نتایج جستجو برای: primary hepatic neuroendocrine tumor

تعداد نتایج: 1115213  

2009
Kyoung-Won Yoon Chang-Hwan Park Wan-Sik Lee Young-Eun Joo Hyeun-Soo Kim Sung-Kyu Choi Jong-Sun Rew Jae-Hyug Lee

Primary neuroendocrine carcinoma of the gallbladder is extremely rare because normal gallbladder mucosa does not contain neuroendocrine cells. Neuroendocrine cells can be detected at sites of intestinal metaplasia induced by chronic inflammation, which may be the initial step in the development of neuroendocrine tumor of the gallbladder. Anomalous union of the pancreaticobiliary duct (AUPBD) is...

Journal: :The Korean Journal of Gastroenterology 2018

Journal: :The Journal of Association of Chest Physicians 2016

Journal: :QJM : monthly journal of the Association of Physicians 1996
J K Ramage R Williams M Buxton-Thomas

Functional imaging of neuroendocrine tumours with Octreoscan and I123-metaiodobenzylguanidine (MIBG) is important for assessment prior to various therapies and assessing response. The two imaging methods have not been directly compared in hepatic neuroendocrine tumours. Patients (n = 18) were studied with both imaging techniques. The sensitivity of Octreoscan was 94%, and that of MIBG 39%. No p...

Journal: :International Journal of Surgery Case Reports 2019

2010
Stefania Nicoletti Maximilian Papi Fabrizio Drudi Manuela Fantini Debora Canuti Emiliano Tamburini Cinzia Possenti Enzo Pasquini Massimo Brisigotti Alberto Ravaioli

INTRODUCTION Small cell neuroendocrine cancer of the breast is a rare tumor with less than 30 cases reported in the literature. The morphological and immunohistochemical patterns of this tumor are similar to small cell neuroendocrine cancer of the lung. For this reason, it is often difficult to distinguish a primary small cell neuroendocrine cancer of the breast from a metastatic lesion from ot...

2014
Shakir Alsharif Mubarak Al-Shraim Ahmed Alhadi Abdulrahman Al-Aown Fawzy Fooshang Refat Eid

Testicular neuroendocrine tumor is rare. It accounts for less than 1% of all testicular neoplasms. More than 60 cases have been published in the literature. A 27-year-old man presented with left testicular mass and underwent radical orchidectomy. Histological examination showed neuroendocrine tumor, confirmed by immunohistochemistry and electron microscopy. The patient showed no evidence of met...

2013
KONSTANTINOS KOUTSAMPASOPOULOS ELISAVET ANTONIADOU STAVROS ZOUTIS GRIGORIOS IACOVIDIS OLGA BUROVA ANTONIOS TAPLIDIS

Neuroendocrine tumors (NETs) frequently metastasize to the liver, but it is rare to find them there as primary tumors. Isolated polycystic liver disease (PCLD) is a rare autosomal dominant disease. There is no known association between polycystic liver disease and neuroendocrine or other tumors. We report a case of a 64-year-old female with a past medical history of isolated PCLD who presented ...

Journal: :The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi 2006
Kyung Jin Kim Hyung Joon Yim Min Jeong Kim Rok Son Choung Jong Eun Yeon Hong Sik Lee Kwan Soo Byun Sang Woo Lee Jai Hyun Choi Ho Sang Ryu Chang Hong Lee Jin Hai Hyun Eung Suk Lee Young Sik Kim

Small cell neuroendocrine carcinoma is a type of undifferentiated, malignant neuroendocrine tumor. Most of neuroendocrine tumors exhibit well-differentiated features and are classified as carcinoid tumors. However, carcinomas of the liver with anaplastic characters, which are classified as small-cell carcinomas are extremely rare and only few cases have been reported in the literature. We repor...

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