Results 21 to 30 of about 48,160 (221)
Virilizing adrenocortical oncocytoma in a toddler
Journal of Pediatric Surgery Case Reports, 2017 Functioning adrenocortical oncocytomas are extremely rare and most reported patients are 40–60 yr of age. To our knowledge, only 6 cases of functioning adrenocortical oncocytomas have been reported in childhood.
Merna El Khansa +3 more
doaj +1 more source
Endokrynologia Polska, 2017 INTRODUCTION Adrenal neoplasms comprise about 10% of all tumours affecting this organ and constitute a significant, at first diagnostic and subsequently therapeutic, problem, especially since a relatively high proportion of neoplastic lesions are ...
R. Pogorzelski +11 more
semanticscholar +1 more source
Are physiological oscillations physiological?
The Journal of Physiology, EarlyView., 2023 Abstract figure legend Mechanisms and functions of physiological oscillations. Abstract Despite widespread and striking examples of physiological oscillations, their functional role is often unclear. Even glycolysis, the paradigm example of oscillatory biochemistry, has seen questions about its oscillatory function.
Lingyun (Ivy) Xiong, Alan Garfinkel
wiley +1 more source
KIAA0101 is overexpressed, and promotes growth and invasion in adrenal cancer. [PDF]
PLoS ONE, 2011 BACKGROUND:KIAA0101 is a proliferating cell nuclear antigen-associated factor that is overexpressed in some human malignancies. Adrenocortical neoplasm is one of the most common human neoplasms for which the molecular causes are poorly understood ...
Meenu Jain +3 more
doaj +1 more source
Feminizing Adrenocortical Carcinoma Without Gynecomastia
Oman Medical Journal, 2017 Malignant feminizing adrenocortical tumors are exceedingly rare. Their main presentation is gynecomastia. In these estrogen secreting tumors (with or without other adrenocortical hormones) lack of gynecomastia is exceptional as in our case. A 44-year-old
Farida Chentli1*, +3 more
doaj +1 more source
Myxoid adrenal cortical adenoma and isolated adrenal myelolipoma
Наука и инновации в медицине, 2020 Objectives– to reveal the clinical, morphological and hormonal characteristics of patients operated on for isolated adrenal myelolipoma and myxoid adenomas with adrenal myelolipoma.
A. A. Lisitsyn +4 more
doaj +1 more source
Frontiers in Endocrinology, 2015 Adrenocortical tumors (ACT) in children are very rare and are most frequently diagnosed in the context of the Li-Fraumeni syndrome, a multiple cancer syndrome linked to germline mutations of the tumor suppressor gene TP53 with loss of heterozygosity in ...
Enzo eLalli, Bonald C. Figueiredo
doaj +1 more source
Acquisition order of Ras and p53 gene alterations defines distinct adrenocortical tumor phenotypes. [PDF]
PLoS Genetics, 2012 Sporadic adrenocortical carcinomas (ACC) are rare endocrine neoplasms with a dismal prognosis. By contrast, benign tumors of the adrenal cortex are common in the general population. Whether benign tumors represent a separate entity or are in fact part of
Maryline Herbet +3 more
doaj +1 more source
Intestinal obstruction caused by neoplasms in two cows
Ciência Rural, 2016 : In cattle, abdominal tumors leading to partial or total intestinal obstruction are rare. Here, it is described the clinico-pathological findings of two cows with intestinal obstruction by neoplasms.
Antônio Carlos Lopes Câmara +3 more
doaj +1 more source
Rare Tumors, 2016 Adenomatoid tumors are neoplasms of mesothelial origin, usually occurring in the male and female genital tracts. Extragenital localization sites such as adrenal glands are rare but have been reported.
Brankica Krstevska +2 more
doaj +1 more source