Results 11 to 20 of about 114,029 (285)
Transradial Embolization of Hemorrhagic Adrenal Myelolipoma
The Arab Journal of Interventional Radiology, 2022 Adrenal myelolipomas are largely benign, non-functioning, and asymptomatic adrenal tumors found incidentally on imaging. These tumors have an extremely low incidence and are exceedingly rare.
Griffin Mcnamara +6 more
doaj +1 more source
Indian Journal of Medical and Paediatric Oncology, 2020 Context: Adrenal tumors can arise either from cortex or from medulla; both the regions being structurally and functionally different. Current knowledge on childhood adrenocortical tumors (ACTs), the management approach, and the outcome is limited due to ...
Prasanta Kumar Tripathy +3 more
doaj +1 more source
Tumors in von Hippel–Lindau Syndrome: From Head to Toe—Comprehensive State-of-the-Art Review [PDF]
, 2018 Von Hippel–Lindau syndrome (VHL) is an autosomal-dominant hereditary tumor disease that arises owing to germline mutations in the VHL gene, located on the short arm of chromosome 3.
Bhalla, Sanjeev +6 more
core +1 more source
Adrenal imaging (Part 2): Medullary and secondary adrenal lesions
Indian Journal of Endocrinology and Metabolism, 2015 Adrenal malignancies can be either primary adrenal tumors or secondary metastases, with metastases representing the most common malignant adrenal lesion.
Ekta Dhamija +3 more
doaj +1 more source
Methylation status of Vitamin D receptor gene promoter in benign and malignant adrenal tumors [PDF]
, 2015 We previously showed a decreased expression of vitamin D receptor (VDR) mRNA/protein in a small group of adrenocortical carcinoma (ACC) tissues, suggesting the loss of a protective role of VDR against malignant cell growth in this cancer type ...
Cappellesso, Rocco +7 more
core +4 more sources
Urology Case Reports, 2022 Testicular adrenal rest tumors are a rare development of patients with congenital adrenal hyperplasia. It is difficult to diagnose due to similarities with Leydig cell tumors. Treatment can be conservative or surgical.
Corey Able +4 more
doaj +1 more source
An exceedingly rare adrenal collision tumor: adrenal adenoma–metastatic breast cancer–myelolipoma
Journal of Community Hospital Internal Medicine Perspectives, 2017 Adrenal collision tumors (ACTs), in which distinct tumors coexist without histological intermingling in the same adrenal gland, are rare and their actual prevalence is unknown. ACTs commonly consist of adrenal cortical adenoma, myelolipoma, or metastatic
Dongyan Liu, Sahayini A. Kumar
doaj +1 more source
Adrenal pheochromocytoma incidentally discovered in a patient with parkinsonism [PDF]
, 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
Embolization in an adrenocortical carcinoma as palliative therapy [PDF]
, 1999 Background: With an annual incidence of 0.2% of new cases per 100,000 inhabitants, adrenocortical carcinoma is rare. In advanced tumor only palliative treatment modalities are practicable. Because of scarcity of the tumor, standard treatment has not been
Braunschweig, R. +5 more
core +1 more source
Эндокринная хирургия, 2012 Contemporary development of two hormonal active tumors in different layers of one adrenal gland is occurring extremely rarely in clinical practice. Authors adduce their own clinical cases of competitive adrenal tumors.
V O Bondarenko +3 more
doaj +1 more source