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Oncocytic adrenal tumour presenting as Cushing syndrome: rare presentation of a rare tumour
The Egyptian Journal of Internal Medicine, 2014 Oncocytic neoplasms are well recognized in organs such as the kidney, thyroid and salivary glands. They are seen rarely in other sites such as the adrenal cortex.
Abhishek Singhai, Subodh Banzal
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Case Reports in Endocrinology, 2017 The adrenal glands produce a variety of hormones that play a key role in the regulation of blood pressure, electrolyte homeostasis, metabolism, immune system suppression, and the body’s physiologic response to stress.
Roberto Ruiz-Cordero +5 more
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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
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Inhibin Alpha Expression in Human Tumors: A Tissue Microarray Study on 12,212 Tumors
Biomedicines, 2022 As a result of its expression in corresponding normal cell types, inhibin alpha (INHA) is used as an immunohistochemical marker for adrenocortical neoplasms and testicular or ovarian sex cord stromal tumors.
Sören Weidemann +24 more
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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
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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
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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
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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
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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
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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
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