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Adrenal cancer is the presence of malignant adrenal tumors, and includes neuroblastoma, adrenocortical carcinoma and some adrenal pheochromocytomas. Most adrenal pheochromocytomas and all adrenocortical adenomas are benign tumors, which do not metastasize or invade nearby tissues, but may cause significant health problems by unbalancing hormones.
Neuroblastoma is one of the peripheral neuroblastic tumors (pNTs) that have similar origins and show a wide pattern of differentiation ranging from benign ganglioneuroma to stroma-rich ganglioneuroblastoma with neuroblastic cells intermixed or in nodules, to highly malignant neuroblastoma.
Other common locations include the adrenal gland, paraspinal retroperitoneum, posterior mediastinum, head, and neck. [1] It is contained within the neuroblastic tumors group, which includes: [3] Ganglioneuroma (benign), Ganglioneuroblastoma (intermediate), Neuroblastoma (aggressive).
Neuroblastic tumors. It is contained within the neuroblastic tumors group, which includes: [3] Ganglioneuroma (benign) Ganglioneuroblastoma (intermediate).
Adrenal cancer most often affects adults in their 40s and 50s and children younger than 5, but it can occur at any time. "When adrenal cancer is found early, there is a chance for cure. But if the ...
Adrenocortical carcinoma (ACC) is an aggressive cancer originating in the cortex (steroid hormone-producing tissue) of the adrenal gland.. Adrenocortical carcinoma is remarkable for the many hormonal syndromes that can occur in patients with steroid hormone-producing ("functional") tumors, including Cushing's syndrome, Conn syndrome, virilization, and feminization.
It was first identified as a "gay cancer" as it mainly affected gay men and was associated with Kaposi's sarcoma, a rare form of cancer linked to weakened immunity. It further spread among other ...
‘It’s produced by our ovaries and adrenal glands, and is important for both reproductive health and general physiology,’ says Dr Ru Ahweyevu, a former NHS GP now working with the Illuminate ...