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DOI 10.1016/j.hbpd.2019.04.006

Медицинская библиотека · Hepatobiliary & pancreatic diseases international : HBPD INT · 2019

Chance and challenge of associating liver partition and portal vein ligation for staged hepatectomy.

Xiang Fei, Hu Ze-Min

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Аннотация

BACKGROUND

The associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) was first performed in 2007. The critical patient selection, timing to perform the second stage operation, and minimally invasive technique are three key factors for patient outcomes. The aim of this review is to summarize published data on these three aspects.

DATA SOURCES: Studies were identified by searching PubMed for articles published from January 2007 to October 2018, using the keywords "associating liver partition and portal vein ligation for staged hepatectomy" or "ALPPS" or "in situ split". Studies on colorectal liver metastasis (CRLM), perihilar cholangiocarcinoma (PHC), and hepatocellular carcinoma (HCC) indicated for ALPPS, cutoff values to determine the timing of stage 2, as well as modifications of ALPPS were included.

RESULTS

The mortality of ALPPS for CRLM is declining, for PHC is high. In patients with HCC, essential hypertrophy makes the ALPPS safer. However, the degrees of fibrosis affect the hypertrophy. The future liver remnant volume is still the gold standard to start the second stage. Hepatobiliary scintigraphy plays an important role in quantitatively assessing liver function, whereas cutoff values need to be further calibrated. Less-invasive ALPPS modifications have increased and led to a decreased mortality.

CONCLUSIONS

ALLPS improved the CRLM outcomes; ALPPS is feasible in patients with PHC after failure of portal vein embolization; ALPPS may be an option for HCC patients with major vascular invasion and thrombosis. The simplified and less-invasive ALPPS is the trend.

Для цитирования: Xiang Fei, Hu Ze-Min. Chance and challenge of associating liver partition and portal vein ligation for staged hepatectomy.. Hepatobiliary & pancreatic diseases international : HBPD INT. 2019. DOI: 10.1016/j.hbpd.2019.04.006.

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