Results 251 to 260 of about 1,718,006 (300)
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Pancreatic neuroendocrine tumors

Disease-a-Month, 2013
Pancreatic neuroendocrine tumors (PNETs) have an incidence of approximately 1 per 100,000 individuals per year, and account for 1–2% of all pancreatic tumors. The annual incidence in the United States is about 3.65 per 100,000 population. Although they may manifest at any age, they most often occur in the fourth to sixth decades of life. Most PNETs are
Thiruvengadam, Muniraj   +4 more
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Pancreatic tumors in children

Pediatric Surgery International, 1996
Pancreatic tumors rarely present in childhood. Diagnostic difficulty and inappropriate treatment may occur due to the variable clinical appearance of the illness. A 26-year audit (1968-1994) at this institution showed five patients ranging in age from 5 to 14 years who were operated upon for pancreatic tumors, four of which were malignant. In two cases
J, Grochowski   +3 more
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Pancreatic Endocrine Tumors

Pathology - Research and Practice, 1988
In this review the current state of our understanding of endocrine tumors of the pancreas is considered. It is based on the experience with a series of 365 tumors. The first part of the article focuses on origin and classification, markers, frequency, criteria of malignancy as well as general structural features of the pancreatic endocrine tumors.
G, Klöppel, P U, Heitz
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Pancreatic endocrine tumors

Current Opinion in Oncology, 2001
Pancreatic endocrine tumors are rare but have long held a fascination for clinicians because of the physiologic derangements that they can cause, and the dramatic corrections that can be achieved by appropriate management. In the year reviewed in this article, the literature again demonstrated the ongoing interest and research in this area.
J, Chun, G M, Doherty
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Rare pancreatic tumors

Abdominal Radiology, 2017
In this review, we will focus on rare pancreatic tumors. Most of these tumors do not have distinct characteristic appearances so the key to diagnosis requires a combination of imaging appearance, laboratory data, patient demographics, and associated medical syndromes in order to narrow the differential diagnosis. Nonetheless, imaging plays a vital role
Jonathan, Steinman   +4 more
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Pancreatic Endocrine Tumors

Gastroenterology Clinics of North America, 2007
Incidental, nonfunctional pancreatic endocrine tumors (PET) are observed with increasing frequency. Most are insulinomas. Endoscopic ultrasound with fine-needle aspiration plays a significant role in the localization and tissue diagnosis of PET. Establishing PET behavior as aggressive or indolent remains challenging especially preoperatively.
Niraj, Jani   +2 more
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Benign Pancreatic Tumors

Surgical Clinics of North America, 2007
The goal of this article is to describe the different types of benign pancreatic neoplasms, methods to distinguish between them, and treatment options. Pancreatic adenocarcinoma is associated with specific neoplastic lesions that are similar in radiographic appearance to some benign lesions.
Sushanth, Reddy, Christopher L, Wolfgang
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Pancreatic Tumor Microenvironment

2020
The pancreatic ductal adenocarcinoma (PDAC) microenvironment is a diverse and complex milieu of immune, stromal, and tumor cells and is characterized by a dense stroma, which mediates the interaction between the tumor and the immune system within the tumor microenvironment (TME).
Kai, Wang, Hong, He
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Pancreatic neuroendocrine tumors

Indian Journal of Gastroenterology, 2012
Pancreatic neuroendocrine tumors (pancreatic NETs) are rare, low- to intermediate-grade neoplasms thought to arise from the pancreatic islets. Recent advances in pathology and our understanding of the biological behavior of this group of tumors has resulted in changes in their nomenclature and how we treat them.
Shailesh V, Shrikhande   +3 more
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Pancreatic Endocrine Tumors

Seminars in Oncology, 2010
Pancreatic endocrine tumors have been steadily growing in incidence and prevalence during the last two decades, showing an incidence of 4-5/1,000,000 population. They represent a heterogeneous group with very varying tumor biology and prognosis. About half of the patients present clinical symptoms and syndromes related to substances released from the ...
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