Molluscum contagiosum pathophysiology: Difference between revisions

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{{Molluscum contagiosum}}
{{Molluscum contagiosum}}


{{CMG}}
{{CMG}};{{AE}}{{MIR}}
 
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==Overview==
==Overview==
This is a common infection in children and occurs when a child comes into direct contact with a lesion. The virus can spread through contact with contaminated objects, such as towels, clothing, or toys. The virus also spreads by sexual contact. Persons with a weakened immune system (due to conditions such as AIDS) may have a rapidly worse case of molluscum contagiosum.
Molluscum contagiosum is usually transmitted via direct contact with a skin lesion. Following transmission, molluscum contagiosum uses the human cell machinery to replicate. On gross [[pathology]], a central umbilication and punctiform [[vessels]] are characteristic findings of molluscum contagiosum. On [[Electron microscope|electron microscopic]] analysis, typical brick-shaped [[poxvirus]] particles inside the infected tissue are characteristic findings of molluscum contagiosum.
 
==Pathophysiology==
The time from infection to the appearance of lesions ranges from 1 week to 6 months, with an average incubation period of 6 weeks. Diagnosis is made on the clinical appearance.
===Transmission===
In adults, molluscum infections are often [[sexually transmitted]] and usually affect the [[genitals]], lower [[abdomen]], [[buttocks]], and inner thighs.  In rare cases, molluscum infections are also found on the [[lips]], [[mouth]], and eyelids. It is spread through direct contact or shared articles of clothing (including towels).  


===Virology===
MC has no animal reservoir, infecting only [[human]]s, as did [[smallpox]]. However, there are different pox viruses that infect  many other mammals. The infecting human MC virus is a DNA [[Poxviridae|poxvirus]] called the ''[[molluscum contagiosum virus]]'' (MCV).  There are 4 types of MCV, MCV-1 to -4, with MCV-1 being the most prevalent and MCV-2 seen usually in adults and often sexually transmitted. The virus cannot routinely be cultured.
==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 [[Pericarditis pathophysiology#Overview|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==
*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.
*The human molluscum contagiosum virus (MCV) is a DNA [[Poxviridae|poxvirus]]. 
*For an example of a pathogenesis section within a pathophysiology page, click [[Pericarditis pathophysiology#Pathogenesis|here]]
*MCV has no animal reservoir, infecting only [[human]]s.
*MCV replicates in cells [[cytoplasm]]. This may be related to genetic similarity in [[variola]] and [[vaccinia]] viruses more than one-half.
*In adults, molluscum infections are often [[sexually transmitted]] and usually affect the [[genitals]], lower [[abdomen]], [[buttocks]], and inner thighs. In rare cases, molluscum contagiosum infections are also found on the [[lips]], [[mouth]], and eyelids. It spread through direct contact or shared articles of clothing (including towels).
*MCV can commonly cause asymptomatic cutaneous [[Neoplasm|neoplasms]]. Children and sexually active adults as well as persistent opportunistic [[acquired immunodeficiency syndrome]] (AIDS)-associated disease are more sensitive to the virus and more in danger for cutaneous [[neoplasm]]. <ref name="pmid8941326">{{cite journal |vauthors=Fife KH, Whitfeld M, Faust H, Goheen MP, Bryan J, Brown DR |title=Growth of molluscum contagiosum virus in a human foreskin xenograft model |journal=Virology |volume=226 |issue=1 |pages=95–101 |year=1996 |pmid=8941326 |doi=10.1006/viro.1996.0631 |url=}}</ref>
==Genetics==
==Genetics==
*Some diseases are genetic, and have particular inheritance patterns, and express different phenotypes.
*In 1997, Senkevich et al were the first who described [[molluscum contagiosum virus]] (MCV) genome.<ref name="pmid92012142">{{cite journal |vauthors=Senkevich TG, Koonin EV, Bugert JJ, Darai G, Moss B |title=The genome of molluscum contagiosum virus: analysis and comparison with other poxviruses |journal=Virology |volume=233 |issue=1 |pages=19–42 |year=1997 |pmid=9201214 |doi=10.1006/viro.1997.8607 |url=}}</ref>
*The effect that genetics may have on the pathophysiology of a disease can be described in this section.
*MCV possesses 59 genes predicted to code for novel proteins including [[MHC class I|MHC-class I]], [[chemokine]], and [[glutathione peroxidase]] homologs not found in other [[Poxvirus|poxviruses]]. The MCV genomic data is near complete which can allow the investigation of host defense mechanisms. These information also can provide new possibilities for the development of therapeutics for treatment and prevention of the MCV infection.<ref name="pmid9413524">{{cite journal |vauthors=Bugert JJ, Darai G |title=Recent advances in molluscum contagiosum virus research |journal=Arch. Virol. Suppl. |volume=13 |issue= |pages=35–47 |year=1997 |pmid=9413524 |doi= |url=}}</ref><ref name="pmid9201214">{{cite journal |vauthors=Senkevich TG, Koonin EV, Bugert JJ, Darai G, Moss B |title=The genome of molluscum contagiosum virus: analysis and comparison with other poxviruses |journal=Virology |volume=233 |issue=1 |pages=19–42 |year=1997 |pmid=9201214 |doi=10.1006/viro.1997.8607 |url=}}</ref>
==Associated Conditions==
*Molluscum contagiosum inhibits the host [[inflammatory]] response. This unique feature seems to be related to some of the specific genes that are present in its genome.  
*Conditions associated with the disease can be detailed in this section.
*Scientists have sequenced more than 190-kilobase pair genome of MCV. These genome findings have revealed that the virus potentially encodes approximately 182 proteins, 105 of which have direct counterparts in orthopoxviruses (OPV).<ref name="pmid8941326" /> Another study suggests that MCV lacks counterparts to 83 genes of the [[smallpox virus]], including those important in suppression of host responses to [[infection]], [[nucleotide]] [[biosynthesis]], and [[cell proliferation]].<ref name="pmid9413524" />
*For an example of an associated conditions sub-section of pathophysiology, click [[Clubbing pathophysiology#Associated Conditions|here]].
 
