Results 31 to 40 of about 4,267,390 (291)

Current Approaches in the Minimally Invasive Surgical Treatment of Adrenal Tumors [PDF]

open access: yes, 2017
The use of imaging modalities and minimally invasive surgery plays an important role in the current management of adrenal tumors. Ultrasonography frequently allows for the incidental diagnosis of adrenal masses.
Tartaglia Nicola   +13 more
core   +1 more source

Unilateral orchiectomy of a testicular adrenal rest tumor: Case report and review of management options

open access: yesUrology 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

Single-nuclei transcriptomes from human adrenal gland reveal distinct cellular identities of low and high-risk neuroblastoma tumors

open access: yesNature Communications, 2021
Childhood neuroblastoma has a remarkable variability in outcome. Age at diagnosis is one of the most important prognostic factors, with children less than 1 year old having favorable outcomes. Here we study single-cell and single-nuclei transcriptomes of
O. Bedoya-Reina   +15 more
semanticscholar   +1 more source

Modulation of Autophagy in Adrenal Tumors. [PDF]

open access: yesFront Endocrinol (Lausanne), 2022
Adrenal masses are one of the most common tumors in humans. The majority are benign and non-functioning and therefore do not require immediate treatment.
Sousa D, Pereira SS, Pignatelli D.
europepmc   +2 more sources

An exceedingly rare adrenal collision tumor: adrenal adenoma–metastatic breast cancer–myelolipoma

open access: yesJournal 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

European Society of Endocrinology Clinical Practice Guidelines on the Management of Adrenocortical Carcinoma in Adults, in collaboration with the European Network for the Study of Adrenal Tumors.

open access: yesEuropean Journal of Endocrinology, 2018
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone producing tumor with variable prognosis. The purpose of these guidelines is to provide clinicians with best possible evidence-based recommendations for clinical management of ...
M. Fassnacht   +9 more
semanticscholar   +1 more source

Preclinical Cushing's syndrome in adrenal incidentalomas [PDF]

open access: yes, 1992
Adrenal tumors are usually diagnosed by clinical symptoms of hormone excess. The increasing use of ultrasound and computed tomography results in the detection of a substantial number of incidentally discovered adrenal tumors.
Winkelmann, W.   +5 more
core   +1 more source

Investigation of biochemical composition of adrenal gland tumors by means of FTIR [PDF]

open access: yes, 2016
The application of Fourier transform infrared (FTIR) microspectroscopy for the analysis of biomolecular composition of adrenal gland tumors is described.
Maciej Kolodziej   +17 more
core   +1 more source

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz   +3 more
wiley   +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.
Travis, W.   +7 more
core   +1 more source

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