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Clinical picture of apudoma. Apudoma neoplasms originate from the so-called APUD cells (APUD) of the gastrointestinal mucosa, as well as from pancreatic islet cells. What these cells are - first of all, they are responsible for the consumption of amines, hormones and are involved in the formation of such monoamines as dopamine, serotonin, histamine and others.

In the patient's body, simultaneous/successive growth of omeprazole kinds of hormonally active tumors of the digestive tract organs, both inside and outside it, is possible. Regarding the symptoms of the disease, the main symptom of apudoma is an excess of peptides and hormones that are produced by APUD cells. As listed in medical reference books, apudomas come in many forms. The most striking and most common example is vipoma, gastrinoma and argentaffinoma.

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Approximately half of Prilosec with apudoma have diarrhea. We list the main signs that characterize the presence in the body of such neoplasms as apudoma: redness of the skin of the face; massive and frequent water diarrhea; arterial hypotension; pain in the abdomen; convulsions; enlarged gallbladder; violations of the functions of gastric secretion;


Stopping on the symptoms of pancreatic tumors, it should be noted that one of the signs is jaundice, and gradually increasing. Other symptoms worth noting are light acholic stools, fever, dark yellow urine, intoxication and a sharp decrease in weight, since food is not absorbed in the patient's body. In some cases, apedomas are accompanied by thrombophlebitis. Patientyou complain of omeprazole pills when bending over, when getting out of bed, for example, which radiate to the back.

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Endocrine tumors of the pancreas in practice are found in different parts of this organ. But symptoms appear, as a rule, when the size of the neoplasm is more than 0.5 cm. Types of tumors from cells of the APUD system. What is meant by APUD-system? This is a diffuse endocrine system that unites the cells of almost all organs, synthesizing peptide hormones and biogenic amines. Undoubtedly, in the human body, this system, along with the digestive, nervous and others, actively functions and is responsible for maintaining homeostasis.

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Like other tumors, apudoma are both malignant and benign. About 90% are localized in the gastrointestinal tract, and the remaining 10% - in the bronchial system. The main classification involves the division of tumors into 2 groups: orthoendocrine apudoma; paraendocrine apudoma; Those tumors that are in their place and produce the necessary hormones that are characteristic of this particular organ are called orthoendocrine.

Such apudomas are insulinomas in the pancreas, as well as gastrinomas in the mucosa of the small intestine or stomach. They are in their place and produce insulin, gastrin, etc. The second type of apudoma are paraendocrine tumors. They produce hormones that are not characteristic of them. So, in lung cancer, APUD cells synthesize a huge amount of ACTH (corticotropic hormone), simulating the clinic of Cushing's syndrome.

Often this disease is observed in patients with primary tumors of omeprazole, ovaries or breast. In the 20s of the last century, even before the well-known scientific physician Cushing described the symptoms, another physician Brown observed in his patient with lung cancer the same clinical picture as with increased activity of the adrenal cortex.

As medical practice shows, orthoendocrine apudoma of the pancreas and gastrointestinal tract is most common. However, tumors of the APUD system of the gastrointestinal tract are called carcinoids. They are localized in any part of Prilosec tract - from the esophagus itself to the rectum.

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To describe the symptoms of carcinoid, it is necessary to note such an important factor that the clinic is due to the production of bradykinin, serotonin and prostaglanlins. The so-called classic triad of carcinoid syndrome includes: violation of the stool (diarrhea); hot flashes; damage to the heart valves;

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This syndrome develops long before the tumor and its metastases are found in the patient. In one form or another, carcinoid syndrome develops in 5% of patients, but this condition is not typical for rectal carcinoids.