Pemphigoid

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1. resembling pemphigus.
2. a group of skin disorders similar to but clearly distinguishable from pemphigus.

  • bullous p. — an autoimmune disease of skin and oral mucosa with vesicles, bullae and ulcerations; occurs rarely in dogs and humans.
  • cicatricial p. — a form that involves the oral and ocular mucosa.
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Pemphigoid
Classification and external resources
ICD-10 L12
ICD-9 694.5
DiseasesDB 9760
MeSH D010391

Pemphigoid is a group of uncommon and rare autoimmune blistering skin diseases. As its name indicates, pemphigoid is similar to pemphigus,[1] but, unlike pemphigus, pemphigoid does not feature acantholysis.[2]

Pemphigoid is more common than pemphigus, and is slightly more common in women than in men. It is also more common in people over 60 years of age than it is in younger people.

Contents

Classificiation

IgG

The forms of pemphigoid are considered to be connective tissue autoimmune skin diseases. There are several types:

Bullous and Cicatricial pemphigoids usually affect persons who are over age 60.[3][4] Gestational pemphigoid occurs during pregnancy,[5] typically in the second or third trimester, and/or immediately following pregnancy.

IgA

Pemphigoid is usually considered to be mediated by IgG, but IgA-mediated forms have also been described.[6]

IgA Pemphigoid rarely affect the mouth.

See also

References


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