Esophageal cancer

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Esophageal cancer

GI

GI

Anatomy of the pharynx and esophagus
Anatomy of the oral cavity
Anatomy of the salivary glands
Anatomy of the tongue
Anatomy of the anterolateral abdominal wall
Anatomy of the gastrointestinal organs of the pelvis and perineum
Anatomy of the muscles and nerves of the posterior abdominal wall
Anatomy of the peritoneum and peritoneal cavity
Anatomy of the inguinal region
Anatomy clinical correlates: Anterior and posterior abdominal wall
Development of the digestive system and body cavities
Development of the gastrointestinal system
Esophagus histology
Gastrointestinal system anatomy and physiology
Enteric nervous system
Esophageal motility
Gastric motility
Chewing and swallowing
Esophageal web
Achalasia
Zenker diverticulum
Esophageal cancer
Gastroschisis
Esophageal disorders: Pathology review
Esophageal disorders: Clinical
Anatomy of the abdominal viscera: Large intestine
Anatomy of the abdominal viscera: Innervation of the abdominal viscera
Anatomy of the abdominal viscera: Small intestine
Stomach histology
Colon histology
Small intestine histology
Gastrointestinal hormones
Fats and lipids
Pancreatic secretion
Intestinal fluid balance
Proteins
Carbohydrates and sugars
Peritonitis
Pyloric stenosis
Gastritis
Peptic ulcer
Cyclic vomiting syndrome
Gastric cancer
Gastroenteritis
Gastroparesis
Omphalocele
Intestinal atresia
Intestinal malrotation
Hirschsprung disease
Meckel diverticulum
Imperforate anus
Intussusception
Celiac disease
Lactose intolerance
Whipple's disease
Crohn disease
Ulcerative colitis
Microscopic colitis
Bowel obstruction
Volvulus
Abdominal hernias
Inguinal hernia
Femoral hernia
Ischemic colitis
Small bowel ischemia and infarction
Irritable bowel syndrome
Diverticulosis and diverticulitis
Appendicitis
Anal fissure
Hemorrhoid
Anal fistula
Acute pancreatitis
Chronic pancreatitis
Zollinger-Ellison syndrome
Inflammatory bowel disease: Pathology review
Diverticular disease: Pathology review
Gastrointestinal bleeding: Pathology review
Pancreatitis: Pathology review
Congenital gastrointestinal disorders: Pathology review
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Malabsorption syndromes: Pathology review
Appendicitis: Pathology review
Laxatives and cathartics
Acid reducing medications
Antidiarrheals
Clostridium difficile (Pseudomembranous colitis)
Escherichia coli
Vibrio cholerae (Cholera)
Campylobacter jejuni
Helicobacter pylori
Norovirus
Rotavirus
Entamoeba histolytica (Amebiasis)
Giardia lamblia
Cryptosporidium
Ancylostoma duodenale and Necator americanus
Enterobius vermicularis (Pinworm)
Trichinella spiralis
Trichuris trichiura (Whipworm)
Hunger and satiety
Insulin
Somatostatin
Glucagon
Hydration
Essential fructosuria
Galactosemia
Hereditary fructose intolerance
Anatomy of the abdominal viscera: Liver, biliary ducts and gallbladder
Anatomy of the abdominal viscera: Pancreas and spleen
Anatomy of the abdominal viscera: Blood supply of the foregut, midgut and hindgut
Anatomy clinical correlates: Other abdominal organs
Anatomy clinical correlates: Viscera of the gastrointestinal tract
Gallbladder histology
Liver histology
Pancreas histology
Liver anatomy and physiology
Bile secretion and enterohepatic circulation
Familial adenomatous polyposis
Colorectal polyps
Colorectal cancer
Juvenile polyposis syndrome
Peutz-Jeghers syndrome
Carcinoid syndrome
Jaundice
Cirrhosis
Portal hypertension
Wilson disease
Non-alcoholic fatty liver disease
Budd-Chiari syndrome
Cholestatic liver disease
Hepatocellular adenoma
Alcohol-associated liver disease
Autoimmune hepatitis
Primary sclerosing cholangitis
Benign liver tumors
Hepatocellular carcinoma
Reye syndrome
Viral hepatitis
Gallstones
Acute cholecystitis
Chronic cholecystitis
Pancreatic cancer
Pancreatic pseudocyst
Pancreatic neuroendocrine neoplasms
Jaundice: Pathology review
Cirrhosis: Pathology review
Viral hepatitis: Pathology review
Gallbladder disorders: Pathology review
Colorectal polyps and cancer: Pathology review
Hypercholesterolemia: Clinical
Dyslipidemias: Pathology review
Hepatitis C virus
Familial hypercholesterolemia
Hyperlipidemia
Lysosomal storage disorders: Pathology review
Cholesterol metabolism
Gaucher disease (NORD)
Krabbe disease
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Tay-Sachs disease (NORD)
Fabry disease (NORD)
Metachromatic leukodystrophy (NORD)
Leukodystrophy
Abetalipoproteinemia
Hypertriglyceridemia
Disorders of fatty acid metabolism: Pathology review
Crigler-Najjar syndrome
Gilbert's syndrome
Rotor syndrome
Dubin-Johnson syndrome
Biliary atresia
Hepatic encephalopathy
Primary biliary cholangitis
Hemochromatosis
Biliary colic
Ascending cholangitis
Gallstone ileus
Cholangiocarcinoma
Gallbladder carcinoma
Heme synthesis disorders: Pathology review
Cirrhosis: Clinical
Appendicitis: Clinical
Abdominal pain: Clinical
Gastrointestinal bleeding: Clinical
Peptic ulcers and stomach cancer: Clinical
Inflammatory bowel disease: Clinical
Diverticular disease: Clinical
Gallbladder disorders: Clinical
Pancreatitis: Clinical
Hernias: Clinical
Bowel obstruction: Clinical
Abdominal trauma: Clinical
Diarrhea: Clinical
Esophagitis: Clinical
Anal conditions: Clinical
Malabsorption: Clinical
Gastroparesis: Clinical
Gastroesophageal reflux disease (GERD): Clinical
Jaundice: Clinical
Viral hepatitis: Clinical
Transplant rejection
Graft-versus-host disease
Folate (Vitamin B9) deficiency
Vitamin D
Vitamin C deficiency
Vitamin D deficiency
Vitamin B12 deficiency
Niacin (Vitamin B3) deficiency
Vitamin K deficiency
Fat-soluble vitamin deficiency and toxicity: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Vitamins and minerals
Intestinal adhesions

