Esophageal disorders: Pathology review

Last updated: November 01, 2022

Esophageal disorders: Pathology review

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Acyanotic congenital heart defects: Pathology review
Cyanotic congenital heart defects: Pathology review
Atherosclerosis and arteriosclerosis: Pathology review
Coronary artery disease: Pathology review
Peripheral artery disease: Pathology review
Valvular heart disease: Pathology review
Cardiomyopathies: Pathology review
Heart failure: Pathology review
Supraventricular arrhythmias: Pathology review
Ventricular arrhythmias: Pathology review
Heart blocks: Pathology review
Aortic dissections and aneurysms: Pathology review
Pericardial disease: Pathology review
Endocarditis: Pathology review
Hypertension: Pathology review
Shock: Pathology review
Vasculitis: Pathology review
Cardiac and vascular tumors: Pathology review
Dyslipidemias: Pathology review
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Diabetes mellitus: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Pituitary tumors: Pathology review
Hypopituitarism: Pathology review
Diabetes insipidus and SIADH: Pathology review
Multiple endocrine neoplasia: Pathology review
Congenital gastrointestinal disorders: Pathology review
Esophageal disorders: Pathology review
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Inflammatory bowel disease: Pathology review
Malabsorption syndromes: Pathology review
Diverticular disease: Pathology review
Appendicitis: Pathology review
Gastrointestinal bleeding: Pathology review
Colorectal polyps and cancer: Pathology review
Pancreatitis: Pathology review
Gallbladder disorders: Pathology review
Jaundice: Pathology review
Viral hepatitis: Pathology review
Cirrhosis: Pathology review
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Immunodeficiencies: T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Combined T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Phagocyte and complement dysfunction: Pathology review
Pigmentation skin disorders: Pathology review
Acneiform skin disorders: Pathology review
Papulosquamous and inflammatory skin disorders: Pathology review
Vesiculobullous and desquamating skin disorders: Pathology review
Skin cancer: Pathology review
Back pain: Pathology review
Rheumatoid arthritis and osteoarthritis: Pathology review
Seronegative and septic arthritis: Pathology review
Gout and pseudogout: Pathology review
Systemic lupus erythematosus (SLE): Pathology review
Scleroderma: Pathology review
Sjogren syndrome: Pathology review
Bone disorders: Pathology review
Bone tumors: Pathology review
Myalgias and myositis: Pathology review
Neuromuscular junction disorders: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Congenital neurological disorders: Pathology review
Headaches: Pathology review
Seizures: Pathology review
Cerebral vascular disease: Pathology review
Traumatic brain injury: Pathology review
Spinal cord disorders: Pathology review
Dementia: Pathology review
Central nervous system infections: Pathology review
Movement disorders: Pathology review
Demyelinating disorders: Pathology review
Adult brain tumors: Pathology review
Pediatric brain tumors: Pathology review
Neurocutaneous disorders: Pathology review
Congenital renal disorders: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Acid-base disturbances: Pathology review
Electrolyte disturbances: Pathology review
Renal failure: Pathology review
Nephrotic syndromes: Pathology review
Nephritic syndromes: Pathology review
Urinary incontinence: Pathology review
Urinary tract infections: Pathology review
Kidney stones: Pathology review
Renal and urinary tract masses: Pathology review
Disorders of sex chromosomes: Pathology review
Prostate disorders and cancer: Pathology review
Testicular tumors: Pathology review
Uterine disorders: Pathology review
Ovarian cysts and tumors: Pathology review
Cervical cancer: Pathology review
Vaginal and vulvar disorders: Pathology review
Benign breast conditions: Pathology review
Breast cancer: Pathology review
Complications during pregnancy: Pathology review
Congenital TORCH infections: Pathology review
Choanal atresia
Laryngomalacia
Allergic rhinitis
Nasal polyps
Upper respiratory tract infection
Sinusitis
Laryngitis
Retropharyngeal and peritonsillar abscesses
Bacterial epiglottitis
Nasopharyngeal carcinoma
Respiratory distress syndrome: Pathology review
Cystic fibrosis: Pathology review
Pneumonia: Pathology review
Tuberculosis: Pathology review
Deep vein thrombosis and pulmonary embolism: Pathology review
Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Obstructive lung diseases: Pathology review
Restrictive lung diseases: Pathology review
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Lung cancer and mesothelioma: Pathology review
Coronary artery disease: Clinical
Heart failure: Clinical
Syncope: Clinical
Pericardial disease: Clinical
Valvular heart disease: Clinical
