@Article{Szpor2009,
journal="Polish Journal of Pathology",
issn="1233-9687",
volume="60",
number="1",
year="2009",
title="Primary cutaneous CD30+ lymphoproliferative disorder \– a 10-year follow-up.  A case report and differential diagnosis",
abstract="Primary cutaneous CD30+ lymphoproliferative disorders (LPDs) are the second most common group of primary cutaneous T-cell lymphomas (CTCLs). The spectrum of LPDs includes lymphomatoid papulosis (LyP), primary cutaneous anaplastic large cell lymphoma (C-ALCL) and borderline cases. The term \“borderline lesions\” refers to cases where histological features are similar to LyP, but clinically behave as C-ALCL, or to cases where histological features are typical for C-ALCL, but clinically behave as LyP.  We present a clinical and morphological picture of LPD in a 57-year old patient treated in the Department of Oncology and of a relapse after ten years of follow-up and discuss clinical and morphological differential diagnosis and the significance of such diagnosis",
author="Szpor, Joanna
and Dyduch, Grzegorz
and Gałązka, Krystyna
and Bahyrycz, Jan
and Stój, Anastazja
and Tomaszewska, Romana",
pages="43--48",
url="https://www.termedia.pl/Primary-cutaneous-CD30-lymphoproliferative-disorder-8211-a-10-year-follow-up-A-case-report-and-differential-diagnosis,55,12396,1,1.html"
}