Results 51 to 60 of about 114,029 (285)

Uncommon adrenal rest tumors and massive adrenal enlargement in adult with congenital adrenal hyperplasia mimicking metastasis from pleomorphic sarcoma

open access: yesBMC Endocrine Disorders
Background Congenital adrenal hyperplasia (CAH) encompassed a bunch of autosomal recessive disorders characterized by impaired cortisol levels due to an enzymatic deficiency in steroid synthesis.
Pierluigi Mazzeo   +4 more
doaj   +1 more source

Report of two rare cases of adrenal incidentalomas with different origins: revisiting pathological and radiological findings with a short review of the literature

open access: yesJournal of the Egyptian National Cancer Institute, 2020
Background Adrenal tumors can be detected incidentally in 4 to 8% of patients radiologically. Adenomas, pheochromocytomas, and adrenocortical carcinomas represent the most common tumors of the adrenal glands. Rare histopathological findings are uncommon.
M. A. Elbaset   +4 more
doaj   +1 more source

Cortisol Secreting Adrenal Adenoma in a 5 Year Old Child [PDF]

open access: yes, 2011
Adrenal adenoma is a rare endocrinal tumor in children. It can present with features of Cushing's syndrome. We present a case report of five years old female child who came with morbid obesity and hypertension.
Narang, Gursharan Singh   +1 more
core  

Dysfunctional TRIM31 of POMC Neurons Provokes Hypothalamic Injury and Peripheral Metabolic Disorder under Long‐Term Fine Particulate Matter Exposure

open access: yesAdvanced Science, EarlyView.
Particulate matter ≤2.5 µm (PM2.5) elevates risks of neurological and chronic metabolic diseases, but the underlying mechanisms linking PM2.5‐induced central nervous system (CNS) injury to metabolic dysfunction remain unclear. Hypothalamic pro‐opiomelanocortin‐expressing (POMC+) neurons regulate systemic metabolic homeostasis, and tripartite motif ...
Chenxu Ge   +21 more
wiley   +1 more source

Adrenal Collision Tumor: Coexistence of Pigmented Adrenal Cortical Oncocytoma and Ganglioneuroma

open access: yesCase Reports in Surgery, 2016
Background. Adrenal collision tumors (ACTs), in which distinct tumors coexist without intermingling in the same adrenal gland, are rare and their actual prevalence is unknown.
Hye Seung Lee   +3 more
doaj   +1 more source

Difficulties in the radiological diagnosis of mature adrenal teratoma mimicking neuroblastoma in a child [PDF]

open access: yesDigital Diagnostics
The most common adrenal tumor in young children is neuroblastoma, which can be difficult to differentiate from other conditions such as nephroblastoma, adrenal hemorrhage, angiomyolipoma, myelolipoma, and adenoma.
Ekaterina S. Shchelkanova   +2 more
doaj   +1 more source

Bilateral Lipoadenoma of the Adrenal Glands and Humeral Brown Tumor: An Unusual Association

open access: yesCase Reports in Endocrinology, 2021
Adrenal adenolipomas are rare lipomatous adrenal tumors that can be either functional or not. Only 7 cases have been reported in the English literature so far.
N. Messaoudi   +12 more
doaj   +1 more source

Gut Bacteria Improve Depressive Symptoms by Degrading Cortisol into Androgen

open access: yesAdvanced Science, EarlyView.
Chronic stress is an important risk factor for stress‐related disorders such as depression. Stress hormone cortisol is essential for the pathogenesis of stress‐related disorders such as depression. Some gut microbiota degraded cortisol, and improve depressive symptoms.
Xiong Wang   +12 more
wiley   +1 more source

Comparison of adrenal tumor treatment results by different volume of surgical interventions.

open access: yesЭндокринная хирургия, 2016
In recent years detection of various adrenal tumors has increased greatly. Total adrenalectomy remains the standart of surgical managment for adrenal tumors, although, the vast majority of these tumors turn out to be benign on the routine histological ...
Dmitriy J. Semenov   +4 more
doaj   +1 more source

Pheochromocytoma – clinical manifestations, diagnosis and current perioperative management [PDF]

open access: yes, 2019
Pheochromocytoma is a neuroendocrine tumor characterized by the excessive production of catecholamines (epinephrine, norepinephrine, and dopamine). The diagnosis is suspected due to hypertensive paroxysms, associated with vegetative phenomena, due to the
Bratu, Ovidiu G   +6 more
core   +2 more sources

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