Evidence map›Paper›PMID 28400389›Full record

ArticleBMJ case reports2017

Hereditary leiomyomatosis and renal cell cancer (HLRCC): cutaneous and renal manifestations requiring a multidisciplinary team approach.

Agnieszka Adams, Kendall Katie Sharpe, Peter Peters, Michael Freeman

Abstract readCase Reports
In one paragraph

Article in BMJ case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Reed's Syndrome.Indian journal of dermatology
    Article
  4. Hereditary leiomyomatosis and renal cell cancer syndrome - case report and review of the literature.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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 at 3 institutions in 1 country.

Agnieszka AdamsRoyal Australian College of General Practitioners, Graceville, Australia.
Kendall Katie SharpeDepartment of Otolaryngology, Sir Charles Gairdner Hospital, Nedlands, Australia kendycakes@hotmail.com.
Peter PetersGold Coast University Hospital, Gold Coast, Australia.
Michael FreemanDepartment of Dermatology, Gold Coast Hospital and Health Service, Southport, Australia.
Gold Coast Hospital · AURoyal Australian College of General Practitioners · AUSir Charles Gairdner Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous leiomyomasare rare tumours of smooth muscle origin associated with disorders such as hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome. HLRCC is an autosomal dominant syndrome caused by loss of function mutations in the fumarate hydratase gene. Sufferers of this disorder are predisposed to the development of tumours of the skin and/or uterus, with a further subset of HLRCC families at risk of renal cell carcinoma with papillary features. This syndrome is rare and carries with it a significant rate of mortality. A multidisciplinary approach to care is critical in the management of these patients and their families. The dermatologist can play a central role in this process, coordinating care between specialist medical and allied health teams.

Indexed as

MutationAdultDisease ManagementFumarate HydrataseGenetic CounselingHumansLeiomyomatosisMaleNeoplastic Syndromes, HereditarySkin NeoplasmsUterine NeoplasmsFumarate HydrataseDermatologyObstetrics and gynaecologyUrology

Identifiers

PMID28400389
PMCPMC5543308
OpenAlexW2619687601

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.