Results 11 to 20 of about 1,223,943 (215)

Adrenocortical tumor in a cat secreting more than one type of corticosteroid

open access: yesJournal of Feline Medicine and Surgery Open Reports, 2015
Case summary A 14-year-old, spayed female domestic shorthair cat was evaluated because of a right adrenal mass. The referring veterinarian had started treatment for hypokalemia and systemic arterial hypertension. During the initial evaluation the cat was
Simone Domit Guerios   +2 more
doaj   +2 more sources

Extra-adrenal, non-functional adrenocortical carcinoma presenting with acute abdomen: a case report

open access: yesJournal of Medical Case Reports, 2020
Background Adrenocortical carcinoma is a rare malignancy, with 43% being non-functional. These may arise from adrenal rest anywhere in the embryonic pathway of the adrenal glands.
Alireza Mirsharifi   +4 more
doaj   +1 more source

Advanced adrenocortical carcinoma successfully treated with gemcitabine plus capecitabine as second‐line chemotherapy

open access: yesIJU Case Reports, 2020
Introduction Adrenocortical carcinoma is a rare malignant tumor with an unfavorable prognosis in the advanced stage for which second‐/third‐line chemotherapy is not well established.
Akinaru Yamamoto   +8 more
doaj   +1 more source

Impairment of adrenocortical function associated with increased plasma tumor necrosis factor-alpha and interleukin 6 concentrations in African trypanosomiasis [PDF]

open access: yes, 1994
African sleeping sickness (SS) is a severe, potentially lethal parasitic disease. The treatments of choice are the antiparasitic agents suramin, which is adrenotoxic, and/or melarsoprol. We evaluated the functional integrity of the hypothalamic-pituitary-
Winkelmann, W.   +19 more
core   +2 more sources

Extramitochondrial OPA1 and adrenocortical function [PDF]

open access: yes, 2013
We have previously described that silencing of the mitochondrial protein OPA1 enhances mitochondrial 27 Ca2+ signaling and aldosterone production in H295R adrenocortical cells.
Fülöp, László   +9 more
core   +2 more sources

Adrenocortical cancer: late diagnosis of the disease on the example of a clinical case. Case report

open access: yesТерапевтический архив, 2023
Adrenocortical carcinoma (ACC) is a rare malignant tumor originating in the adrenal cortex and characterized by poor 5-year survival. It occurs with a frequency of 2–4 cases per 2 million in the population. Women are more frequently affected than men and
Evgenia A. Starostina   +9 more
doaj   +1 more source

Dysembryoplastic Neuroepithelial Tumor: A Benign but Complex Tumor of the Cerebral Cortex [PDF]

open access: yes, 2022
Dysembryoplastic neuroepithelial tumor (DNET) is a distinct type of low-grade glioneuronal tumor. Clinically, DNET is highly associated with intractable epilepsy in young children and adolescents.
김세훈
core   +1 more source

A hypoxia risk score for prognosis prediction and tumor microenvironment in adrenocortical carcinoma

open access: yesFrontiers in Genetics, 2022
Background: Adrenocortical carcinoma (ACC) is a rare malignant endocrine tumor derived from the adrenal cortex. Because of its highly aggressive nature, the prognosis of patients with adrenocortical carcinoma is not impressive. Hypoxia exists in the vast
Yuanyuan Deng   +7 more
doaj   +1 more source

A rare presentation of adrenal adenoma in infancy: isolated Cushing`s syndrome

open access: yesThe Turkish Journal of Pediatrics, 2020
Adrenocortical tumors are rare in children. Most of these tumors present with endocrinological manifestations, majority of which with virilizing features alone or in combination with over production of other adrenal hormones.
Oğuzhan Şal   +2 more
doaj   +1 more source

Adrenocortical carcinosarcoma: a case report and review of the literature

open access: yesDiagnostic Pathology, 2010
Adrenocortical carcinosarcoma is an extremely rare and aggressive variant of adrenocortical carcinoma characterized by the presence of both carcinomatous and sarcomatous components, with the latter often showing heterologous differentiation.
Sasaki Kotaro   +4 more
doaj   +1 more source

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