Results 11 to 20 of about 165,950,413 (205)

Signet ring carcinoma of ampulla of vater

Advanced Biomedical Research, 2014
Signet ring carcinoma is a common type of adenocarcinoma of stomach but its occurrence in ampulla of Vater is extremely rare. There are only a few previous reported cases of signet ring carcinoma of ampulla of Vater.
Ardeshir Talebi, Fareshteh Mohammadizadeh, Mohsen Hani, Marzie Bagheri, Azam Bagheri   +4 more
doaj   +2 more sources

Signet Ring Cell Carcinoma of the Ampulla of Vater: A Rare Histopathological Variant [PDF]

Case Reports in Gastroenterology, 2018
Signet ring cell carcinoma (SRCC) of the ampulla of Vater is an extremely rare tumor. Our case describes a 45-year-old female presenting with jaundice and pruritus. Computed tomography, endoscopy, and endoscopic retrograde cholangiopancreatography showed
Guus W. de Klein, Joop van Baarlen, Leonie J. Mekenkamp, Mike S.L. Liem, Joost M. Klaase   +4 more
doaj   +3 more sources

Signet-Ring Cell Carcinoma of the Ampulla of Vater [PDF]

The Indonesian Journal of Gastroenterology, Hepatology and Digestive Endoscopy, 2018
Signet-ring cell carcinoma (SRCC) of the ampulla of Vater is a very rare case and only 28 cases have beed reported in the English literature. Herein, we report a 59-year-old woman with SRCC of the ampulla of Vater.
Lianda Siregar, Imelda M Loho, Agus Sudiro Waspodo, Dwi Sri Rejeki, Fajar Firsyada, Rahmanandika Swadari, Getty Inash Nandika, Muhammad Iqbal Siregar   +7 more
doaj   +2 more sources

FLUCTUATING JAUNDICE IN THE ADENOCARCINOMA OF THE AMPULLA OF VATER: a classic sign or an exception?

Arquivos de Gastroenterologia, 2015
Background Some authors consider the fluctuating jaundice as a classic sign of the adenocarcinoma of the ampulla of Vater. Objetive Assessing the frequency of fluctuating jaundice in their forms of its depiction in the patients with adenocarcinoma of the
José Roberto ALVES, Enio Campos AMICO, Dyego Leandro Bezerra de SOUZA, Patrick Vanttinny Vieira de OLIVEIRA, Ícaro Godeiro de Oliveira MARANHÃO   +4 more
doaj   +2 more sources

A case of gangliocytic paraganglioma in the ampulla of Vater [PDF]

World Journal of Surgical Oncology, 2010
Background Duodenal gangliocytic paraganglioma is an extremely rare tumor and few cases have been reported to date. Case presentation The authors report a case of gangliocytic paraganglioma verified by post-op pathology after pancreaticoduodenectomy for ...
Jang Jin-Young, Kang Mee, Lee Seung, Kwon Junsik, Kim Sun-Whe   +4 more
doaj   +2 more sources

Primary large B-cell lymphoma of the ampulla of Vater

Haematologica, 2006
Primary lymphoma of the ampulla of Vater is rare. The clinico-pathological and interesting endoscopic and radiological features of a patient with this disorder is presented.
CS Chim, WK Yuen, F Loong, WH Hu, GC Ooi
doaj   +1 more source

Hodgkin lymphoma of the ampulla of Vater: A rare cause of obstructive jaundice in children. [PDF]

JPGN Rep
Abstract Hodgkin lymphoma (HL) has a wide spectrum of presentation. Most cases affect lymph nodes (nodal), while extranodal involvement is rare. Whereas the gastrointestinal tract is enriched with lymphoid tissues, the ampulla of Vater is not rich in lymphoid tissue. Involvement of the ampulla of Vater with HL has rarely been reported in adults and has
Alshammari S, Alhebbi H, Al Qahtani A, Algubaisi S, Alhaffaf F, Al Robayan A, Almutairi M, Alshieban S, Alshahrani M, Alfawzan TK, Alkhamis K, Al Hasan I, Wali S.   +12 more
europepmc   +2 more sources

Neuroendocrine Tumor of the Ampulla of Vater: A Case Report. [PDF]

Cureus, 2023
Neuroendocrine tumors (NETs) of the ampulla of Vater are extremely rare. Here, we discuss the clinical presentation, diagnostic challenges, and treatment options of a recently experienced case of NET of the ampulla of Vater in light of the literature.
Aman MS, Das BC, Islam A, Arefin M, Gupta SN.   +4 more
europepmc   +2 more sources

Readmission rate and complications following biopsy of the ampulla of Vater—A retrospective data analysis [PDF]

JGH Open, 2023
Kim Hay Be, Sam Rosella
exaly   +2 more sources

Large cell neuroendocrine carcinoma of the ampulla of Vater. [PDF]

, 2012
Large cell neuroendocrine carcinomas of the ampulla of Vater are rare and confer a very poor prognosis despite aggressive therapy. There are few case reports of large cell neuroendocrine carcinomas of the ampulla of Vater in the literature and to date no
Beggs, Rachel E, Eltayeb, Omer, Ridgway, Paul F, Kelly, Michael E, Crotty, Paul, McDermott, Ray   +5 more
core   +2 more sources