Results 121 to 130 of about 1,396,034 (289)

Past, Present and Future of Epigenetics in Adrenocortical Carcinoma

open access: yesCancers, 2020
DNA methylation profiling has been suggested a reliable technique to distinguish between benign and malignant adrenocortical tumors, a process which with current diagnostic methods remains challenging and lacks diagnostic accuracy of borderline tumors ...
M. Ettaieb   +3 more
semanticscholar   +1 more source

Mosaic Li Fraumeni Syndrome Not Identified in Germinal Tissue

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 2, February 2026.
In this study, we presented the first clinical case report of mosaic Li Fraumeni syndrome eluding germinal tissue. This case highlights the complexity of interpreting mosaic variants in TP53, and the difficulty in relaying cancer and reproductive risk information in the context of mosaic Li Fraumeni syndrome.
Rhianna M. Urban   +9 more
wiley   +1 more source

Nonfunctioning adrenocortical carcinoma: a study of 12 cases

open access: yesJournal of Pathology of Nepal, 2012
Background: Adrenal cortical carcinoma is a rare malignant tumor. Several systems were proposed for diagnosis and evaluation of adrenocortical tumors.Weiss system is most commonly used method for assessment of malignancy, but only few studies has applied
S Ghanghoria   +3 more
doaj   +1 more source

Adrenal insufficiency due to bilateral adrenal metastases - A systematic review and meta-analysis [PDF]

open access: yes, 2019
Objective: Bilateral adrenal metastases may cause adrenal insufficiency (AI) but it is unclear if screening for AI in patients with bilateral adrenal metastases is justified, despite the potential for adrenal crises. Method: A search using PubMed/Medline,
Falhammar, Henrik   +3 more
core   +1 more source

Adjuvant Radiation Improves Recurrence-Free Survival and Overall Survival in Adrenocortical Carcinoma.

open access: yesJournal of Clinical Endocrinology and Metabolism, 2019
CONTEXT Adrenocortical carcinoma (ACC) is a rare malignancy with high rates of recurrence and poor prognosis. The role of radiotherapy (RT) in localized ACC has been controversial and is not routinely offered.
L. Gharzai   +13 more
semanticscholar   +1 more source

Pneumoperitoneum in two cats treated with trilostane for hypercortisolism

open access: yesVeterinary Record Case Reports, Volume 14, Issue 1, February 2026.
Abstract This report describes two cases of pneumoperitoneum in cats receiving treatment for hypercortisolism and diabetes mellitus. Both cats presented with abdominal distention and lethargy and diagnoses of pneumoperitoneum were radiographically confirmed.
Nicholas James Kelly   +4 more
wiley   +1 more source

Molecular Drivers of Potential Immunotherapy Failure in Adrenocortical Carcinoma

open access: yesJournal of Oncology, 2019
Adrenocortical carcinoma (ACC) is a rare, highly aggressive cancer, often insensitive to conventional chemotherapeutics agents. Early diagnosis, followed by radical surgical resection plus/minus adjuvant mitotane therapy, is nowadays the only valuable ...
C. Fiorentini   +6 more
semanticscholar   +1 more source

Clinical significance and immune microenvironment association of cuproptosis‐related genes in pan‐cancer

open access: yesExperimental Physiology, Volume 111, Issue 2, Page 539-555, 1 February 2026.
Abstract Recent studies highlight the important roles of cuproptosis in cancer cells. However, the roles of the cuproptosis‐related genes (CRGs) in different cancers are still not fully understood. Comprehensive analysis was performed using open‐source bioinformatic platforms to disclose the expression profiles, prognostic significance, genomic and ...
Xinyu Ge   +10 more
wiley   +1 more source

Clinical results of the use of mitotane for adrenocortical carcinoma

open access: yesBrazilian Journal of Medical and Biological Research, 2000
Mitotane (o,p'-DDD) acts mainly as an inhibitor of intramitochondrial pregnenolone and cortisol synthesis. Its adrenolytic effect depends on metabolic activation due to conversion to o,p'-DDA and o,p'-DDE.
A.A. Kasperlik-Zaluska
doaj   +1 more source

Adrenal pheochromocytoma incidentally discovered in a patient with parkinsonism [PDF]

open access: yes, 2015
To evaluate the diagnostic route of pheochromocytoma (PHEO) in a patient under dopaminergic treatment. A 70-year-old man with Parkinsonism and under treatment with levodopa and carbidopa came to our observation for evaluation of arterial hypertension and
Claudio Letizia   +7 more
core   +1 more source

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