Results 211 to 220 of about 99,632 (265)

A 40‐year‐old woman with a spinal mass

Brain Pathology, EarlyView.
Melissa Mejia‐Bautista, Margarita Loxas, Pouya Jamshidi, Drew Duckett, Jean‐Paul Wolinsky, Jared T. Ahrendsen   +5 more
wiley   +1 more source

An Update on Novel Pharmacotherapies for the Treatment of Neuroendocrine Tumors. [PDF]

Int J Mol Sci
Choucair K, Odabashian R, Reddy SN, Azmi AS, Saif MW.   +4 more
europepmc   +1 more source

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Pituitary neuroendocrine tumors: a model for neuroendocrine tumor classification

Modern Pathology, 2021
The classification of adenohypophysial neoplasms as "pituitary neuroendocrine tumors" (PitNETs) was proposed in 2017 to reflect their characteristics as epithelial neuroendocrine neoplasms with a spectrum of clinical behaviors ranging from small indolent lesions to large, locally invasive, unresectable tumors.
Sylvia L. Asa, Ozgur Mete, Michael D. Cusimano, Ian E. McCutcheon, Arie Perry, Shozo Yamada, Hiroshi Nishioka, Olivera Casar-Borota, Silvia Uccella, Stefano La Rosa, Ashley B. Grossman, Shereen Ezzat, null International Pituitary Pathology, Sofia Asioli, Süheyla Uyar Bozkurt, Nil Comunoglu, Giulia Cossu, Peter Earls, Nuperi Gazioglu, Richard A. Hickman, Hidetoshi Ikeda, Emilija Manojlovic-Gacic, Mahmoud Messerer, Buge Öz, Sara Pakbaz, Federico Roncaroli, Wolfgang Saeger, John Turchini, Sema Yarman   +28 more
openaire   +2 more sources

Neuroendocrine Tumors

Gastroenterology Clinics of North America, 2016
Neuroendocrine tumors are increasingly diagnosed, either incidentally as part of screening processes, or for symptoms, which have commonly been mistaken for other disorders initially. The diagnostic workup to characterize tumor behaviour and prognosis focuses on histologic, anatomic, and functional imaging assessments. Several therapeutic options exist
Basuroy, Ron, Srirajaskanthan, Raj, Ramage, John K   +2 more
openaire   +3 more sources

Neuroendocrine tumors of the diffuse neuroendocrine system

Current Opinion in Oncology, 2008
Neuroendocrine tumors (previously referred to as carcinoids) are ill-understood, enigmatic malignancies that, although slow-growing compared with adenocarcinomas, can behave aggressively. In 2004, they comprised 1.25% of all malignancies; their incidence is increasing by approximately 6% per year.
Björn I, Gustafsson, Mark, Kidd, Irvin M, Modlin   +2 more
openaire   +2 more sources

Tumor Markers in Neuroendocrine Tumors

Digestion, 2000
Most neuroendocrine tumors produce and secrete a multitude of peptide hormones and amines. Some of these substances cause a specific clinical syndrome: carcinoid, Zollinger-Ellison, hyperglycemic, glucagonoma and WDHA syndrome. Specific markers for these syndromes are basal and/or stimulated levels of urinary 5-HIAA, serum or plasma gastrin, insulin ...
K, Oberg, E T, Janson, B, Eriksson
openaire   +3 more sources

Neuroendocrine tumor of the rectum

The American Journal of Surgery, 2009
The authors report a case of a neuroendocrine tumor of the rectum. A 57-year-old man was revealed to have a large tumor of the rectum with invasion to the urinary bladder and seminal capsule. After resection, the tumor was revealed to be composed of neuroendocrine cells.
Koichi, Suyama, Naoko, Hayashi, Hironobu, Shigaki, Nobutaka, Sato, Kotaro, Hirashima, Yohei, Nagai, Yukiharu, Hiyoshi, Yasuo, Sakamoto, Naoya, Yoshida, Eiichiro, Toyama, Masayuki, Watanabe, Hideo, Baba   +11 more
openaire   +2 more sources