Infective endocarditis: Clinical
Cardiomyopathies: Clinical
Hypertension: Clinical
Hypercholesterolemia: Clinical
Diabetes mellitus: Clinical
Hyperthyroidism: Clinical
Parathyroid conditions and calcium imbalance: Clinical
Hypothyroidism and thyroiditis: Clinical
Thyroid nodules and thyroid cancer: Clinical
Pituitary adenomas and pituitary hyperfunction: Clinical
Hypopituitarism: Clinical
Cushing syndrome: Clinical
Adrenal insufficiency: Clinical
Adrenal masses and tumors: Clinical
MEN syndromes: Clinical
Esophageal disorders: Clinical
Esophagitis: Clinical
Gastroesophageal reflux disease (GERD): Clinical
Peptic ulcers and stomach cancer: Clinical
Gastroparesis: Clinical
Diarrhea: Clinical
Malabsorption: Clinical
Inflammatory bowel disease: Clinical
Colorectal cancer: Clinical
Diverticular disease: Clinical
Anal conditions: Clinical
Gastrointestinal bleeding: Clinical
Gallbladder disorders: Clinical
Pancreatitis: Clinical
Jaundice: Clinical
Viral hepatitis: Clinical
Cirrhosis: Clinical
Immunodeficiencies: Clinical
Fever of unknown origin: Clinical
Fat-soluble vitamin deficiency and toxicity: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Zinc deficiency and protein-energy malnutrition: Pathology review
Anemia: Clinical
Leukemia: Clinical
Thrombocytopenia: Clinical
Lymphoma: Clinical
Bleeding disorders: Clinical
Myeloproliferative neoplasms: Clinical
Thrombophilia: Clinical
Plasma cell disorders: Clinical
Blood products and transfusion: Clinical
Pneumonia: Clinical
Urinary tract infections: Clinical
Meningitis, encephalitis and brain abscesses: Clinical
Bites and stings: Clinical
Hypernatremia: Clinical
Hyponatremia: Clinical
Hyperkalemia: Clinical
Hypokalemia: Clinical
Metabolic and respiratory acidosis: Clinical
Metabolic and respiratory alkalosis: Clinical
Toxidromes: Clinical
Medication overdoses and toxicities: Pathology review
Environmental and chemical toxicities: Pathology review
Acute kidney injury: Clinical
Chronic kidney disease: Clinical
Nephritic and nephrotic syndromes: Clinical
Asthma: Clinical
Chronic obstructive pulmonary disease (COPD): Clinical
Cystic fibrosis: Clinical
Diffuse parenchymal lung disease: Clinical
Venous thromboembolism: Clinical
Acute respiratory distress syndrome: Clinical
Pleural effusion: Clinical
Pneumothorax: Clinical
Lung cancer: Clinical
Joint pain: Clinical
Rheumatoid arthritis: Clinical
Seronegative arthritis: Clinical
Systemic lupus erythematosus (SLE): Clinical
Sjogren syndrome: Clinical
Inflammatory myopathies: Clinical
Vasculitis: Clinical
Antihistamines for allergies
Glucocorticoids
Sympatholytics: Alpha-2 agonists
Adrenergic antagonists: Presynaptic
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
ACE inhibitors, ARBs and direct renin inhibitors
Thiazide and thiazide-like diuretics
Calcium channel blockers
cGMP mediated smooth muscle vasodilators
Class I antiarrhythmics: Sodium channel blockers
Class II antiarrhythmics: Beta blockers
Class III antiarrhythmics: Potassium channel blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Lipid-lowering medications: Statins
Lipid-lowering medications: Fibrates
Miscellaneous lipid-lowering medications
Positive inotropic medications
Loop diuretics
Antiplatelet medications
Hyperthyroidism medications
Hypothyroidism medications
Insulins
Hypoglycemics: Insulin secretagogues
Miscellaneous hypoglycemics
Adrenal hormone synthesis inhibitors
Mineralocorticoids and mineralocorticoid antagonists
Laxatives and cathartics
Antidiarrheals
Acid reducing medications
Anticoagulants: Heparin
Anticoagulants: Warfarin
Anticoagulants: Direct factor inhibitors
Thrombolytics
Hematopoietic medications
Ribonucleotide reductase inhibitors
Topoisomerase inhibitors
Platinum containing medications
Anti-tumor antibiotics
Microtubule inhibitors
DNA alkylating medications
Monoclonal antibodies
Antimetabolites for cancer treatment
Protein synthesis inhibitors: Aminoglycosides
Antimetabolites: Sulfonamides and trimethoprim
Antituberculosis medications
Miscellaneous cell wall synthesis inhibitors
Protein synthesis inhibitors: Tetracyclines
Cell wall synthesis inhibitors: Penicillins
Miscellaneous protein synthesis inhibitors
Cell wall synthesis inhibitors: Cephalosporins
DNA synthesis inhibitors: Metronidazole
DNA synthesis inhibitors: Fluoroquinolones
Integrase and entry inhibitors
Nucleoside reverse transcriptase inhibitors (NRTIs)
Protease inhibitors
Hepatitis medications
Non-nucleoside reverse transcriptase inhibitors (NNRTIs)
Neuraminidase inhibitors
Herpesvirus medications
Azoles
Echinocandins
Miscellaneous antifungal medications
Anthelmintic medications
Antimalarials
Anti-mite and louse medications
Osmotic diuretics
Carbonic anhydrase inhibitors
Potassium sparing diuretics
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Acetaminophen (Paracetamol)
Non-steroidal anti-inflammatory drugs
Opioid agonists, mixed agonist-antagonists and partial agonists
Antigout medications
Osteoporosis medications

