4 results match your criteria: "University Hospital Centre Zagreb Department of Dermatology and Venereology[Affiliation]"

Dear Editor, Approximately 25-33% of cutaneous melanomas arise from nevi (1). Shitara et al. suggested that junctional and compound nevi are more likely give rise to melanoma than intradermal nevi, but this has not been definitively confirmed (2).

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Article Synopsis
  • Segmental Darier disease (DD) is a rare skin condition involving mutations in the calcium ATPase pump, with two types: type 1, which follows Blaschko's lines, and type 2, which features increased severity in generalized cases.
  • Type 1 segmental DD is challenging to diagnose due to its late onset, lack of family history, and similar features to other skin conditions like lichen planus and psoriasis.
  • The report documents two cases, highlighting symptoms, dermoscopic findings, histopathological correlations, and effective treatment with tretinoin gel for the first patient.
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Dermoscopic Features of Twin Melanomas of the Lower Leg: A Case Report.

Acta Dermatovenerol Croat

August 2020

Daniela Ledić Drvar, MD, PhD, University Hospital Centre Zagreb Department of Dermatology and Venereology , School of Medicine University of Zagreb, 10000 Zagreb, Šalata 4, Croatia;

Multiple primary malignancies, including melanoma, usually present singly over time rather than simultaneously. Hovewer, approximatelly one third of the patients develop multiple primary melanomas. We present a case of a 57-year-old woman, with two grossly suspicious, unevenly pigmented lesions on her left lower leg measuring up to 8 and 11 mm.

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Dear Editor,We present the case of a 40-year old male patient with lymphomatoid papulosis of a waxing and waning course on whom three biopsies were performed during a 14-year period with no change in histopathological or immunophenotypical characteristics. Lymphomatoid papulosis (LP) is a chronic, recurrent, self-healing papulonodular skin eruption with the histopathologic features of a cutaneous T-cell lymphoma but an often benign and indolent clinical course (1). It is designated as a primary, cutaneous, CD30+ lymphoproliferative disorder.

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