Zobrazeno 1 - 10
of 974
pro vyhledávání: '"Pituitary Carcinoma"'
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionPituitary carcinoma (PC) is an extremely rare tumor of the adenohypophysis, which manifests as craniospinal dissemination and/or systemic metastasis. The diagnosis of PC is particularly difficult, as the clinical diagnosis only can be mad
Externí odkaz:
https://doaj.org/article/551c29d63ad446f9a5824324feef1b0e
Autor:
Ian J. Robertson, Timothy A. Gregory, Steven G. Waguespack, Marta Penas-Prado, Nazanin K. Majd
Publikováno v:
Journal of Immunotherapy and Precision Oncology, Vol 6, Iss 2, Pp 74-83 (2023)
Pituitary carcinoma (PC) is a rare, aggressive malignancy that comprises 0.1–0.2% of all pituitary tumors. PC is defined anatomically as a pituitary tumor that metastasizes outside the primary intrasellar location as noncontiguous lesions in the ce
Externí odkaz:
https://doaj.org/article/da480b6d5bfb44beb5603c976142fb8a
Autor:
Yi Zhang, Victoria Li, Jifang Liu, Huijuan Zhu, Lin Lu, Hui Pan, Renzhi Wang, Kan Deng, Yong Yao
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Metastatic PitNETs are a rare life-threatening condition with poor prognosis and documentation. Due to the scarce literature and lack of precise treatment, we hope to better characterise PitNET using the next-generation whole exon sequencing (WES) an
Externí odkaz:
https://doaj.org/article/f17ad2d3a0174205ac2dc731693daaa0
Autor:
Cristina Lamas, Rosa Cámara, Carmen Fajardo, Pablo Remon-Ruiz, Betina Biagetti, Fernando Guerrero-Pérez, Marta Araujo-Castro, Mireia Mora, Felicia Hanzu, Pedro Iglesias, Rogelio García-Centeno, Alfonso Soto
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Current guidelines recommend temozolomide as the first-line chemotherapy for aggressive pituitary neuroendocrine tumours. However, no clinical trials have been conducted to date and clinical experience is quite limited. We retrospectively analyzed 28
Externí odkaz:
https://doaj.org/article/c995058bd7b74b7e97419ae904fce76f
Akademický článek
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Publikováno v:
Caspian Journal of Internal Medicine, Vol 12, Iss Supplement 2, Pp 467-470 (2021)
Background: It is believed that pituitary carcinoma is a rare disorder and arise from the transformation of benign invasive macroadenomas, and the process of this transformation takes place slowly. Case Presentation: A 51-year-old man presented with
Externí odkaz:
https://doaj.org/article/861847f48a6f4b3a96f3b20e21841efd
Autor:
Stephanie Du Four, Jorn Van Der Veken, Johnny Duerinck, Elle Vermeulen, Corina E. Andreescu, Michael Bruneau, Bart Neyns, Van Velthoven, Brigitte Velkeniers
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Although pituitary adenomas (PAs) account for 15% of intracranial tumors, pituitary carcinomas (PCs) are a rare entity. Most commonly, PCs evolve from aggressive PAs invading the surrounding structures and eventually leading to metastatic lesions. Du
Externí odkaz:
https://doaj.org/article/fe4f5fc21ca5450e8aafab916cec6aa0
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Pituitary carcinoma (PC) is extremely rare, with its incidence only accounting for 0.1%-0.2% of pituitary tumor (PT). Existing histological features, including invasiveness, cellular pleomorphism, nuclear atypia, mitosis, necrosis, etc., can be obser
Externí odkaz:
https://doaj.org/article/674703fd232d4877a1873fa22e275928
Autor:
Elise R. Venable, Sarah E. Kerr, M. Beatriz S. Lopes, Karra A. Jones, Andrew M. Bellizzi, Taofic Mounajjed, Aditya Raghunathan, Oksana Hamidi, Thorvardur R. Halfdanarson, Mabel Ryder, Rondell P. Graham
Publikováno v:
Diagnostic Pathology, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background Pathologists frequently encounter neuroendocrine tumors (NETs) presenting as multiple liver masses in routine practice. Most often, these are well-differentiated tumors with characteristic histologic features. In contrast, pituita
Externí odkaz:
https://doaj.org/article/6763d164554d484295728dbca621424e
Akademický článek
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