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Erschienen in: Die Gynäkologie 1/2019

05.10.2018 | Präeklampsie | Gynäkologie aktuell

Was Morbus Osler und Präeklampsie (nicht) gemeinsam haben

verfasst von: PD Dr. med. Angela Köninger, Buu-Phuc Nguyen, Alexandra Gellhaus, Freya Dröge, Rainer Kimmig, Urban Geisthoff

Erschienen in: Die Gynäkologie | Ausgabe 1/2019

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Zusammenfassung

Das Rendu-Osler-Weber-Syndrom Typ 1 (hereditäre hämorrhagische Teleangiektasie 1, HHT1) und die Präeklampsie basieren beide auf einer pathologischen Funktion des Endoglins. Patienten mit HHT1 haben einen heterozygoten Endoglingendefekt, der zu einer systemischen vaskulären Dysplasie führt. Bei der Präeklampsie produziert der Trophoblast lösliches Endoglin (sEng). sEng wirkt wie ein „Antikörper“, der das mütterliche Endoglinrezeptorsubstrat hemmt und antagonisiert. Dies führt zu einer endothelialen Dysfunktion. Im Beitrag werden 2 verschiedene endoglinbedingte Erkrankungen miteinander verglichen, um eine fundiertere Einsicht in die spezifischen klinischen Merkmale zu gewinnen. Diskutiert werden ferner Managementoptionen für schwangere Patientinnen mit HHT.
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Metadaten
Titel
Was Morbus Osler und Präeklampsie (nicht) gemeinsam haben
verfasst von
PD Dr. med. Angela Köninger
Buu-Phuc Nguyen
Alexandra Gellhaus
Freya Dröge
Rainer Kimmig
Urban Geisthoff
Publikationsdatum
05.10.2018
Verlag
Springer Medizin
Erschienen in
Die Gynäkologie / Ausgabe 1/2019
Print ISSN: 2731-7102
Elektronische ISSN: 2731-7110
DOI
https://doi.org/10.1007/s00129-018-4336-z

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