Results 111 to 120 of about 4,267,390 (291)
Primary malignant tumors of the adrenal glands
Clinics, 2018 Malignancy must be considered in the management of adrenal lesions, including those incidentally identified on imaging studies. Adrenocortical carcinomas (ACCs) are rare tumors with an estimated annual incidence of 0.7–2 cases per year and a worldwide ...
M. Almeida +4 more
semanticscholar +1 more source
Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc [PDF]
, 2008 Context: Mitochondrial cytochrome P450scc converts cholesterol to pregnenolone in all steroidogenic tissues. Although progesterone production from the fetally-derived placenta is necessary to maintain pregnancy to term, four patients with mutations in ...
Huang, NW +6 more
core
International Journal of Cancer, EarlyView.ABSTRACT Adjuvant nivolumab is approved for esophageal or gastroesophageal junction cancer after neoadjuvant chemoradiotherapy and resection. In the CheckMate‐577 trial, Grade 3–5 nivolumab‐related adverse events (AEs) occurred in 5% of patients, with early discontinuation due to toxicity in 9%. However, real‐world data on immunotherapy‐related adverse
Michelle Koops van ’t Jagt +7 more
wiley +1 more source
Adrenal tumors. Literature review
Acta Médica del Centro, 2014 Tumors of adrenal origin may be derived from the cortex or the medulla, which depends on the type of functionality that can be developed. Adrenal masses have varying styles.
Vivian de la Caridad Betancourt Rodríguez +1 more
doaj
Case report: Imaging of adrenal adenomatoid tumors: reports of two cases and review of literature
Frontiers in OncologyAdenomatoid tumors (ATs) are uncommon, benign tumors of mesothelial origin, most frequently found in the genital tracts of both sexes. Extragenital localization sites, such as adrenal glands, are extremely rare.
Yuanyuan Wu +7 more
doaj +1 more source
Frontiers in Endocrinology, 2015 Adrenocortical tumors (ACT) in children are very rare and are most frequently diagnosed in the context of the Li-Fraumeni syndrome, a multiple cancer syndrome linked to germline mutations of the tumor suppressor gene TP53 with loss of heterozygosity in ...
E. Lalli, B. Figueiredo
semanticscholar +1 more source
Adrenal Myelolipoma: A Case Presentation [PDF]
, 2018 Adrenal myelolipomas are non-functional benign tumors of hematopoietic and mature adipose tissue. Adrenal myelolipomas, which are generally detected in post-mortem examinations, have become more detectable thanks to evolution and frequent use of imaging ...
Ayhan Dirim +7 more
core +1 more source
Familial Cancers Associated With Cancers of the Breast, Prostate, Colorectum, and Lung in Sweden
International Journal of Cancer, EarlyView.ABSTRACT Available epidemiological evidence shows that many cancers share familial risks, and this is increasingly confirmed by data on shared pathogenic germline gene variants between cancers. We decided to harness the world's largest resource on familial cancer to assess discordant familial risks for female breast (BC), prostate (PC), colorectal (CRC)
Frantisek Zitricky +5 more
wiley +1 more source
Expressions of LncRNA HOTAIR and VEGF in adrenal malignant tumors and their prognostic significance
Linchuang shenzangbing zazhi, 2021 Objective To explore the expression levels of long non-coding RNAHOX transcript antisense intergenic RNA（LncRNAHOTAIR）and vascular endothelial growth factor（VEGF）in patients with adrenal malignant tumor,and analyze their prognostic relationship.Methods ...
Du Xue-qian +2 more
doaj
Journal of Clinical Endocrinology and Metabolism, 2017 Context: Patients with 21-hydroxylase deficiency (21OHD) have long-term complications, resulting from poor disease control and/or glucocorticoid overtreatment.
Adina F. Turcu +8 more
semanticscholar +1 more source