Stomach cancer, familial
An inherited form of stomach cancer
Familial Stomach Cancer | |
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[[File:|250px|]] | |
Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Abdominal pain, nausea, vomiting, weight loss |
Complications | Metastasis, malnutrition |
Onset | Typically in adulthood |
Duration | Long-term |
Types | N/A |
Causes | Genetic mutations (e.g., CDH1 gene) |
Risks | Family history, genetic predisposition |
Diagnosis | Genetic testing, endoscopy, biopsy |
Differential diagnosis | N/A |
Prevention | N/A |
Treatment | Surgery, chemotherapy, targeted therapy |
Medication | N/A |
Prognosis | Varies depending on stage and treatment |
Frequency | Rare |
Deaths | N/A |
Familial stomach cancer is a hereditary form of stomach cancer that occurs due to genetic mutations passed down through families. It is a rare condition but has significant implications for affected individuals and their relatives.
Genetics[edit | edit source]
Familial stomach cancer is often associated with mutations in the CDH1 gene, which encodes the protein E-cadherin. This protein is crucial for cell adhesion, and its dysfunction can lead to increased cancer risk. Other genetic mutations may also contribute to familial stomach cancer, but CDH1 is the most well-known.
Symptoms[edit | edit source]
The symptoms of familial stomach cancer are similar to those of sporadic stomach cancer and may include:
- Abdominal pain
- Nausea and vomiting
- Weight loss
- Loss of appetite
- Dysphagia (difficulty swallowing)
Diagnosis[edit | edit source]
Diagnosis of familial stomach cancer involves a combination of genetic testing and clinical evaluation. Individuals with a family history of stomach cancer may undergo genetic testing to identify mutations in the CDH1 gene. Endoscopic examination and biopsy are used to confirm the presence of cancerous cells in the stomach.
Treatment[edit | edit source]
Treatment options for familial stomach cancer depend on the stage of the disease and may include:
- Surgery: Total or partial gastrectomy to remove cancerous tissue.
- Chemotherapy: Use of drugs to kill cancer cells.
- Targeted therapy: Drugs that specifically target cancer cell mechanisms.
Prognosis[edit | edit source]
The prognosis for familial stomach cancer varies. Early detection and treatment can improve outcomes, but the overall prognosis depends on the stage at diagnosis and the effectiveness of the treatment.
Prevention[edit | edit source]
For individuals with a known genetic predisposition, preventive measures may include regular surveillance endoscopies and consideration of prophylactic gastrectomy to reduce cancer risk.
Also see[edit | edit source]
Health science - Medicine - Gastroenterology - edit |
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Diseases of the esophagus - stomach |
Halitosis | Nausea | Vomiting | GERD | Achalasia | Esophageal cancer | Esophageal varices | Peptic ulcer | Abdominal pain | Stomach cancer | Functional dyspepsia | Gastroparesis |
Diseases of the liver - pancreas - gallbladder - biliary tree |
Hepatitis | Cirrhosis | NASH | PBC | PSC | Budd-Chiari | Hepatocellular carcinoma | Acute pancreatitis | Chronic pancreatitis | Pancreatic cancer | Gallstones | Cholecystitis |
Diseases of the small intestine |
Peptic ulcer | Intussusception | Malabsorption (e.g. Coeliac, lactose intolerance, fructose malabsorption, Whipple's) | Lymphoma |
Diseases of the colon |
Diarrhea | Appendicitis | Diverticulitis | Diverticulosis | IBD (Crohn's, Ulcerative colitis) | IBS | Constipation | Colorectal cancer | Hirschsprung's | Pseudomembranous colitis |
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Contributors: Prab R. Tumpati, MD