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03.03.2020 | Lymphome | CME-Topic

Kutane Lymphome

Klinik – Diagnostik – Therapie

verfasst von: PD Dr. M. Wobser, Prof. Dr. M. Goebeler

Erschienen in: best practice onkologie | Ausgabe 3/2020

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Zusammenfassung

Kutane Lymphome umfassen prognostisch heterogene Subgruppen. Die Mycosis fungoides ist das häufigste Hautlymphom und weist einen stadienhaften Verlauf (Patches, Plaques, Tumoren, Erythrodermie) auf. Zu den Behandlungsoptionen zählen in frühen Stadien hautgerichtete Therapiemaßnahmen, während in fortgeschrittenen Stadien und beim Sézary-Syndrom Systemtherapien mit z. B. Bexaroten, Interferon oder Brentuximab vedotin indiziert sind. Seltenere T‑Zell-Lymphome wie die CD4-positive Lymphoproliferation oder das akrale CD8-positive Lymphom zeigen im Gegensatz zu den aggressiven peripheren T‑Zell-Lymphomen einen indolenten Verlauf. Auch innerhalb der kutanen B‑Zell-Lymphome finden sich prognostisch differente Entitäten: Während die Lebenserwartung bei kutanem Marginalzonenlymphom und kutanem follikulärem B‑Zell-Lymphom nahezu nicht beeinträchtigt ist, zeigt das kutane großzellige B‑Zell-Lymphom ein hohes Risiko einer systemischen Disseminierung mit vergleichsweise hoher Letalität.

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Titel: Kutane Lymphome
Klinik – Diagnostik – Therapie
verfasst von: PD Dr. M. Wobser
Prof. Dr. M. Goebeler
Publikationsdatum: 03.03.2020
Verlag: Springer Medizin
Schlagwörter: Lymphome
Non-Hodgkin-Lymphome
Zielgerichtete Therapie
Mycosis fungoides
Sezary-Syndrom
Erythrodermien
Lymphomatoide Papulose
Brentuximab vedotin
Erschienen in: best practice onkologie / Ausgabe 3/2020
Print ISSN: 0946-4565
Elektronische ISSN: 1862-8559
DOI: https://doi.org/10.1007/s11654-020-00203-w

Springer Medizin

Zusammenfassung

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