Peutz-Jeghers-Syndrom (mit Laugier Hunziker syndrom)
Zuletzt aktualisiert: 2022-11-16
Autor(en): Navarini A.
ICD11: LD2D.0
Zuletzt aktualisiert: 2022-11-16
Autor(en): Navarini A.
ICD11: LD2D.0
Peutz 1921, Jeghers 1949.
Peutz-Touraine-Jeghers Syndrom, Hutchinson-Weber-Peutz Syndrom, Polyposis intestinalis et ephelides inversae, Lentigopolypose, Periorifiziale Lentiginose, Melanoplakie mit Darmpolypen.
Genodermatosen, familiäres Lentiginose-Syndrom.
Hohes Lebenszeitrisiko für Malignome: Pankreas, Bronchial, endokrine Tumoren, neuroendokrine Karzinome, Schilddrüsenkarzinom, Kolon, Cervix, Ovar, Hoden.
Neoplasie-Vorsorge.
Beggs et al. Gut 2010.
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