Endocrine Neoplasm

An endocrine organ’s epithelial cells develo** a benign or malignant tumor are called endocrine neoplasm. Pituitary adenoma, pituitary carcinoma, thyroid carcinoma, carcinoid tumor, and neuroendocrine carcinoma are some cases of endocrine neoplasm. Wermer’s syndrome, also known as multiple endocrine neoplasia type 1 (MEN 1), is an uncommon condition that results in tumors in the small intestine, stomach, and endocrine glands. The parathyroid, pancreas, and pituitary glands typically develop tumors and emit an overabundance of hormones that might cause disease in MEN 1. The tumors are mostly benign and incurable. Excessive hormones might result in a wide range of symptoms and indications. These include fatigue, bone aches, fractures, kidney stones, and stomach or intestine ulcers. The MEN1 gene itself is also known as MEN1. Individuals are more likely to experience endocrine tumors and other MEN1 symptoms if they have a mutation (alteration) in the MEN1 gene.