Transcript

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A 33-year-old named Ravi came to the clinic because he has difficulty swallowing food and water over the last 3 months. Physical examination shows significant weight loss, of 7-kg or 15-lb, since his last visit 4 months ago. Esophageal manometry shows incomplete lower esophageal sphincter relaxation in response to swallowing, while barium swallow reveals a dilated esophagus with an area of distal stenosis. At the same time, a 62-year-old man named Frank comes to the clinic because of bad breath, regurgitation of food overnight, and trouble swallowing food. He has had these symptoms for several months. He denies fever, chills, nausea, vomiting, or weight loss. Physical examination shows a mass on the side of the neck. v

Now, both Ravi and Frank have some form of the esophageal disorder. Esophageal disorders can be subdivided into: inflammatory esophageal disorders, or esophagitis, which are characterized by an inflammation of the esophageal lining along with dysphagia, and odynophagia; functional esophageal disorders, which affect the muscles and nerves that control the motility of the esophagus and cause intermittent dysphagia for solids and liquids; and mechanical esophageal disorders, which are characterized by the blockage of the passageway and they typically cause progressive dysphagia for solids.

Inflammatory esophageal disorders, also known as esophagitis, are characterized by an inflammation of the esophageal lining and based on the cause, they are also subdivided into several types.

First, there’s reflux esophagitis, which is associated with the reflux of gastric acid from the stomach back into the esophagus. Alternatively, pill-induced esophagitis, where a medication injures the esophagus thereby causing inflammation and possible upper GI bleeding. It is associated with medications such as nonsteroidal anti-inflammatory drugs or NSAIDs, bisphosphonates, tetracyclines, iron, and potassium chloride. In caustic esophagitis, caustic agents, such as strong acids like vinegar or strong bases like detergents, cause esophageal lesions.

The next one is infectious esophagitis, which is most commonly seen in immunocompromised individuals, such as HIV-positive individuals. The most common causes of HIV associated esophagitis include candida albicans, herpes simplex virus 1, and cytomegalovirus. A high yield fact to remember is that with candida esophagitis, the upper endoscopy will show patches of adherent, white or grey pseudomembranes on the underlying mucosa. The histopathology reveals yeast cells and pseudohyphae that invade mucosal cells of the esophagus. Any attempt to remove the pseudomembrane can cause bleeding in the underlying mucosa. With HSV esophagitis, a high yield fact to remember is that an upper endoscopy will show small vesicles and lesions that look like small punched-out ulcers; while the histopathology reveals eosinophilic intranuclear inclusions in multinuclear squamous cells at the margin of the ulcer. For your exam, you have to know that these inclusions are called Cowdry type A inclusions. CMV esophagitis features linear ulcers on the upper endoscopy, while histopathology reveals both intranuclear and cytoplasmic inclusions.

