Acantholysis: Difference between revisions

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[[File:Diseases_of_Swine_25-5.png|thumb|right]] '''Acantholysis''' is a [[pathological]] condition characterized by the loss of [[cohesion]] between [[keratinocytes]], the predominant cell type in the [[epidermis]]. This process leads to the breakdown of the [[epidermal]] structure, resulting in the formation of [[blisters]] and [[erosions]] on the [[skin]] and [[mucous membranes]].
{{Infobox medical condition
| name            = Acantholysis
| image          = [[File:Diseases_of_Swine_25-5.png|250px]]
| caption        = Histological image showing acantholysis
| field          = [[Dermatology]]
| synonyms        =
| symptoms        = [[Blistering]], [[erosion (dermatology)|erosions]], [[ulcer (dermatology)|ulcers]]
| complications  = [[Infection]], [[scarring]]
| onset          = Varies depending on underlying cause
| duration        = Chronic or acute
| causes          = [[Autoimmune disease]], [[genetic disorder]], [[infection]]
| risks          =
| diagnosis      = [[Skin biopsy]], [[immunofluorescence]]
| differential    = [[Pemphigus]], [[bullous pemphigoid]], [[dermatitis herpetiformis]]
| prevention      = Depends on underlying cause
| treatment      = [[Corticosteroids]], [[immunosuppressants]], [[antibiotics]]
| medication      =
| prognosis      = Varies; can be managed with treatment
| frequency      = Rare
}}
'''Acantholysis''' is a [[pathological]] condition characterized by the loss of [[cohesion]] between [[keratinocytes]], the predominant cell type in the [[epidermis]]. This process leads to the breakdown of the [[epidermal]] structure, resulting in the formation of [[blisters]] and [[erosions]] on the [[skin]] and [[mucous membranes]].


==Pathophysiology==
==Pathophysiology==
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==References==
==References==
{{Reflist}}
{{Reflist}}
[[Category:Dermatology]]
[[Category:Dermatology]]
[[Category:Autoimmune diseases]]
[[Category:Autoimmune diseases]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Skin conditions resulting from errors in metabolism]]
[[Category:Skin conditions resulting from errors in metabolism]]
{{medicine-stub}}
{{medicine-stub}}

Latest revision as of 23:00, 3 April 2025

Acantholysis
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Blistering, erosions, ulcers
Complications Infection, scarring
Onset Varies depending on underlying cause
Duration Chronic or acute
Types N/A
Causes Autoimmune disease, genetic disorder, infection
Risks
Diagnosis Skin biopsy, immunofluorescence
Differential diagnosis Pemphigus, bullous pemphigoid, dermatitis herpetiformis
Prevention Depends on underlying cause
Treatment Corticosteroids, immunosuppressants, antibiotics
Medication
Prognosis Varies; can be managed with treatment
Frequency Rare
Deaths N/A


Acantholysis is a pathological condition characterized by the loss of cohesion between keratinocytes, the predominant cell type in the epidermis. This process leads to the breakdown of the epidermal structure, resulting in the formation of blisters and erosions on the skin and mucous membranes.

Pathophysiology[edit]

Acantholysis occurs due to the disruption of desmosomes, which are specialized structures that facilitate cell-to-cell adhesion in the epidermis. The loss of desmosomal function can be caused by various factors, including autoimmune diseases, genetic mutations, and infections. The detachment of keratinocytes leads to the formation of intraepidermal clefts and vesicles.

Causes[edit]

Acantholysis can be seen in several dermatological conditions, including:

  • Pemphigus vulgaris: An autoimmune disease where autoantibodies target desmogleins, components of desmosomes.
  • Pemphigus foliaceus: Another autoimmune condition affecting desmogleins, but typically less severe than pemphigus vulgaris.
  • Hailey-Hailey disease: A genetic disorder caused by mutations in the ATP2C1 gene, leading to defective calcium transport and impaired desmosomal function.
  • Darier's disease: A genetic condition resulting from mutations in the ATP2A2 gene, affecting calcium homeostasis and desmosomal integrity.
  • Herpes simplex virus infection: The virus can cause acantholysis by directly infecting keratinocytes and disrupting their adhesion.

Clinical Presentation[edit]

Patients with acantholysis may present with:

  • Blisters: Fluid-filled lesions that can rupture, leading to erosions.
  • Erosions: Areas where the epidermis has been lost, exposing the underlying dermis.
  • Crusting: Formation of dried exudate on the skin surface.
  • Pruritus: Itching, which may accompany the lesions.

Diagnosis[edit]

The diagnosis of acantholysis is typically made through:

  • Clinical examination: Observation of characteristic skin lesions.
  • Skin biopsy: Histopathological examination revealing loss of keratinocyte cohesion and intraepidermal clefting.
  • Direct immunofluorescence: Detection of autoantibodies in autoimmune conditions like pemphigus vulgaris.

Treatment[edit]

The treatment of acantholysis depends on the underlying cause:

Prognosis[edit]

The prognosis of acantholysis varies depending on the underlying condition and the effectiveness of treatment. Autoimmune conditions like pemphigus vulgaris can be chronic and require long-term management, while infections may resolve with appropriate antiviral therapy.

See Also[edit]

References[edit]

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