Category
page 1Gastrointestinal cancer
pancreatic cancer
endocrine gland cancer located in the pancreas
esophageal cancer
gastrointestinal system cancer that is located in the esophagus
anal cancer
Is a rare disease which it is caused in most of the cases by the infection of the Human Papilloma Virus (HPV).

carcinoid tumor
A carcinoid (also carcinoid tumor) is a slow-growing type of neuroendocrine tumor originating in the cells of the neuroendocrine system. In some cases, metastasis may occur. Carcinoid tumors of the midgut (jejunum, ileum, appendix, and cecum) are associated with carcinoid syndrome.
familial adenomatous polyposis
autosomal dominant disease that is has material basis in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer
small intestine cancer
intestinal cancer that is located in the small intestine
cutaneous squamous-cell carcinoma
skin carcinoma that has material basis in squamous cells
gastrointestinal stromal tumor
human disease

hepatoblastoma
Hepatoblastoma is a malignant liver cancer occurring in infants and children and composed of tissue resembling fetal liver cells, mature liver cells, or bile duct cells. They usually present with an abdominal mass. The disease is most commonly diagnosed during a child's first three years of life. Alpha-fetoprotein (AFP) levels are commonly elevated, but when AFP is not elevated at diagnosis the prognosis is poor.
pseudomyxoma peritonei
appendix cancer that is characterized by progressive accumulation of mucus-secreting tumor cells within the abdomen and pelvis
appendix cancer
cancer that is located in the appendix
Gardner's syndrome
congenital disorder of digestive system
Krukenberg tumor
Human disease
MALT lymphoma
non-Hodgkin lymphoma that has material basis in mucosal tissue involved in antibody production
duodenum cancer
small intestine cancer that is located in the beginning section of the small intestine
juvenile polyposis syndrome
autosomal dominant disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum

gastrointestinal system cancer
organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system
Intraductal papillary mucinous neoplasm
medical condition
linitis plastica
Human disease
Stauffer syndrome
medical condition
digestive system cancer
type of cancer that afflicts the digestive system
gastric lymphoma
Human disease