Zusammenfassung
Das Rektumkarzinom verhält sich aufgrund seiner lymphatischen Ausbreitungswege anders als das Kolonkarzinom und hat insbesondere ein höheres lokoregionäres Rezidivrisiko. Trotz vieler technischer Variationen ist die En-bloc-Resektion des Tumors einschließlich der regionalen Gefäßversorgung unverändert der zentrale Eckpfeiler der chirurgischen Therapie. Systematische pathoanatomische Erkenntnisse zur perirektalen Tumorausbreitung, ein besseres Verständnis der Kontinenzmechanismen und ein optimiertes Instrumentarium führten dazu, dass ca. 85% der Rektumkarzinome kontinenzerhaltend operiert werden können. Bei Tumoren des oberen Rektumdrittels stellt das kein Problem dar, die Rekonstruktion erfolgt durch eine End-zu-End-Deszendorektostomie. Bei Tumoren des mittleren und distalen Rektumdrittels ist die totale mesorektale Exzision obligat. Hier stellt die Kolonpouch-anale Anastomose mit vorgeschaltetem Kolon-J-Reservoir die derzeitige Standardrekonstruktion dar. Die lokale Exzision (endoskopisch oder chirurgisch transanal) beschränkt sich auf uT1-Low-risk-Tumoren. Neoadjuvante Therapieansätze haben einen festen Stellenwert bei extraperitoneal gelegenen wandüberschreitenden oder nodalpositiven Tumoren.
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Willis, S., Schumpelick, V. (2010). Rektumkarzinom. In: Siewert, J.R., Rothmund, M., Schumpelick, V. (eds) Praxis der Viszeralchirurgie Onkologische Chirurgie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-03808-2_48
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