Results 51 to 60 of about 118,423 (273)

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

International Journal of Dermatology, EarlyView.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla, Zseraldin Metyovinyi, Fanni Adél Meznerics, Arash Mirzahosseini, Judit Tőke, Miklós Tóth, Henriett Butz, Attila Patócs, Márta Medvecz   +8 more
wiley   +1 more source

Systematic review reveals lack of quality in reporting health-related quality of life in patients with gastroenteropancreatic neuroendocrine tumours [PDF]

, 2016
Overview on primary outcomes and HRQoL results of studies included in systematic review.
Barbara Sperner-Unterweger, Bernhard Holzner, Bernhard Nilica, Caroline Martini, Eva-Maria Gamper, Irene Virgolini, Lisa Wintner   +6 more
core   +2 more sources

Carcinoid Tumor of the Cecal Appendix [PDF]

, 2022
Oscar A Salirrosas Roncal, Christian Tantalean Gutierrez, Cesar Llerena Vasquez   +2 more
openalex   +1 more source

Recommendations for bone‐directed therapy in patients with neuroendocrine tumour skeletal metastases at the New Zealand National Neuroendocrine Tumour Multidisciplinary Meeting

Internal Medicine Journal, EarlyView.
Abstract The role of anti‐resorptive agents in patients with bone metastases from neuroendocrine neoplasms is unclear. Our aim was to review bone‐specific treatment recommendations by the New Zealand National Neuroendocrine Tumour Multidisciplinary Meeting (MDM).
Gayle Radley, Marianne S Elston, Ben Lawrence, Veronica Boyle   +3 more
wiley   +1 more source

Minute ampullary carcinoid tumor with lymph node metastases: a case report and review of literature

World Journal of Surgical Oncology, 2009
Background Carcinoid tumors are usually considered to have a low degree of malignancy and show slow progression. One of the factors indicating the malignancy of these tumors is their size, and small ampullary carcinoid tumors have been sometimes treated ...
Sakano Shigeru, Okutani Toshio, Ashida Cho, Higashida Akihiro, Ohnishi Katsuhiro, Fujimoto Koji, Senda Eri, Yamamoto Masayuki, Ito Rieko, Yamada Hajime   +9 more
doaj   +1 more source

Incidence patterns and temporal trends of childhood cancer in Germany, 1980–2019: Forty years of childhood cancer registration in Germany

International Journal of Cancer, Volume 158, Issue 6, Page 1541-1554, 15 March 2026.
What's new? Childhood cancer ranks among the leading causes of disease‐related deaths in children in high‐income countries. Established risk factors, however, account for only a small proportion of incident childhood cancers. In this report, the authors present the first long‐term assessment of temporal trends in childhood cancer incidence rates in ...
Friederike Erdmann, Maike Wellbrock, Claudia Trübenbach, Desiree Grabow, Martin Schrappe, Peter Kaatsch, Claudia Spix, Joachim Schüz, Cécile M. Ronckers   +8 more
wiley   +1 more source

Evaluation of demographic and rare clinical characteristics of patients with thoracic carcinoid tumor in Razi and Aria Hospitals of Rasht during 2006-2016

Journal of Family Medicine and Primary Care, 2022
Introduction: Carcinoid tumors are malignant neoplasms of neuroendocrine cells. This study tended to evaluate the demographic and rare clinical characteristics of patients with thoracic carcinoid tumor during 2006-2016 at Razi and Aria Hospitals in Rasht.
Manouchehr Aghajanzadeh, Mohammad Reza Asgary, Ali Alavi Fomani, Alireza Jafarinegad, Azita Tangestaninejad, Hossein Hosseinzadeh Asli, Maryam Ahmad Khan beige, Rastin Hosseinzadeh Asli, Mohammad Madi Asgari   +8 more
doaj   +1 more source

Novel therapeutic strategy targeting STMN1 using chlorambucil‐conjugated pyrrole–imidazole polyamide in small cell lung cancer

International Journal of Cancer, Volume 158, Issue 5, Page 1336-1347, 1 March 2026.
What's New? Small cell lung cancer (SCLC) is aggressive and difficult to treat but exhibits high levels of stathmin 1 (STMN1), a candidate therapeutic target. In this study, the authors synthesized a chlorambucil (Chb)‐conjugated pyrrole–imidazole polyamide (PIP) compound targeting the STMN1 promoter and DNA sequences and evaluated its efficacy in ...
Ryohei Yoshikawa, Takayoshi Watanabe, Yoichi Ohtaki, Toshikazu Bando, Hiroshi Sugiyama, Takuya Araki, Hideaki Yashima, Bilguun Erkhem‐Ochir, Haruka Okami, Gendensuren Dorjkhorloo, Ikuma Shioi, Toshiteru Nagashima, Natsuko Kawatani, Tomohiro Yazawa, Eiji Narusawa, Takayuki Kosaka, Osamu Kawashima, Mitsuhiro Kamiyoshihara, John D. Minna, Luc Girard, Ken Shirabe, Hiroki Nagase, Kimihiro Shimizu, Takehiko Yokobori   +23 more
wiley   +1 more source

Rare Case of Neuroendocrine Metastasis to the Left Ventricle

JACC: Case Reports
Carcinoid syndrome is a constellation of signs and symptoms caused by different hormones produced by carcinoid tumors. Very rarely, those tumors can metastasize to the heart and cause cardiac involvement of the tumor. This study presents a very rare case
Said Hajouli, MD, Jacob A. Misenheimer, MD, Amir Kamran, MD, Kerry Drabish, PhD, APRN, FNP-BC, Frank H. Annie, PhD, MPA, Fahad F. Bafakih, MD, Yodsui F. Hernandez, MD, Ahmad Elashery, MD   +7 more
doaj   +1 more source

Constipation, the sole presentation of primary renal carcinoid tumor: A case report

Rare Tumors, 2019
Primary renal carcinoid tumors are quite rare. The pathogenesis of these tumors is unknown due to lack of enterochromaffin cells in the kidney. Because of nonspecific clinical manifestations and radiologic features, they are commonly misdiagnosed. Hence,
Mehdi Salehipour, Amir Ahmad Mostaghni, Bita Geramizadeh, Alireza Makarem, Alireza Rezvani   +4 more
doaj   +1 more source