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Esophageal cancer is when malignant or cancerous cells arise in the esophagus. This cancer can appear in any segment of the esophagus and it’s further classified into squamous cell carcinoma and adenocarcinoma - depending on the type of cells it originates from. Squamous cell carcinoma, as you can tell by its name, arises from squamous epithelium. On the other hand, adeno- means gland. So, adenocarcinoma arises from columnar glandular epithelium. Esophageal cancer is generally considered a poor prognosis cancer, because it doesn't cause symptoms until later stages.

The esophagus is a long tube going from the pharynx to the stomach, and it’s connected to the pharynx through the upper esophageal sphincter, and to the stomach through the lower esophageal sphincter. Both relax during swallowing to allow the passage of food or liquids. Additionally, the lower esophageal sphincter is tightly closed between meals to prevent acid reflux. Now, the esophageal wall has four layers - from the outside in, these are the adventitia ; the muscular layer; the submucosa and the mucosa. The mucosa comes into direct contact with food, and it protects the esophageal wall from friction. The mucosa also has three layers of its own: a layer made of stratified squamous epithelium; a layer of connective tissue, called the lamina propria; and a layer of muscle cells, called the muscularis mucosae. Finally, at the lower esophageal sphincter, the squamous epithelium joins the columnar gastric epithelium to form the gastroesophageal junction.

