Zobrazeno 1 - 10
of 1 425
pro vyhledávání: '"Endocrine tumor"'
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Externí odkaz:
https://doaj.org/article/f3f9364230c044e98b71d1d5af2f4038
Multidisciplinary management of difficult/aggressive growth-hormone pituitary neuro-endocrine tumors
Autor:
Antonio Bianchi, Sabrina Chiloiro, Antonella Giampietro, Simona Gaudino, Rosalinda Calandrelli, Ciro Mazzarella, Carmelo Caldarella, Mario Rigante, Marco Gessi, Liverana Lauretti, Laura De Marinis, Alessandro Olivi, Alfredo Pontecorvi, Francesco Doglietto
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Growth Hormone-secreting adenomas exhibits variable biological behavior and heterogeneous natural history, ranging from small adenomas and mild disease, to invasive and aggressive neoplasms with more severe clinical picture. Patients not cured or con
Externí odkaz:
https://doaj.org/article/acd8af224cfc4bf6ac79dff396754844
Autor:
Mihai Cristian Dumitrascu, Diana Elena Rentea, Eugenia Petrova, Adina Draghici, Adina Ghemigian, Mara Carsote, Anda Dumitrascu, Claudia Mehedintu, Florica Sandru
Publikováno v:
Romanian Medical Journal, Vol 68, Iss 4, Pp 525-529 (2021)
Hemoptysis as first sign of a thyroid differentiated cancer represents an atypical behavior of a cervical mass, usually associating lung metastasis or direct tracheal invasion. Late presentation (for instance, due to COVID-19 pandemic circumstances)
Externí odkaz:
https://doaj.org/article/be8aca83472a4f73a8b3a37ee3ee8e66
Publikováno v:
Urology Case Reports, Vol 44, Iss , Pp 102170- (2022)
Paraganglioma (PGL) of the urinary bladder are a very rare tumor entity. Treatment of a PGL requires a multidisciplinary approach. We report on a case of a malignant pheochromocytoma (PHEO) of the bladder in a male adult due to a succinate dehydrogen
Externí odkaz:
https://doaj.org/article/eff8245ef43e48d792b08b1d93facd52
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/f7829a2bc4334292a8c855433da9caa0
Autor:
Catherine Cardot Bauters, Emmanuelle Leteurtre, Bruno Carnaille, Christine Do Cao, Stéphanie Espiard, Malo Penven, Evelyne Destailleur, Isabelle Szuster, Tonio Lovecchio, Julie Leclerc, Fredéric Frénois, Emmanuel Esquivel, Patricia L M Dahia, Emilie Ait-Yahya, Michel Crépin, Pascal Pigny
Publikováno v:
Endocrine Connections, Vol 9, Iss 10, Pp 1042-1050 (2020)
Objective: We previously described a family in which predisposition to pheochromocytoma (PCC) segregates with a germline heterozygous KIF1B nucleotide variant (c.4442G>A, p.Ser1481Asn) in three generations. During the clinical follow-up, one proband
Externí odkaz:
https://doaj.org/article/ca41063f169c4c678438ac8529d46395
Exploring the role of systemic therapy in adult adrenocortical carcinoma: A single-center experience
Autor:
Akhil Kapoor, Vanita Noronha, Anup Toshniwal, Santosh Menon, Amit Joshi, Vijay M Patil, Nandini Menon, Gagan Prakash, Vedang Murthy, Rahul Krishnatry, Ganesh Bakshi, Mahendra Pal, Palak Popat, Nilesh Sable, Kumar Prabhash
Publikováno v:
Cancer Research, Statistics, and Treatment, Vol 3, Iss 2, Pp 192-200 (2020)
Background: Adrenocortical carcinoma (ACC) is a rare malignancy with poor outcomes. Objectives: To analyze the clinicopathologic features, treatment patterns and outcomes of patients with ACC who received systemic therapy at our center. Patients and
Externí odkaz:
https://doaj.org/article/090a7a9efdd54459b3fe45661011123e
Autor:
Emilie Baron, Catherine Szymanski, Hélène Hergault, Céline Lepère, Olivier Dubourg, Marie Hauguel‐Moreau, Nicolas Mansencal
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 23 (2021)
Background The development of carcinoid heart disease (CaHD) is still relatively unclear. It is difficult to define an optimal follow‐up for patients without any cardiac involvement at baseline. The aim of this study was to assess the prevalence an
Externí odkaz:
https://doaj.org/article/b997bddae3f5426e954e08fd8a38a704
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/608e20ab6e06433f9b6b94315fb2487f
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract Background With increasing treatment options available, neuroendocrine tumor has become a chronic disease and may present later on with atypical manifestation of disease spread once resistant to treatment. Case presentation A 74-year-old whi
Externí odkaz:
https://doaj.org/article/6c2c6bb2e55d4ad7b25e6bd9abe22f45