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Gastric ulcer pathophysiology

Overview

  • The overview section should include the disease name in the first sentence.
  • The goal is to summarize the pathophysiology page in several sentences. This section can be the same as the pathophysiology segment on the overview page.
  • To see an example of an overview section on a symptoms page, click here.

Template

  • The overview is highly dependent on the individual disease pathophysiology. There is no specific template preference for the first sentence.

Template Sentences:

Template Sentence 1: [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
Template Sentence 2: Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
Template Sentence 3: On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Template Sentence 4: On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Template Sentence 5: [Disease name] is transmitted in [mode of genetic transmission] pattern.
Template Sentence 6: [Disease/malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
Template Sentence 7: Development of [disease name] is the result from multiple genetic mutations.
Template Sentence 8: Genes involved in the pathogenesis of [disease name] include [gene1], [gene2], and [gene3].
Template Sentence 9: The progression to [disease name] usually involves the [molecular pathway].
Template Sentence 10: The pathophysiology of [disease name] depends on the histological subtype.

Examples:

Example 1: Spores of C. difficile are transmitted via the fecal-oral route to the human host.
Example 2: Following ingestion, the acid-resistant spores of C. difficile are able to survive the human gastric acidity.
Example 3: Following ingestion, Shigella spp. uses the M cells of the GI tract to invade the epithelial cells of the large intestine.
Example 4: Following transcytosis and macrophage apoptosis, Shigella avoids extracellular exposure and spreads intercellularly using actin polymerization processes (rocket propulsion).
Example 5: On gross pathology, hyperemia with development of ulcers and edema are characteristic findings of shigellosis.
Example 6: On microscopic histopathological analysis, infiltration of PMN and inflammatory pseudomembrane formation are characteristic findings of shigellosis.
Example 7: Duchenne muscular dystrophy is transmitted in an X-linked recessive pattern.
Example 8: Malignant melanoma arises from the epidermal melanocytes, which are neural crest cells normally involved in the synthesis of melanin (a brown pigment with photoprotective properties).
Example 9: Development of melanoma is the result of multiple genetic mutations.
Example 10: Genes involved in the pathogenesis of melanoma include p53, RB, ARF, and BRAF.
Example 11: The progression to melanoma usually involves the serine-threonine kinases of the MAPK/ERK pathway (mitogen-activated protein kinase) following mutation of either the N-RAS or BRAF oncogene.
Example 12: The pathophysiology of gallbladder cancer depends on the histological subtype.

Pathogenesis

Pathogenesis is the mechanism by which a certain factor causes disease (pathos = disease, genesis = development). The term can also be used to describe the development of the disease, whether it is acute, chronic, or recurrent. It can also be used to describe whether the disease causes inflammation, malignancy, necrosis etc.

Template Sentences

IF the pathogenesis of the disease is unclear:

  • The exact pathogenesis of [disease name] is not fully understood.
  • It is thought that Gastric ulcer disease is the result of self-digestion which occurs due to an excess of autopeptic power in gastric juice over the defensive power of gastric mucosa and is mediated by two major factors which disrupt mucosal resistance to injury: Helicobacter pylori (formerly Campylobacter pylori) infection in 75% cases[1] and nonsteroidal anti-inflammatory drugs (NSAIDs) |[2]
  • Helicobacter pylori-gram negative bacteria,spiral-shaped, urease positive.
    • It secrete cytotoxins and produce virulence factors like Cag A, VacA, and OipA.Cytotoxin-associated gene pathogenicity encodes protein CagA and vacuolating cytotoxin VacA aids in the colonization of gastric mucosa and it modulates host's immune system.Cag A and Vac A leads to activation of IL-8 which leads to inflammation of gastric mucosa.[3]
    • It secretes various enzyme :Urease,Phospholipases,Alcohol dehydrogenase and Catalases- causes damage the host gastric muscosa by generating toxic metabolities[4][5][6]


IF the disease has a known genetic component:

  • [Disease name] is transmitted in [mode of genetic transmission] pattern.
  • Genes involved in the pathogenesis of [disease name] include [gene1], [gene2], and [gene3].

