Results 91 to 100 of about 539,143 (189)
, 2002 PubMedID: 11922210We report a case of an atypical bronchial carcinoid showing sestamibi uptake. A 27-year-old man with Kallmann's syndrome and hyperparathyroidism had parathyroid scintigraphy with 99mTc-sestamibi. A focal uptake was observed on the right
Kibar M. +5 more
core +1 more source
Neuroendocrine tumours through an epigenetic lens: Emerging insights for diagnosis and treatment
Journal of Neuroendocrinology, Volume 38, Issue 6, June 2026.Abstract Neuroendocrine tumours (NETs) are well‐differentiated epithelial neuroendocrine neoplasms that frequently develop in the small intestine, pancreas, and lungs. NETs originate from neuroendocrine cells specialized in hormone secretion implicated in a number of physiological processes.
Victoria Jacquot +4 more
wiley +1 more source
Nasal atypical carcinoid tumor. A case report [PDF]
, 2016 Introduction: Carcinoid tumors are neuroendocrine tumors that are usually located on the gastrointestinal system, but infrequent in the sinus area. Description: The case of a 55-year-old woman with a unilateral nasal mass is described.
Santos Gorjón, Pablo +4 more
core
CT and MRI findings of thymic carcinoid [PDF]
, 2017 Objective: To evaluate the CT and MRI findings of thymic carcinoid and to compare these findings with previously published findings of thymoma. Methods: 11 cases of pathologically proven thymic carcinoid were reviewed retrospectively.
Shigematsu, Kazuto +12 more
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A Case of Multicentric Carcinoid in a Patient with Psoriatic Spondyloarthropathy
Case Reports in Rheumatology, 2015 We describe the first case of a patient presenting with multicentric carcinoid occurring in the lung and subsequently in the rectum, with chronic psoriatic arthritis.
Nabil George +3 more
doaj +1 more source
Bulletin of the National Research Centre, 2019 Background Carcinoids at atypical sites are rare and mostly asymptomatic. In the majority, they show normal levels of serotonin and its metabolites in plasma and urine, resulting in a relatively late diagnosis and hence guarded prognosis.
Karim G. Moustafa, Gamal M. Saied
doaj +1 more source
Molecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley +1 more source
BMC Cancer, 2018 Background Everolimus was recently approved for the treatment of neuroendocrine tumors. However, its efficacy and tolerability in hemodialysis patients with end-stage renal disease is not established.
M. P. Brizzi +5 more
doaj +1 more source
Atelectasis in pediatrics: a case of carcinoid tumor
Rare Tumors, 2017 Carcinoid pulmonary tumors occur in the fourth to sixth decades of life. Usually, typical carcinoid arise a decade earlier when compared to atypical carcinoid (45 years and 55 years, respectively).
Cláudia Guerreiro +4 more
doaj +1 more source
Primary neuroendocrine carcinoma of thymus: A rare cause of Cushing′s syndrome
Indian Journal of Pathology and Microbiology, 2010 Thymomas constitute majority of the thymic neoplasms. In contrast, neuroendocrine tumors (carcinoid and neuroendocrine carcinoma) of thymus are extremely rare.
Arora Raman +3 more
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