Results 51 to 60 of about 94,680 (364)

Late recurrence of adrenocortical carcinoma and metastatic disease. Case report

open access: yesRevista de la Facultad de Medicina, 2019
Introduction: Adrenocortical carcinoma (ACC) is a malignancy with an annual incidence of 0.72 cases per million people. It is a rare tumor that is associated with high mortality in late stages, as well as with a 5-year survival of 13% in stage IV ...
Maria Alejandra Pérez-Ardila   +4 more
doaj   +1 more source

Management of adreno-cortical adenomas using microwave ablation: study of the effects of the fat tissue

open access: yesInternational Journal of Hyperthermia, 2022
Background and objectives Adrenocortical neoplasms are the main causes of secondary hypertension and related comorbidities including hypokalemia and cardiovascular diseases.
Anna Bottiglieri   +3 more
doaj   +1 more source

Adrenal lipoma: A case report and literature review

open access: yesUrology Case Reports, 2021
The study reports a case of a 57-year-old female patient with incidental right adrenal lipoma (LA). The tumor was detected by ultrasound (US) and confirmed by computed tomography (CT).Due to the size of the mass, it was decided to perform a laparoscopic ...
Daniel Cereijo Tejedor   +5 more
doaj  

Incidental Finding of Adrenal Oncocytoma After Right Robotic Adrenalectomy: Case Report and Literature Review

open access: yesUrology Case Reports, 2017
Oncocytic neoplasms occur in several organs and are most commonly found in the thyroid, kidneys and salivary glands. Oncocytic neoplasms of the adrenal cortex are extremely rare and are usually non-functioning, benign and incidentally detected.
Othman Alamoudi   +3 more
doaj   +1 more source

Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour

open access: yesThe Egyptian Journal of Internal Medicine, 2014
Oncocytic neoplasms are well recognized in organs such as the kidney, thyroid and salivary glands. They are seen rarely in other sites such as the adrenal cortex.
Abhishek Singhai, Subodh Banzal
doaj   +1 more source

Clonal Composition of Human Adrenocortical Neoplasms [PDF]

open access: yes, 1994
The mechanisms of tumorigenesis of adrenocortical neoplasms are still not understood. Tumor formation may be the result of spontaneous transformation of adrenocortical cells by somatic mutations.
Abdelhamid, S.   +7 more
core  

Large-scale analysis of disease pathways in the human interactome

open access: yes, 2017
Discovering disease pathways, which can be defined as sets of proteins associated with a given disease, is an important problem that has the potential to provide clinically actionable insights for disease diagnosis, prognosis, and treatment ...
Agrawal, Monica   +2 more
core   +1 more source

Post-Partum Pituitary Insufficiency and Livedo Reticularis Presenting a Diagnostic Challenge in a Resource Limited Setting in Tanzania: A Case Report, Clinical Discussion and Brief Review of Existing Literature. [PDF]

open access: yes, 2012
Pituitary disorders following pregnancy are an important yet under reported clinical entity in the developing world. Conversely, post partum panhypopituitarism has a more devastating impact on women in such settings due to high fertility rates, poor ...
A Cénac   +27 more
core   +3 more sources

Simultaneous inhibition of TRIM24 and TRIM28 sensitises prostate cancer cells to antiandrogen therapy, decreasing VEGF signalling and angiogenesis

open access: yesMolecular Oncology, EarlyView.
TRIM24 and TRIM28 are androgen receptor (AR) coregulators which exhibit increased expression with cancer progression. Both TRIM24 and TRIM28 combine to influence the response of castrate‐resistant prostate cancer (CRPC) cells to AR inhibitors by mediating AR signalling, regulation of MYC and upregulating VEGF to promote angiogenesis. Castrate‐resistant
Damien A. Leach   +8 more
wiley   +1 more source

Pheochromocytoma of the organ of Zuckerkandl

open access: yesRadiology Case Reports, 2021
Paragangliomas are uncommon neuroendocrine neoplasms that occur in characteristic locations. While parasympathetic paragangliomas are mainly located at the head and neck, sympathetic paragangliomas are mostly located below the neck. Among parasympathetic
Hoang Di Thu Le, MD   +4 more
doaj  

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