==Gross Pathology==
==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.
In a dermoscopic exam of infected tissue the important parts include:
*This section is a good place to include pictures. Search for copyleft images on The Pathology Wiki [http://pathinfo.wikia.coom/wiki/Pathology_Resident_Wiki] and Ask Dr. Wiki [http://askdrwiki.com/mediawiki/index.php?title=Category:Pathology].
*A central umbilication with polylobular, white to yellow amorphous structures
*For an example of this section, click [[Pericarditis pathophysiology#Gross Pathology Images|here]].
*A peripheral crown of radiating or punctiform vessels<ref name="pmid9201214" />
==Microscopic Pathology==
==Microscopic Pathology==
*Microscopic pathology is the disease process as it occurs at the microscopic level.
[[Electron microscope|Electron microscopic]] evaluation of tissue is not a part of routine diagnosis procedure, but if done it may show:<ref name="pmid9201214" />
*This section is a good place to include pictures. Search for copyleft images on The Pathology Wiki [http://pathinfo.wikia.coom/wiki/Pathology_Resident_Wiki] and Ask Dr. Wiki [http://askdrwiki.com/mediawiki/index.php?title=Category:Pathology].
* Typical brick-shaped [[poxvirus]] particles inside the infected tissue which is highly specific for diagnosis
*For an example of this section, click [[Pericarditis pathophysiology#Microscopic Pathology Images|here]].
* [[Electron microscopy]] can also identify infected cells that appear normal on [[light microscopy]]


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
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Latest revision as of 22:45, 29 July 2020

Molluscum contagiosum Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Molluscum contagiosum from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic criteria

History and Symptoms

Physical Examination

Laboratory Findings

X ray

Ultrasound

CT Scan

MRI

Other Imaging Studies

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Mahshid Mir, M.D. [2]

Overview

Molluscum contagiosum is usually transmitted via direct contact with a skin lesion. Following transmission, molluscum contagiosum uses the human cell machinery to replicate. On gross pathology, a central umbilication and punctiform vessels are characteristic findings of molluscum contagiosum. On electron microscopic analysis, typical brick-shaped poxvirus particles inside the infected tissue are characteristic findings of molluscum contagiosum.

Pathogenesis

  • The human molluscum contagiosum virus (MCV) is a DNA poxvirus.
  • MCV has no animal reservoir, infecting only humans.
  • MCV replicates in cells cytoplasm. This may be related to genetic similarity in variola and vaccinia viruses more than one-half.
  • In adults, molluscum infections are often sexually transmitted and usually affect the genitals, lower abdomen, buttocks, and inner thighs. In rare cases, molluscum contagiosum infections are also found on the lips, mouth, and eyelids. It spread through direct contact or shared articles of clothing (including towels).
  • MCV can commonly cause asymptomatic cutaneous neoplasms. Children and sexually active adults as well as persistent opportunistic acquired immunodeficiency syndrome (AIDS)-associated disease are more sensitive to the virus and more in danger for cutaneous neoplasm. [1]

Genetics

  • In 1997, Senkevich et al were the first who described molluscum contagiosum virus (MCV) genome.[2]
  • MCV possesses 59 genes predicted to code for novel proteins including MHC-class I, chemokine, and glutathione peroxidase homologs not found in other poxviruses. The MCV genomic data is near complete which can allow the investigation of host defense mechanisms. These information also can provide new possibilities for the development of therapeutics for treatment and prevention of the MCV infection.[3][4]
  • Molluscum contagiosum inhibits the host inflammatory response. This unique feature seems to be related to some of the specific genes that are present in its genome.
  • Scientists have sequenced more than 190-kilobase pair genome of MCV. These genome findings have revealed that the virus potentially encodes approximately 182 proteins, 105 of which have direct counterparts in orthopoxviruses (OPV).[1] Another study suggests that MCV lacks counterparts to 83 genes of the smallpox virus, including those important in suppression of host responses to infection, nucleotide biosynthesis, and cell proliferation.[3]

Gross Pathology

In a dermoscopic exam of infected tissue the important parts include:

  • A central umbilication with polylobular, white to yellow amorphous structures
  • A peripheral crown of radiating or punctiform vessels[4]

Microscopic Pathology

Electron microscopic evaluation of tissue is not a part of routine diagnosis procedure, but if done it may show:[4]

References

  1. 1.0 1.1 Fife KH, Whitfeld M, Faust H, Goheen MP, Bryan J, Brown DR (1996). "Growth of molluscum contagiosum virus in a human foreskin xenograft model". Virology. 226 (1): 95–101. doi:10.1006/viro.1996.0631. PMID 8941326.
  2. Senkevich TG, Koonin EV, Bugert JJ, Darai G, Moss B (1997). "The genome of molluscum contagiosum virus: analysis and comparison with other poxviruses". Virology. 233 (1): 19–42. doi:10.1006/viro.1997.8607. PMID 9201214.
  3. 3.0 3.1 Bugert JJ, Darai G (1997). "Recent advances in molluscum contagiosum virus research". Arch. Virol. Suppl. 13: 35–47. PMID 9413524.
  4. 4.0 4.1 4.2 Senkevich TG, Koonin EV, Bugert JJ, Darai G, Moss B (1997). "The genome of molluscum contagiosum virus: analysis and comparison with other poxviruses". Virology. 233 (1): 19–42. doi:10.1006/viro.1997.8607. PMID 9201214.

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