نتایج جستجو برای: neuroendocrine tumor

تعداد نتایج: 443250  

2010
Jie Chen Ling Zhang Wenjun Zhang Weiqiang Zheng Duowu Zou Zhaoshen Li

The diagnosis of neuroendocrine malignant tumor in the small bowel is difficult [J Oncol 2008;2008:212067]. It is usually found intraoperatively during intestinal resection and confirmed by subsequent histological examination. We reported a case of jejunum neoplasm which was misdiagnosed as Crohn's disease by capsule endoscopy. Capsule endoscopy was stuck in the jejunum stricture and was remove...

Journal: :Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2013
Tuba Bayındır Neşe Karadağ Erkan Karataş Ahmet Kızılay

Neuroendocrine tumors of the larynx are rarely seen neoplasms. Atypical carcinoid tumor is the most common type of the neuroendocrine tumors of the larynx, whereas the typical carcinoid tumor is the most infrequent type. Preferable treatment in typical carcinoid tumor is particularly conservative surgery without neck dissection. Radio-chemotherapy is ineffective. In this report, we present a 61...

Journal: :Collegium antropologicum 2012
Zvonko Zadro Jurica Fudurić Ivan Frketić Sanja Stifter Tatjana Bujas Ana Sostarić Zadro Zoran Veir Ines Doko

Neuroendocrine tumors are very rare tumors that occur most commonly in the gastrointestinal tract. The occurrence of neuroendocrine tumors outside gastrointestinal tract is very rare but not unknown. Thus, neuroendocrine tumors and their primary seat can be found in the bronchi and lungs, as well as in the testicles, ovaries, prostate, etc. The occurrence of neuroendocrine tumors as a primary s...

2012
Wyatt Unger Qian Tang Danielle Summers Wenxin Zheng

This is the first reported case, to our knowledge, of a true collision primary tumor of the endometrium. Neuroendocrine carcinoma of the endometrium is itself a rare tumor. In this case we present a collision tumor of neuroendocrine carcinoma with endometrioid adenocarcinoma of the endometrium. The unique morphologic and immunophenotypic features of these tumors in this case are discussed, just...

Journal: :Clinical chemistry 2007
Tine Børglum Jens F Rehfeld Lars B Drivsholm Linda Hilsted

BACKGROUND Most neuroendocrine tumors express chromogranin A (CgA). The posttranslational processing of neuroendocrine proteins such as CgA is often specific for the individual tumor. To cope with this variability and improve tumor diagnosis, we developed a processing-independent analysis (PIA) method to measure the total CgA product. METHODS For PIA, samples underwent trypsin treatment follo...

Journal: :Journal of the Chinese Medical Association : JCMA 2008
Shih-Hao Liu Shyh-Haw Tsay

We report a case of coexisting poorly differentiated endocrine carcinoma and conventional adenocarcinoma in the ampulla of Vater. A 70-year-old female had a recent history of symptoms and signs related to obstructive jaundice. An initial endoscopic biopsy of the ampulla of Vater showed a poorly differentiated endocrine carcinoma in the lamina propria of duodenal mucosa. The tumor could also be ...

2015
Nicola Fusco Elena Guerini-Rocco Alessandro Del Gobbo Renato Franco Federica Zito-Marino Valentina Vaira Gaetano Bulfamante Giulia Ercoli Mario Nosotti Alessandro Palleschi Silvano Bosari Stefano Ferrero Giancarlo Troncone

Lung cancer encompasses a constellation of malignancies with no validated prognostic markers. p16Ink4A expression has been reported in different subtypes of lung cancers; however, its prognostic value is controversial. Here, we sought to investigate the clinical significance of p16Ink4A immunoexpression according to specific staining patterns and its operational implications. A total of 502 tum...

Journal: :Hpb 2021

Introduction: Neuroendocrine tumors(NET) represent rare neoplasms with majority primary NETs being gastroenteropancreatic or bronchopulmonary origin. A hepatic NET is most likely a metastastic lesion. Cystic lesions are commonly either infectious, benign cystic lesions, if malignant; cystadenocarcinoma, hepatocellular carcinoma, metastasis degeneration. Primary neuroendocrine tumors(PHNETs) and...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2016
Om Parkash Adil Ayub Buria Naeem Sehrish Najam Zubair Ahmed Wasim Jafri Saeed Hamid

Primary Hepatic Carcinoid Tumor (PHCT) represents an extremely rare clinical entity with only a few cases reported to date. These tumors are rarely associated with metastasis and surgical resection is usually curative. Herein, we report two cases of PHCT associated with poor outcomes due to late diagnosis. Both cases presented late with non-specific symptoms. One patient presented after a 2-wee...

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