Finally, we have eosinophilic esophagitis, also called allergic esophagitis, which is characterized by eosinophils that infiltrated into the lining of the esophagus. This occurs as a reaction to food allergens and it can lead to dysphagia and food impaction. Eosinophilic esophagitis is most commonly seen in individuals who have other allergies and a high yield fact that’s often used as a clue is that their esophagitis will be unresponsive to GERD therapy. During an upper endoscopy, eosinophilic esophagitis is characterized by linear furrows and esophageal rings, which are thin mucosal bands that surround the esophagus.

Moving on to functional esophageal conditions, which include achalasia, diffuse esophageal spasm, and sclerodermal esophageal dysmotility.

Achalasia is when there’s impaired esophageal motility and the inability to relax the lower esophageal sphincter. The most common cause of primary achalasia is idiopathic degeneration or damage of postganglionic inhibitory neurons in the myenteric, or Auerbach, plexus of the esophagus. There’s also secondary achalasia which is caused by Trypanosoma Cruzi infection that cause Chagas disease, or extraesophageal malignancies. So normally, the neuron in the myenteric plexus release inhibitory neurotransmitters, such as nitric oxide and vasoactive intestinal peptide, which relax the lower esophageal sphincter. Eventually, the lack of inhibitory neurotransmitters leads to an increased resting lower esophageal sphincter tone, and this obstruction leads to dilatation of the esophagus. These individuals present with progressive dysphagia for both solids and liquids, regurgitation of undigested food, aspiration, chest pain, heartburn, and weight loss. In addition, they have an increased risk for esophageal squamous cell and adenocarcinoma.

For diagnosis, remember for your exam that barium swallow in achalasia reveals dilatation of the esophagus above the obstruction and tapering of the lower part of the esophagus near the lower esophageal sphincter. This is also known as the bird’s beak sign. The gold standard for diagnosis is esophageal manometry, which measures the strength and coordination of the esophageal contractions when a person swallows. This measurement is done at multiple levels, including the upper, middle, and lower esophagus, as well as the lower esophageal sphincter.

Now, you might be asked to analyze manometry findings on your exam so let’s go over this. Normally when a person swallows, involuntary contractions of the pharyngeal muscles propel the food into the esophagus. Propulsion of the food bolus is followed by the contraction of the cricopharyngeal muscle which initiates the peristaltic wave of the esophagus. This contraction is shown as an upward deflection on the upper esophageal manometry. Next, the middle esophageal manometry reflects normal peristalsis of the middle part of the esophagus. Finally, the lower esophageal manometry suggests the decrease in the lower esophageal sphincter that corresponds to its relaxation and the passing of the bolus into the stomach.

Now for your exam, you have to know that individuals with achalasia have normal findings in the upper part of the esophagus, decrease or absence of peristalsis in the middle part of the esophagus, and high pressure in the lower esophageal sphincter. For treatment, the obstruction can be corrected with balloon dilation or increased tone can managed with local injection of botulinum toxin.

In diffuse esophageal spasm, there’s periodic, non-peristaltic contractions that occur simultaneously with each other. In contrast to achalasia, diffuse esophageal spasm is associated with a normal lower esophageal sphincter tone since the spasms occur in the walls of the esophagus. For your exam, you have to know that these disorganized involuntary esophageal contractions can cause intermittent dysphagia for both solids and liquids, and occasional retrosternal chest pain. It’s important to note that the pain can mimic angina but it’s not associated with physical activity and is not relieved by rest; however this can still resemble unstable angina. Therefore, every person that is suspected of having diffuse esophageal spasm should undergo a complete cardiac work-up to rule out any cardiac pathology.

Sources

  1. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  2. "Robbins Basic Pathology" Elsevier (2017)
  3. "Rosen's Emergency Medicine - Concepts and Clinical Practice E-Book" Elsevier Health Sciences (2013)
  4. "Endoscopic assessment of oesophagitis: clinical and functional correlates and further validation of the Los Angeles classification" Gut (1999)
  5. "How I Approach Dysphagia" Current Gastroenterology Reports (2019)
  6. "Iron deficiency anemia and Plummer–Vinson syndrome: current insights" Journal of Blood Medicine (2017)
  7. "Morphometric and anthropometric analysis of Killian's triangle" The Laryngoscope (2010)