Primary atrophic profound linear scleroderma

Mordechai M. Tarlow, Vlasta Dragoš, Borut Žgavec, Tomaž Lunder, Robert Schwartz

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

We describe an 18-year-old male with primary atrophic profound linear scleroderma. It was not preceded by an inflammatory reaction or sclerosis, but it involved the subcutaneous and deeper tissues of the fingers. It did not involve the dermis, or show either discoloration or changes in texture. Involvement of deeper tissue and the progression of the disease suggest atypical primary atrophic profound linear scleroderma. Our case of primary atrophic profound linear scleroderma appears to be a unique variant of localized scleroderma.

Original languageEnglish (US)
Pages (from-to)25-29
Number of pages5
JournalActa Dermatovenerologica Alpina, Pannonica et Adriatica
Volume13
Issue number1
StatePublished - Mar 1 2004

All Science Journal Classification (ASJC) codes

  • Dermatology
  • Infectious Diseases

Keywords

  • Atrophic
  • Circumscribed
  • Linear
  • Male patient
  • Profound
  • Scleroderma

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  • Cite this

    Tarlow, M. M., Dragoš, V., Žgavec, B., Lunder, T., & Schwartz, R. (2004). Primary atrophic profound linear scleroderma. Acta Dermatovenerologica Alpina, Pannonica et Adriatica, 13(1), 25-29.