[Type I and II collagens and mast cells expression in the skin lesions from the patients with localized scleroderma]

Dorota Wielowieyska-Szybińska1, Anna Wojas-Pelc, Grzegorz Dyduch

  • 1Katedra i Klinika Dermatologii, Collegium Medicum, Uniwersytet Jagielloński, Kraków.

Przeglad Lekarski
|August 30, 2008
PubMed

Insights

Localized scleroderma subtypes, morphea en plaques (MP) and atrophoderma Pasini-Pierini (APP), show distinct collagen and mast cell differences. MP exhibits higher collagen expression, while APP has more mast cells, indicating varied fibrotic processes.

Area of Science:

  • Dermatology
  • Pathology
  • Immunohistochemistry

Background:

  • Morphea en plaques (MP) and atrophoderma Pasini-Pierini (APP) are classified as localized scleroderma (LS) types.
  • Despite classification, MP and APP present distinct clinical manifestations.
  • Both conditions involve complex fibrotic processes in the dermis, including collagen and extracellular matrix deposition, with potential mast cell involvement.

Purpose of the Study:

  • To quantitatively assess the expression of type I and III collagens.
  • To determine the number of mast cells within skin lesions of patients diagnosed with APP and MP.
  • To investigate the relationship between collagen expression, mast cell counts, and disease characteristics in APP and MP.

Main Methods:

  • Immunohistochemical analysis was employed to detect and quantify type I and III collagens.
  • Mast cell populations were identified and counted in dermal biopsies.
  • 36 patients with either APP or MP were included in the study.

Main Results:

  • Patients with APP demonstrated significantly lower expression of type I and III collagens compared to those with MP.
  • Type I collagen expression decreased over time exclusively in MP patients; no similar trend was observed for type III collagen.
  • High collagen expression (types I and III) was more prevalent in the active disease phase of MP.
  • Mast cell counts were elevated in APP patients relative to MP patients.
  • In MP, mast cell numbers increased with disease duration, correlating with lower collagen expression.

Conclusions:

  • Distinct differences in collagen deposition and mast cell infiltration exist between APP and MP.
  • The findings suggest divergent pathomechanisms underlying the fibrotic processes in these localized scleroderma subtypes.
  • Further research into the roles of collagen and mast cells could inform targeted therapeutic strategies for MP and APP.

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