Mixed endothelial tumors of the colon and rectum are rare, poorly understood entities that include a heterogeneous range of tumors with multiple combinations leading to tumors with acute malignant potential. high, medium or low. In the following article, we will learn more about the pathology of these tumors.

Mixed tumors of the colon and rectum, consisting of a combination of epithelial and endocrine factors with both benign and malignant potential, are rare neoplasms. These tumors can occur anywhere in the gastrointestinal tract and are often diagnosed incidentally.

Mixed endothelial tumors of the colon and rectum are a rare entity, noted with unique histology and clinical behavior. The exact pathogenesis of these tumors remains unclear as they are often characterized by histological heterogeneity, making it impossible to make an accurate diagnosis.

The adrenal medulla is the main place to produce catecholamine hormones (adrenaline, noradrenaline,...) which play a role in increasing the activity of the cardiovascular system. Pheochromocytoma with hypercatecholamine secretion is a condition of increased secretion of adrenal medullary hormones, causing consequences affecting the cardiovascular system.

Dermatological neuromas are often painful and affect the patient's quality of life. Dermatological neuroma surgery is the method indicated to effectively treat this disease.

Neuroendocrine tumors can appear in many different locations in the body, so the diagnosis is relatively complicated and can take a certain amount of time. Treatment for neuroendocrine tumors will be selected appropriately after the diagnostic process.

Neuroendocrine tumor is a rather strange name, many people have never heard of it. Neuroendocrine tumors are a relatively complex issue, and the following article will help have the most overview of neuroendocrine tumors.

Neuroendocrine tumors originate in specialized cells of the body's neuroendocrine system. These cells have the characteristics of both hormone-secreting cells and neurons, and are found in all organs of the body, thus neuroendocrine tumors include many different types with different symptoms. symptoms are very different.

These days, more and more people are suffering from neuroendocrine tumors (NETs), especially in the gastrointestinal tract. The disease is very difficult to diagnose, mostly when it is detected at a late stage, the prognosis is severe, and treatment is difficult.

Metformin can directly activate AMPK, leading to inhibition of downstream Akt/mTOR signaling and inhibition of cell proliferation. Among pancreatic cancer patients, being treated with metformin seems to be able to effectively improve symptoms.

The term “mixed endocrine neoplasm” (MANEC) was coined by the World Health Organization in 2010 to refer to a type of cancer with a dual differentiation between adenocarcinoma and neuroendocrine carcinoma, each components represent at least 30% of tumors. In the following article, we will learn about the prognosis of this type of tumor.