IF certain pathology findings are characteristic of the disease:

  • On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
  • On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].

Other relevant information may include the action of the pathogen on a molecular level, the body’s response, whether or not mutations play a role in the disease development, whether the pathophysiology of the disease is different among subgroups of the disease, etc. Additional template sentences are listed below. Due to the highly variable nature of pathophysiology among various diseases, this list is not comprehensive.

  • [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
  • The development of [disease name] is the result of multiple genetic mutations.
  • The progression to [disease name] usually involves the [molecular pathway].
  • The pathophysiology of [disease/malignancy] depends on the histological subtype.
  • For an example of a pathogenesis section within a pathophysiology page, click here

Genetics

  • Some diseases are genetic, and have particular inheritance patterns, and express different phenotypes.
  • The effect that genetics may have on the pathophysiology of a disease can be described in this section.

Template sentences

  • [Disease name] is transmitted in [mode of genetic transmission] pattern.
  • Genes involved in the pathogenesis of [disease name] include [gene1], [gene2], and [gene3].

Associated Conditions

  • Conditions associated with the disease can be detailed in this section.

Template sentences

  • The most important conditions/diseases associated with [disease name] include:
    • Condition 1: A brief explanation of the condition and its association with the disease
    • Condition 2: A brief explanation of the condition and its association with the disease

For an example of an associated conditions sub-section of pathophysiology, click here.

Gross Pathology

  • Gross pathology refers to macroscopic or larger scale manifestations of disease in organs, tissues and body cavities. The term is commonly used by pathologist to refer to diagnostically useful findings made during the gross examination portion of surgical specimen processing or an autopsy.
Template Sentences
  • Template Sentences 1: On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
  • Template Sentence 2: The most important characteristics of [disease name] on gross pathology are:
    • Organ 1: List of characteristics + image
    • Organ 2: List of characteristics + image
    • Organ 3: List of characteristics + image
  • This section is a good place to include pictures. Search for copyleft images on The Pathology Wiki [1] and Ask Dr. Wiki [2].
  • For an example of this section, click here.

Microscopic Pathology

  • Microscopic pathology is the disease process as it occurs at the microscopic level.
  • Template Sentence 1: On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
  • Template Sentence 2: The most important histopathological characteristics of [disease name] are summarized in the table below:
Organs Light microscope Electron microscope Images
Organ 1 Characteristic 1a Characterstic 1b Image 1
Organ 2 Characteristic 2a Characterstic 2b Image 2
Organ 3 Characterstic 3a Characterstic 3b Image 3
  • This section is a good place to include pictures. Search for copyleft images on The Pathology Wiki [3] and Ask Dr. Wiki [4].
  • For an example of this section, click here.

References

  • References should be cited for the material that you have put on your page. Type in {{reflist|2}}.This will generate your references in small font, in two columns, with links to the original article and abstract.
  • For information on how to add references into your page, click here.


Template:WikiDoc Sources

  1. ↑ "Pathogenesis of Peptic Ulcer and Implications for Therapy — NEJM".
  2. ↑ url=http://www.nejm.org/doi/full/10.1056/NEJM199003293221307 |title=Pathogenesis of Peptic Ulcer and Implications for Therapy — NEJM |format= |work= |accessdate=}}
  3. ↑ Logan RP (1996). "Adherence of Helicobacter pylori". Aliment. Pharmacol. Ther. 10 Suppl 1: 3–15. PMID 8730255.
  4. ↑ Mobley HL (1996). "The role of Helicobacter pylori urease in the pathogenesis of gastritis and peptic ulceration". Aliment. Pharmacol. Ther. 10 Suppl 1: 57–64. PMID 8730260.
  5. ↑ Nilius M, Malfertheiner P (1996). "Helicobacter pylori enzymes". Aliment. Pharmacol. Ther. 10 Suppl 1: 65–71. PMID 8730261.
  6. ↑ Slomiany BL, Kasinathan C, Slomiany A (1989). "Lipolytic activity of Campylobacter pylori: effect of colloidal bismuth subcitrate (De-Nol)". Am. J. Gastroenterol. 84 (10): 1273–7. PMID 2801678.
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