Tytuł pozycji:
Primary cutaneous CD30+ lymphoproliferative disorder : a 10-year follow-up : a case report and differential diagnosis
- Tytuł:
-
Primary cutaneous CD30+ lymphoproliferative disorder : a 10-year follow-up : a case report and differential diagnosis
- Autorzy:
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Bahyrycz, Jan
Gałązka, Krystyna
Szpor, Joanna
Tomaszewska, Romana
Dyduch, Grzegorz
Stój, Anastazja
- Data publikacji:
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2009
- Język:
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angielski
- Prawa:
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Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Na tych samych warunkach 4.0 Międzynarodowa
http://creativecommons.org/licenses/by-nc-sa/4.0/pl/legalcode
- Linki:
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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 Link otwiera się w nowym oknie
- Dostawca treści:
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Repozytorium Uniwersytetu Jagiellońskiego
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Przejdź do źródła Link otwiera się w nowym oknie
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.
