Involvement Presenting as Suspected Small-Bowel Bleeding. [PDF]

DEN Open
ABSTRACT Angiosarcoma is a rare, aggressive vascular malignancy, and gastrointestinal involvement is uncommon. We report disseminated angiosarcoma with multifocal small‐bowel involvement presenting as suspected small‐bowel bleeding, in which small‐bowel capsule endoscopy (SBCE) and double‐balloon endoscopy (DBE) were diagnostically useful. A man in his
Tomita M, Tashiro T, Yamaguchi Y, Adachi K, Ebi M, Ogasawara N, Sasaki M, Hinokimoto A, Tsuzuki T, Nakamura M.   +9 more
europepmc   +2 more sources

Intraductal papillary mucinous neoplasm originating from a jejunal heterotopic pancreas: A case report

World Journal of Clinical Cases, 2023
Intraductal papillary mucinous neoplasm (IPMN) is a rare pancreatic tumor and has the potential to become malignant. Surgery is the most effective treatment at present, but there is no consensus on the site of resection. Heterotopic pancreas occurs in the gastrointestinal tract, especially the stomach and duodenum but is asymptomatic and rare.
Huang, Jun-Hao, Guo, Wei, Liu, Zhe
openaire   +2 more sources

A giant jejunal gastrointestinal stromal tumor misconceived as pancreatic cystic neoplasm [PDF]

International Journal of Surgery Case Reports, 2019
Abstract Introduction Gastrointestinal stromal tumors (GISTs), although not common in gastrointestinal (GI) tumors, constitute the most frequent mesenchymal tumors of the GI tract. This report describes a patient with a large sporadic GIST at proximal jejunum that mimicked the pancreatic cystic
Wongta, Kitti, Tangsirapat, Vorapatu, Chakrapan Na Ayudhya, Vichack, Charutragulchai, Papot, Sripreechapattana, Singha, Chakrapan Na Ayudhya, Kobkool, Poolsavatkitikool, Rapol, Sookpotarom, Paiboon, Vejchapipat, Paisarn   +8 more
openaire   +2 more sources

European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender

BJS (British Journal of Surgery), EarlyView., 2020
Recommendations for clinical and molecular identification of LS, surgical and endoscopic management of LS‐associated colorectal cancer and preventive measures for cancer were produced. The emphasis was on surgical and gastroenterological aspects of the cancer spectrum.
T. T. Seppälä, A. Latchford, I. Negoi, A. Sampaio Soares, R. Jimenez‐Rodriguez, L. Sánchez‐Guillén, D. G. Evans, N. Ryan, E. J. Crosbie, M. Dominguez‐Valentin, J. Burn, M. Kloor, M. von Knebel Doeberitz, F. J. B. van Duijnhoven, P. Quirke, J. R. Sampson, P. Møller, G. Möslein, on behalf of the European Hereditary Tumour Group (EHTG) and European Society of Coloproctology (ESCP)   +18 more
wiley   +1 more source