Now, squamous cell carcinoma is the most common type of esophageal cancer worldwide, and it originates in the squamous epithelium of the esophagus, most often in the upper two thirds. When this epithelium is repeatedly exposed to risk factors like alcohol, cigarette smoke, or hot fluids, it gets damaged, so the squamous cells divide to replace the old damaged cells. With each division, there is a risk that a mutation can occur in the genes that are in charge of the cell cycle and cell division. Mutations can occur in tumor suppressor genes, which normally code for proteins that stop the cell cycle or promote apoptosis - so they’re the cell cycle’s very own brake pedal. Or they can occur in proto-oncogenes, which normally code for proteins that promote the cell cycle - so they’re the cell cycle’s accelerator pedal. When this happens, squamous cells start dividing uncontrollably, and more mutations accumulate with each division. So eventually, these mutations might make the cells malignant - meaning they gain the ability to invade neighboring tissues and spread to distant sites.

On the other hand, adenocarcinoma is the most common type of esophageal cancer in the United States of America, and it originates in the columnar glandular epithelium, most often in the lower third of the esophagus. Most frequently, adenocarcinoma develops as a consequence of gastroesophageal reflux disease, or GERD for short. With GERD, the lower esophageal sphincter is weaker than normal, and it allows acid from the stomach to go back up into the esophagus after meals. The presence of acid in the esophagus can lead to Barrett’s esophagus, which is when the squamous epithelium lining the esophagus is replaced by a columnar epithelium, similar to that of the intestines, that’s better adapted to withstand the acidity. This process is called intestinal metaplasia. Over time, just like with squamous cell carcinoma, mutations might accumulate in either tumor suppressor genes or proto-oncogenes that control the division of these metaplastic cells, ultimately resulting in a malignant tumor.

Risk factors for both squamous cell carcinoma and adenocarcinoma include smoking, age over 60 years, and achalasia - which is when the smooth muscle of the lower portion of the esophagus doesn’t work well, making it difficult for food to pass towards the stomach. Specific risk factors for squamous cell carcinoma include alcohol consumption, hot fluids and caustic strictures, which is the narrowing of the esophagus following ingestion of a caustic substance, like household bleach. Other predisposing conditions include Plummer-Vinson syndrome and palmoplantar keratoderma. Plummer-Vinson syndrome associates iron deficiency anemia; glossitis, or tongue inflammation; cheilosis, or inflammation and cracking of the corners of the mouth; and esophageal webs or rings, which are concentric extensions of normal esophageal wall into the esophageal lumen that can cause difficulty swallowing. Palmoplantar keratoderma is a rare disease in which thick patches of skin develop on the hands and feet. The strongest risk factor for adenocarcinoma, on the other hand, is chronic GERD and Barrett's esophagus. Obesity and being a genetically male individual also increase the risk of adenocarcinoma.

Initially, esophageal cancer is asymptomatic. But once it progresses, the most common symptom is progressive dysphagia, which means difficulty swallowing. At first, dysphagia is specific to solid foods, but as the disease progresses, liquids are also hard to swallow. Unfortunately, this is a late symptom. Other symptoms include odynophagia, or pain when swallowing, pyrosis, which is the fancy word for heartburn, pain in the chest or back, vomiting, and weight loss. When the cancer invades and perforates the entire esophageal wall, it can invade the trachea in front of it, forming a fistula. This can cause pulmonary aspiration of esophageal contents, which may cause symptoms like coughing and dyspnea. If the cancer spreads to the diaphragm, it can cause hiccups.

Sources

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  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "Multimodality Assessment of Esophageal Cancer: Preoperative Staging and Monitoring of Response to Therapy" RadioGraphics (2009)
  6. "Imaging the small bowel" Current Opinion in Gastroenterology (2014)
  7. "Oesophageal carcinoma" The Lancet (2013)