Zusammenfassung
Unter dem Begriff der hormonell induzierten Diarrhö werden eine Reihe sehr heterogener Krankheitsbilder zusammengefaßt. Die gemeinsamen Leitsymptome dieser Erkrankungen sind 1. wäßrige Durchfälle, die bei Nahrungskarenz persistieren, also sekretorischer Natur sind, und 2. autonome Produktion eines oder mehrerer Hormone in Pankreas oder Gastrointestinaltrakt oder gelegentlich auch anderen Organen.1 Zollinger U. Ellison (1955) erkannten als erste den Zusammenhang zwischen Inselzelltumoren des Pankreas und therapieresistenten peptischulzerösen Läsionen des oberen Gastrointestinaltrakts. Das pathogenetische Bindeglied Gastrin, welches über die gastrale Hypersekretion von Säure und Pepsin zur Ulkusbildung führt, wurde von Gregory et al. (1960) aus einem Zollinger-Ellison-Tumor extrahiert. Die nicht selten zu beobachtenden Durchfälle führte man zunächst auf die begleitende Steatorrhö als Folge der Inaktivie- rung pankreatischer Enzyme durch die Ubersäuerung des Intestinaltrakts zurück (Maynard U. Point 1958); in rascher Folge erschienen jedoch Fallberichte, in denen wäßrige Durchfälle und Hypokaliämie im Vordergrund standen (Priest u. Alexander 1957), peptische Ulzera hingegen fehlen konnten (Ellison U. Wilson 1964). Verner U. Morrison (1958) beschrieben 2 Fälle von Inselzellade-nom mit letaler Diarrhö und Hypokaliämie; peptische Läsionen waren nicht vorhanden, jedoch wurde die Magensäureproduktion nicht gemessen. Die Abgrenzung dieses Syndroms vom Zollinger-Ellison-Syndrom geschah durch Knappe et al. (1966) und Marks et al.
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Ruppin, H., Soergel, K.H. (1983). Hormonell induzierte Diarrhöen. In: Bommer, W., et al. Dünndarm B. Handbuch der inneren Medizin, vol 3 / 3 / B. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68897-3_11
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