Evidence map›Paper›PMID 20299300›Full record

ReviewCancer imaging : the official publication of the International Cancer Imaging Society2010

The indeterminate adrenal lesion.

Anju Sahdev, Jon Willatt, Isaac R Francis, Rodney H Reznek

Abstract readReview
In one paragraph

Review in Cancer imaging : the official publication of the International Cancer Imaging Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Prediction of 2-[Cancers · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cross-sectional imaging work-up of adrenal masses.World journal of radiology · 2013
    Article
  11. Article
  12. Multiparametric PET/CT in oncology.Cancer imaging : the official publication of the International Cancer Imaging Society · 2012
    Review
  13. Review
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

4 authors.

Anju SahdevDepartment of Radiology, St Bartholomew's Hospital, Dominion House, 59 Bartholomew's Close, London, EC1A 7ED, UK. anju.sahdev@bartsandthelondon.nhs.uk
Jon Willatt
Isaac R Francis
Rodney H Reznek

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the increasing use of abdominal cross-sectional imaging, incidental adrenal masses are being detected more often. The important clinical question is whether these lesions are benign adenomas or malignant primary or secondary masses. Benign adrenal masses such as lipid-rich adenomas, myelolipomas, adrenal cysts and adrenal haemorrhage have pathognomonic cross-sectional imaging appearances. However, there remains a significant overlap between imaging features of some lipid-poor adenomas and malignant lesions. The nature of incidentally detected adrenal masses can be determined with a high degree of accuracy using computed tomography (CT) and magnetic resonance imaging (MRI) alone. Positron emission tomography (PET) is also increasingly used in clinical practice in characterizing incidentally detected lesions. We review the performance of the established and new techniques in CT, MRI and PET that can be used to distinguish benign adenomas and malignant lesions of the adrenal gland.

Indexed as

AdenomaAdrenal Gland NeoplasmsAdrenal GlandsAdultBiopsyFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPositron-Emission TomographyTomography, X-Ray Computed

Identifiers

PMID20299300
PMCPMC2842175

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.