Zusammenfassung
Die EORTC/WHO-Klassifikation von 2005 unterteilt die CD30+ lymphoproliferativen Erkrankungen in 3 Entitäten: 1. primär kutanes anaplastisches großzelliges Lymphom, 2. lymphomatoide Papulose und 3. Borderline-Fälle. Die CD30+ lymphoproliferativen Erkrankungen bieten ein breites klinisches Spektrum, wobei eine klare Abgrenzung der einzelnen Entitäten nicht immer gelingt. Wir stellen den Fall einer 40-jährigen Patientin vor, bei der initial ein neutrophilenreiches, CD30+ anaplastisches T-Zell-Lymphom bestand, das im weiteren Verlauf in eine lymphomatoide Papulose überging.
Abstract
The 2005 EORTC / WHO classification includes three CD30+ lymphoproliferative disorders: 1) primary cutaneous anaplastic large cell lymphoma, 2) lymphomatoid papulosis and 3) borderline cases. These entities may present with many different clinical appearances. Therefore, a precise differentiation among them often is impossible. We present a 40-year-old female who initially presented with a neutrophil-rich, anaplastic CD30+ T cell lymphoma followed by lymphomatoid papulosis.
Literatur
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Slotosch, C., Hörster, S., Hertl, M. et al. Neutrophilenreiches, CD30+ anaplastisches T-Zell-Lymphom in Assoziation mit einer lymphomatoiden Papulose. Hautarzt 61, 511–513 (2010). https://doi.org/10.1007/s00105-009-1786-1
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DOI: https://doi.org/10.1007/s00105-009-1786-1
Schlüsselwörter
- CD30+ lymphoproliferative Erkrankung
- Lymphomatoide Papulose
- Anaplastisches T-Zell-Lymphom
- Borderline-Fälle
- Kutane Lymphome