Results 41 to 50 of about 3,575 (179)

The enigma of struma ovarii [PDF]

open access: yes, 2007
Since its first description in the early part of the twentieth century, struma ovarii has elicited considerable interest because of its many unique features; however, at present a number of aspects remain enigmatic.
Roth, Lawrence M., Talerman, Aleksander
core   +2 more sources

A rare goblet cell adenocarcinoma arising from Barrett’s esophagus: the first reported case in the esophagus [PDF]

open access: yesJournal of Pathology and Translational Medicine
Goblet cell adenocarcinoma (GCA) is a rare and distinctive amphicrine tumor comprised of goblet-like mucinous cells and neuroendocrine cells. It is believed to originate from pluripotent stem cells located at the base of crypts.
Chi Eun Oh, Sung Eun Kim, Sun-Ju Oh
doaj   +1 more source

Perforated mixed carcinoid-adenocarcinoma in transverse colon and at gastroenterostomy site: case report

open access: yesWorld Journal of Surgical Oncology, 2010
Goblet cell carcinoid of the large intestine is a rare neoplasm, usually located in ascending colon and rectum. A 60-year-old male patient underwent surgery after the diagnosis of acute abdomen. Exploratory laparotomy revealed perforation with a diameter
Karakaş Barış R   +4 more
doaj   +1 more source

An Unusual Case of Synchronous Carcinoid of Ovary and Gall Bladder [PDF]

open access: yes, 2013
Multifocal carcinoid is a known phenomenon. We present a rare combination of an ovarian carcinoid synchronous with gallbladder carcinoid. This rare combination has not been reported so far.
Nita Khurana   +3 more
core   +2 more sources

Neuroendocrine neoplasms of the digestive system – current classification and terminology

open access: yesNowotwory, 2021
The system of classification and terminology of neuroendocrine neoplasms (NENs), updated in 2017 by AJCC and in 2019 by WHO, is now recommended for general use.
Agata Bałdys-Waligórska, Andrzej Nowak
doaj   +1 more source

Are goblet cell carcinoids a group of heterogeneous tumors?

open access: yesBiomedical Papers, 2017
Background: Goblet cell carcinoids belong to neuroendocrine tumors, according to the WHO classification. The tumors are diagnosed based on a typical histological pattern and using neuroendocrine markers.
Jirka Macak   +2 more
doaj   +1 more source

Clinicopathologic Study of Appendix Specimens- A Two Year Retrospective Study at a Tertiary Care Center [PDF]

open access: yesNational Journal of Laboratory Medicine, 2019
Introduction: Acute appendicitis is the most common abdominal emergency and has remained an on going diagnostic challenge. Histopathologic studies are the gold standard for final diagnosis. Aim: To study the histopathological features of appendix and
Aneel Myageri   +2 more
doaj   +1 more source

Classification of mucinous appendiceal neoplasm and pseudomyoxma peritonei

open access: yesJournal of Pathology of Nepal, 2018
Mucinous appendiceal tumors are uncommon and include a wide spectrum of tumors whose classification remained controversial. Some of these mucin producing appendiceal tumors can disseminate to the peritoneal cavity leading to pseudomyxoma peritonei (PMP).
Arnab Ghosh
doaj   +1 more source

Neuroendocrine tumors of the gallbladder: a case report and review of the literature [PDF]

open access: yes, 2011
Introduction. Primary gallbladder neuroendocrine tumors are extremely rare, representing 0.2% of all neuroendocrine tumors. The diagnosis is incidental in most cases. Case presentation.
Cimadon, B   +7 more
core   +2 more sources

Fístula vésico-apendicular em adenocarcinoma mucinoso do apêndice [PDF]

open access: yes, 2008
BACKGOUND: A rare case of vesicoappendiceal fistula secondary to mucinous adenocarcinoma of the appendix is presented. CASE REPORT: A 62-year-old man with a one year history of recurrent urinary tract infections. After two months he developed pneumaturia
COCUZZA, Marcello   +6 more
core   +2 more sources

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