Evidence map›Paper›PMID 34143242›Full record

ReviewDer Radiologe2021

[Imaging of renal tumors in children].

J-P Schenk, A Hötker, R Furtwängler, J Fuchs, S W Warmann, N Graf

Abstract readReview
PubMed Publisher
In one paragraph

Review in Der Radiologe, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Surgical Renal Conditions: Role of Imaging Modalities.Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
    Article
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

6 authors at 5 institutions in 2 countries.

J-P SchenkSektion Pädiatrische Radiologie, Klinik für Diagnostische und Interventionelle Radiologie, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Deutschland. Jens-Peter.Schenk@med.uni-heidelberg.de.
A HötkerInstitut für Diagnostische und Interventionelle Radiologie, Universitätsspital Zürich, Zürich, Schweiz.
R FurtwänglerKlinik für Pädiatrische Onkologie und Hämatologie, Universitätskinderklinik, Universitätsklinikum des Saarlandes, Homburg, Deutschland.
J FuchsAbteilung für Kinderchirurgie und Kinderurologie, Universitätsklinikum Tübingen, Tübingen, Deutschland.
S W WarmannAbteilung für Kinderchirurgie und Kinderurologie, Universitätsklinikum Tübingen, Tübingen, Deutschland.
N GrafKlinik für Pädiatrische Onkologie und Hämatologie, Universitätskinderklinik, Universitätsklinikum des Saarlandes, Homburg, Deutschland.
Universitätsklinikum Tübingen · DEUniversitätskinderklinik · DEUniversitätsklinikum des Saarlandes · DEUniversity Hospital Heidelberg · DEUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

clinical/methodological issueRenal tumors in children are treated according to the guidelines of the Renal Tumor Study Group of the International Society of Pediatric Oncology (SIOP-RTSG). Nephroblastoma is the most frequent renal tumor in children. STANDARD RADIOLOGICAL

methodsAfter sonography, magnetic resonance imaging (MRI) is the preferred imaging modality. The task of imaging includes differential diagnosis with the help of morphological and epidemiological criteria. Thorax computed tomography (CT) is introduced for initial staging. METHODOLOGICAL INNOVATIONS: Current studies of diffusion-weighted imaging (DWI)-MRI with analysis of the apparent diffusion coefficient (ADC) histogram indicate the potential to differentiate blastemal or anaplastic high-risk histology nephroblatoma subtypes. Imaging criteria for nephron-sparing surgery are defined and allow an individual therapy option in unilateral and especially in bilateral renal nephroblastoma. PERFORMANCE: In addition to nephroblastoma, the differential diagnosis includes congenital mesoblastic nephroma, malignant rhabdoid tumor of the kidney, clear cell sarcoma and renal cell carcinoma. The diagnosis of nephrogenic rests and nephroblastomatosis is challenging. ACHIEVEMENTS: Diagnostic standardization improves diagnosis and therapy of renal childhood tumors, and new prognostic markers may be introduced in the near future.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsWilms TumorChildHumansKidneyNephrectomyDiffusion-weighted imagingKidney neoplasmsMagnetic resonance imagingNephroblastomaWilms

Identifiers

PMID34143242
OpenAlexW3166231179

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.