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MALT Lymphom

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by

Elke Wolfinger

on 20 April 2010

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Transcript of MALT Lymphom

MALT-Lymphom Mucosa Associated Lymphatic Tissue Extranodales Marginalzonen-B-Zell-Lymphom Entstehung Allgemein primär ausserhalb der Lymphknoten Charakteristikum Primärmanifestation

kein lymphatisches
Parenchym MALT-Lymphom/Magen 7-8% B-Zell Lymphome dritthäufigste Lymphomart in westlicher Welt Erstdiagnose: 60 Jahre Inzidenz: 0,8/100.000 E./J. Ursachen chronische Entzündungen/Infektionen/Autoimmunerkrankungen Helicobacter-Gastritis Magen Speicheldrüse Sjögren-Syndrom Schilddrüse chronische lymphozytäre
Konjunktivitis Hashimoto-Thyreoiditis Symptome uncharakteristisch Appetitlosigkeit Übelkeit diffuses Druckgefühl Schwitzen, Fieber Gewichtsverlust Histopathologische Merkmale zentrozytenartig, monozytoid, lymphozytisch
plasmazellähnlich Therapie frühes Stadium Antibiotika fortgeschrittenes Stadium Operation Strahlen/Chemotherapie Tumorzellen
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