Evidence map›Paper›PMID 32246350›Full record

ReviewJapanese journal of radiology2020

FDG-PET/CT imaging findings of hepatic tumors and tumor-like lesions based on molecular background.

Kumi Ozaki, Kenichi Harada, Noboru Terayama, Nobuyuki Kosaka, Hirohiko Kimura, Toshifumi Gabata

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Japanese journal of radiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Hepatic Vascular Shunts Mimicking Malignant Lesions onMolecular imaging and radionuclide therapy · 2026
    Article
  2. Tumor Characterization Using [Pharmaceuticals (Basel, Switzerland) · 2026
    Article
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  11. A prospective study ofAnnals of nuclear medicine · 2024
    Article
  12. Article
  13. Is Prone Position [Diagnostics (Basel, Switzerland) · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Review
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  19. Review
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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 3 institutions in 1 country.

Kumi OzakiDepartment of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan. ozakik-rad@umin.org.
Kenichi HaradaDepartment of Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
Noboru TerayamaDepartment of Radiology, Takaoka City Hospital, Takaoka, Japan.
Nobuyuki KosakaDepartment of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.
Hirohiko KimuraDepartment of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.
Toshifumi GabataDepartment of Radiology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
University of Fukui · JPKanazawa University · JPKouseiren Takaoka Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The usefulness of whole-body 18-fluoro-2-deoxyglucose (FDG)-fluorodeoxyglucose positron emission (PET)/computed tomography (CT) is established for assessment of disease staging, detection of early disease recurrence, therapeutic evaluation, and predicting prognosis in various malignancies; and for evaluating the spread of inflammation. However, the role of FDG-PET/CT for the liver is limited because CT and magnetic resonance imaging (MRI) can provide an accurate diagnosis of most tumors. In addition, in other potentially useful roles there are several pitfalls in the interpretation of FDG uptake in PET/CT imaging. Accurate evaluation demands knowledge of the FDG uptake of each lesion, including potential negative and positive uptakes, and requires an understanding of the underlying background of the molecular mechanisms. The degree of FDG uptake is dependent on cellular metabolic rate and the expression of glucose transporter, hexokinase, and glucose-6-phosphatase, which in turn are closely affected by biological characteristics such as pathological category (e.g., adenocarcinoma, squamous cell carcinoma, small cell cancer, transitional cell cancer, neuroendocrine tumor, sarcoma, lymphoma), tumor differentiation, histological behavior (e.g., solid, cystic, mucinous), and intratumoral alterations (e.g., necrosis, degeneration, hemorrhage). Correlation with the CT and MRI findings, which also precisely depict the pathological findings, is important to avoid misdiagnosis.

Indexed as

Fluorodeoxyglucose F18RadiopharmaceuticalsAdultAgedAged, 80 and overDiagnosis, DifferentialFemaleHumansLiverLiver NeoplasmsMaleMiddle AgedPositron Emission Tomography Computed TomographyFluorodeoxyglucose F18RadiopharmaceuticalsFluorodeoxyglucoseGlucose-6-phosphatase complexGlucose transporterHepatic tumorsPositron emission/computed tomography

Identifiers

PMID32246350
OpenAlexW3014168226

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.