eISSN: 2084-9869
ISSN: 1233-9687
Polish Journal of Pathology
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1/2009
vol. 60
 
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abstract:

Primary cutaneous CD30+ lymphoproliferative disorder – a 10-year follow-up. A case report and differential diagnosis

Joanna Szpor
,
Grzegorz Dyduch
,
Krystyna Gałązka
,
Jan Bahyrycz
,
Anastazja Stój
,
Romana Tomaszewska

Pol J Pathol 2009; 1: 43-48
Online publish date: 2009/05/05
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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
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