Zobrazeno 1 - 10
of 379
pro vyhledávání: '"PitNET"'
Autor:
T. Elise Potthoff, Carolin Walter, Daniela Jeising, Daniel Münter, Archana Verma, Eric Suero Molina, Walter Stummer, Martin Dugas, Wolfgang Hartmann, Matthias Dottermusch, Lea Altendorf, Ulrich Schüller, Sophia Scheuermann, Christian Seitz, Thomas K. Albert, Kornelius Kerl
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-18 (2024)
Abstract Background Pituitary neuroendocrine tumors (PitNET) are among the most common intracranial tumors. Despite a frequent benign course, aggressive behavior can occur. Tumor behavior is known to be under the influence of the tumor microenvironme
Externí odkaz:
https://doaj.org/article/9d87dc91d88548038291cde05a5e76b8
Autor:
Keiko Taniguchi-Ponciano, Silvia Hinojosa-Alvarez, Jesus Hernandez-Perez, Rocio A. Chavez-Santoscoy, Ilan Remba-Shapiro, Gerardo Guinto, Erika Magallon-Gayon, Benjamin Telles-Ramirez, Rodrigo Ponce de Leon-Conconi, Sandra Vela-Patiño, Sergio Andonegui-Elguera, Amayrani Cano-Zaragoza, Florencia Martinez-Mendoza, Jacobo Kerbel, Marco Loza-Mejia, Juan Rodrigo-Salazar, Alonso Mendez-Perez, Cristina Aguilar-Flores, Antonieta Chavez-Gonzalez, Elenka Ortiz-Reyes, Erick Gomez-Apo, Laura C. Bonifaz, Daniel Marrero-Rodriguez, Moises Mercado
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-20 (2024)
Abstract Pituitary neuroendocrine tumors (PitNET) represent the vast majority of sellar masses. Some behave aggressively, growing rapidly and invading surrounding tissues, with high rates of recurrence and resistance to therapy. Our aim was to establ
Externí odkaz:
https://doaj.org/article/1b6c1939f3f746799fce58209502bf76
Autor:
Ioana Balinisteanu, Lavinia Caba, Andreea Florea, Roxana Popescu, Laura Florea, Maria-Christina Ungureanu, Letitia Leustean, Eusebiu Vlad Gorduza, Cristina Preda
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 8, Pp 9093-9121 (2024)
Acromegaly is a rare endocrine disorder characterized by the excessive production of growth hormone (GH) in adulthood. Currently, it is understood that certain pituitary neuroendocrine tumors (PitNETs) exhibit a hereditary predisposition. These tumor
Externí odkaz:
https://doaj.org/article/b53c9e28ccd7456c81452098d88c379b
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Pituitary neuroendocrine tumors are common, typically benign intracranial neoplasms arising from well-differentiated anterior pituitary cells with prevalence of clinically relevant pituitary tumor of 89 in 100 000 people. Despite the growing number o
Externí odkaz:
https://doaj.org/article/4daf3cde1f2d4c09b832d88e29a4c484
Autor:
Jakub Skiba, Zuzanna Skiba, Kinga Tylczyńska, Natalia Tylczyńska, Kinga Kowalik, Maria Michalska, Aleksandra Zielińska, Szymon Szypulski, Sebastian Iwaniuk, Ignacy Maciejewski
Publikováno v:
Quality in Sport, Vol 33 (2024)
Introduction and Purpose: Pituitary neuroendocrine tumors (PitNETs), commonly known as pituitary adenomas, are tumors originating from the adenohypophysis. The purpose of this review was to provide a comprehensive overview of the latest classificatio
Externí odkaz:
https://doaj.org/article/ccdd9cad8d3e48c8ab0a30b775cc8ae5
Autor:
Kosaku AMANO, Yuichi ODA, Yasufumi SEKI, Kaoru YAMASHITA, Kanako BOKUDA, Atsuhiro ICHIHARA, Takakazu KAWAMATA
Publikováno v:
Neurologia Medico-Chirurgica, Vol 64, Iss 4, Pp 160-167 (2024)
Prolactin-producing pituitary tumor (PRLoma) is the most prevalent functional pituitary tumor. If the tumor becomes large, vision can be impaired. In contrast to other pituitary tumors, cabergoline (CAB) is extremely effective for PRLoma and has beco
Externí odkaz:
https://doaj.org/article/bdcdb58284744ebf9025d79830cf2b11
Autor:
Chariene Shao-Lin Woo, Ronnie Siu-Lun Ho, Grace Ho, Hoi-To Lau, Carol Ho-Yi Fong, Johnny Yau-Cheung Chang, Eunice Ka-Hong Leung, Lawrence Chi-Kin Tang, Ivan Kwok-Ming Ma, Alan Chun-Hong Lee, David Tak-Wai Lui, Yu-Cho Woo, Wing-Sun Chow, Gilberto Ka-Kit Leung, Kathryn Choon-Beng Tan, Karen Siu-Ling Lam, Chi-Ho Lee
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundThe 2022 World Health Organization (WHO) classification of pituitary neuroendocrine tumour (PitNET) supersedes the previous one in 2017 and further consolidates the role of transcription factors (TF) in the diagnosis of PitNET. Here, we inv
Externí odkaz:
https://doaj.org/article/56b745f0e9cc4d55bed42a486d209ba7
Autor:
Yukiko Usui, MD, Ryo Kurokawa, MD, PhD, Takahiro Fukushima, MD, Richi Fujita, MD, Reina Hosoi, MD, Emi Miyawaki, MD, Michio Hayashi, MD, Sadahiro Kishisita, MD, Mariko Kurokawa, MD, Osamu Abe, MD, PhD, Haruyasu Yamada, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 9, Pp 2943-2947 (2023)
Ectopic pituitary neuroendocrine tumors (PitNETs) are uncommon conditions that develop outside of the sella turcica. The sphenoid sinus is the most common site for ectopic PitNET, followed by the suprasellar region, clivus, and cavernous sinus. PitNE
Externí odkaz:
https://doaj.org/article/e7a3ce66459f4b068a0e935958885959
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Autor:
Monika Pękul, Magdalena Szczepaniak, Paulina Kober, Natalia Rusetska, Beata J. Mossakowska, Szymon Baluszek, Artur Kowalik, Maria Maksymowicz, Grzegorz Zieliński, Jacek Kunicki, Przemysław Witek, Mateusz Bujko
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionCorticotroph pituitary neuroendocrine tumors (PitNETs) develop from ACTH-producing cells. They commonly cause Cushing’s disease (CD), however, some remain clinically silent. Recurrent USP8, USP48, BRAF and TP53 mutations occur in cortic
Externí odkaz:
https://doaj.org/article/3f226b8e125942638449b20825719fce