Evidence map›Paper›PMID 42731003›Full record

ArticleMagyar onkologia2026

[Sentinel lymph node mapping in colorectal and anal tumors from the beginning until now].

Kornél Vajda

Abstract readEnglish Abstract
In one paragraph

Article in Magyar onkologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Kornél VajdaSebészeti Osztály, Bács-Kiskun Megyei Oktató Kórház, Kecskemét, Hungary. drvajdakornel@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSentinel lymph node biopsy in colorectal cancer remains controversial. Lymph node metastasis is the most important prognostic factor, and even in the absence of lymph node metastasis, the risk of local recurrence is 15-20%.

methodsThe sentinel lymph node was identified in vivo by subserosal injection of blue dye or indocyanine green (ICG), and ex vivo by submucosal or subserosal injection. Stained lymph nodes were examined by the pathologist conventionally with hematoxylin-eosin staining, and in cases of negativity, with serial sectioning and immunohistochemistry and/ or RT-PCR.

resultsDespite the high detection rate of 70-99%, sensitivity for macrometastasis is low (33-93.1%), but improves with the detection of micrometastasis. Stage migration based on micrometastasis detection ranged between 5-15%. Aberrant lymphatic drainage occurs in 3.9-7.1% of cases.

conclusionsAt present, the sensitivity of colorectal sentinel lymph node identification is not suitable for guiding treatment, as the false negative rate is high. This is due to the lack of standardization, inadequate patient selection, and the large number of T3-4 stage tumors. Several authors recommend investigating early T1-2 stage tumors, the incidence of which is increasing due to screening.

Indexed as

Anus NeoplasmsColorectal NeoplasmsLymph NodesSentinel Lymph NodeSentinel Lymph Node BiopsyColoring AgentsFemaleHumansImmunohistochemistryIndocyanine GreenLymphatic MetastasisNeoplasm MicrometastasisNeoplasm StagingPredictive Value of TestsPrognosisSensitivity and SpecificityColoring AgentsIndocyanine Green

Identifiers

PMID42731003
PMCPMC13577722

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.