Zobrazeno 1 - 10
of 14 415
pro vyhledávání: '"neuroendocrine tumor"'
Autor:
Taghreed I. Alshafeiy, Hazwa Karathanathodi Hamza, Reem Al-Mazroui, Badriya Al-Qassabi, Suad Al-Aghbari
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-6 (2024)
Abstract Background Primary breast carcinoma is far more common than breast metastases. Common breast metastases usually come from lymphoma, leukemia, melanoma, and ovarian cancers. Breast metastases from neuroendocrine carcinomas are considered an e
Externí odkaz:
https://doaj.org/article/1016fc01205f4da1a358e7e8a5fbca59
Autor:
Jong-Uk Park, Jae-Hyun Jo, Sangjune Kim, Christophe E. Redon, Mirit I. Aladjem, Yuri Seo, Se Jin Jang, Sang-Min Jang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Neuroendocrine tumor (NET) is a rare malignant tumor, notably small cell lung cancer (SCLC), a type of lung neuroendocrine tumor, which has a survival rate of less than 7%. Although various biomarkers including CHGA (Chromogranin A), INSM1 (
Externí odkaz:
https://doaj.org/article/914d4610c8ac474cb06d2331a2f7b7a5
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Thymic neuroendocrine tumor as a cause of Cushing syndrome is extremely rare in children. Case presentation We report a case of a 10-year-old girl who presented with typical symptoms and signs of hypercortisolemia, including bone
Externí odkaz:
https://doaj.org/article/3fdbe77b3fd1486084cca3584631b063
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:
Heli Gao, Wuhu Zhang, Zheng Li, Wensheng Liu, Mengqi Liu, Qifeng Zhuo, Yihua Shi, Wenyan Xu, Chenjie Zhou, Yi Qin, Jin Xu, Jie Chen, Xianjun Yu, Xiaowu Xu, Shunrong Ji
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capec
Externí odkaz:
https://doaj.org/article/07be9ba86f7a4a8dbe7f208d56ee4cc4
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 52, Iss 3, Pp 178-187 (2024)
Neuroendocrine tumors (NETs) are a heterogeneous group of slowly progressing tumors from neuroendocrine cells able to secrete biologically active substances. The most striking clinical manifestation of functioning NETs is the carcinoid syndrome, whic
Externí odkaz:
https://doaj.org/article/a36490dc36e54ee28a67ee5ed95af492
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Grade 3 neuroendocrine tumor (G3 PanNET) and poorly differentiated neuroendocrine carcinoma (PanNEC) of the pancreas are considered distinct entities from a biological and prognostic perspective but may have overlapping features c
Externí odkaz:
https://doaj.org/article/8104da488e8a45a99cf5c9175dee26e5
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundThyrotropin (TSH)-secreting pituitary neuroendocrine tumors (PitNETs) are recognized as a rare disease. Mixed TSH PitNETs account for 20–25% of TSH PitNETs. This study aimed to report an extremely rare case of a mixed TSH PitNET coexistin
Externí odkaz:
https://doaj.org/article/4daab14755f642b183f607d956f7b9bd
Autor:
Karen N. Rojas, BS, Kanishka Chelikani, BS, Javier Villanueva-Meyer, MD, Peeyush Bhargava, MD, MBA
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5688-5691 (2024)
This case report follows a 63-year-old female patient with a history of a gastroenteropancreatic (GEP) neuroendocrine tumor of the terminal ileum who developed ovarian metastasis and later progressed to peritoneal carcinomatosis. The patient was foun
Externí odkaz:
https://doaj.org/article/eaefc9979bb04fb59ff75fc4dbf192f8
Autor:
Hülya Hacışahinoğulları, Şevkican Güneş, Ümmü Mutlu, Emine Göknur Işık, Yalın İşcan, Nihat Aksakal, Gülşah Yenidünya Yalın, Nurdan Gül, Ayşe Kubat Üzüm, Özlem Soyluk Selçukbiricik
Publikováno v:
İstanbul Medical Journal, Vol 25, Iss 3, Pp 236-240 (2024)
Introduction: Insulinoma is a rare disease, however the most common cause of hypoglycemia due to excess insulin secretion. Diagnosis and localization can be challenging. This study evaluated the clinical features, diagnostic workup, management, and o
Externí odkaz:
https://doaj.org/article/948c996112674246998a726773c63047